LIST OF TITLES
A "new" chromosome marker common to the Rett syndrome and infantile autism? The frequency of fragile sites at X P22 in 81 children with infantile autism, childhood psychosis and the Rett syndrome.
A 77-year-old woman and a preserved speech variant among the Danish Rett patients with mutations in MECP2
A belated diagnosis
A biogenic amine-synapse mechanism for mental retardation and developmental disabilities
A boy with Rett syndrome?
A Brazilian girl with the Rett syndrome
A candidate gene for Rett syndrome: Search for mutations in the UBE2A gene
A case of effective gastrostomy for severe abdominal distention due to breathing dysfunction of Rett's syndrome: a treatment of autonomic disorder
A case of massive gastric necrosis in a young girl with Rett syndrome
A case of multiple congenital anomalies in association with Rett syndrome confirmed by MECP2 mutation screening
A case of ornithine transcarbamylase deficiency with Rett syndrome manifestations
A case of Rett syndrome
A case of Rett syndrome from Ukraine--clinical diagnosis confirmed by mutation analysis of the MECP2 gene
A case of Rett syndrome phenotype in male
A case of the Rett syndrome
A case of the Rett syndrome with acute encephalopathy induced during calcium hopantenate treatment
A case of trisomy 22 in Pongo pygmaeus
A case of variant Rett syndrome with unusual neuropathological findings
A cerebral atrophic syndrome in hypoammoniemia [Translation]
A chemist's dream researcher's daughter inspires charity 2,348-mile kayak/canoe race for Rett syndrome
A chorea kinship with rigid form [Translation]
A clinical scale for determining the sensitivity of MECP2 genetic analysis [Translation]
A comparative study of X-inactivation in Rett syndrome probands and control subjects
A contribution regarding the Rett syndrome
A contribution regarding the Rett syndrome. The first observation of a female patient in the German Democratic Republic [Translation]
A De Novo X:3 translocation in Rett syndrome
A detailed analysis of the MECP2 gene: prevalence of recurrent mutations and gross DNA rearrangements in Rett syndrome patients
A double blind trial of bromocriptine in the Rett syndrome
A forest can hide a tree Rett syndrome: a second genetic cause of mental retardation in young girls? [Translation]
A girl with features of two X-linked dominant disorders: Rett syndrome and incontinentia pigmenti.
A glossary of genetic terms
A home of her own
A kink in their and in our existence. Aspects of giving sense regarding children with Rett syndrome [Translation]
A kink in your existence [Translation]
A longitudinal study of cognitive skills and communication behaviours in children with Rett syndrome
A low-cost method for simultaneous video-recording of ambulant subject and electroencephalograph: the quarrier's system
A medical team approach
A model for the inheritance of Rett syndrome
A monozygotic twin pair with Rett syndrome
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos
A mutation in the Rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males
A naturalistic open-label study of mirtazapine in autistic and other pervasive developmental disorders
A new assay for the analysis of X-chromosome inactivation in carriers with an X-linked disease
A new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion map
A new type of neuronal ceroid-lipofuscinosis (NCL) mimicking Rett's syndrome (RS)
A nonsense mutation in the a4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBN 1)
A novel protein, xenopus p20, influences the stability of MeCP2 through direct interaction
A paradigmatic shift in the approach to neuropsychiatric gene linkage may require an anthropogenetic perspective
A parent's experience of scoliosis surgery
A polygraphic and neuroendocrinological study of the Rett syndrome
A population-based approach to the investigation of osteopenia in Rett syndrome
A portrait of Andreas Rett
A prevalence study of Rett syndrome in an institutionalised population
A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome
A program for training children with Rett syndrome
A progressive syndrome of autism, dementia, ataxia and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases
A rare hand malformation, the Freeman-Sheldon syndrome [Translation]
A Rett patient with a typical Angelman EEG
A Rett syndrome MECP2 mutation that causes mental retardation in men
A Rett syndrome patient with a ring X chromosome: further evidence for skewing of X inactivation and heterogeneity in the aetiology of the disease
A review of Rett syndrome: stressing successful educational intervention
A review of the biochemical pathways studied and abnormalities reported in the Rett syndrome
A review of the respiratory disorder in the Rett syndrome
A review of the Rett syndrome with a theory of autism
A search for uniparental disomy as a cause of Rett syndrome
A search for X-chromosome uniparental disomy and DNA rearrangements in the Rett syndrome
A set of monozygotic twins with Rett syndrome
A severely affected male born into a Rett syndrome kindred supports X-linked inheritance and allows extension of the exclusion map
A study of the natural history of Rett syndrome in 23 girls
A study on the Rett syndrome in the German Democratic Republic
A teacher’s perspective
A touch of hands. A cookbook to benefit the International Rett Syndrome Association
A transcriptional repressor MeCP2 causing Rett syndrome is expressed in embryonic non-neuronal cells and controls their growth
A view of scoliosis
A view on care and management
A view on care and management [Translation]
A view on water-based activities with a Rett child
A WW domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndrome
AAC instruction for children with Rett syndrome using assistive technology
Aberrant sleep patterns in children with the Rett syndrome
Abilities and needs of children with Rett syndrome
Abnormal breathing in the Rett syndrome
Abnormal carbohydrate metabolism in cerebrospinal fluid in Rett syndrome
Abnormal cortical excitability in Rett syndrome
Abnormal development of biceps brachii phasic stretch reflex and persistence of short latency heteronymous reflexes from biceps to triceps brachii in spastic cerebral palsy
Abnormal early infantile development in Rett syndrome: expanding the criteria for MECP2 testing
Abnormal expression of microtubule-associated protein 2(MAP-2) in neocortex in Rett syndrome
Abnormal general movements in girls with Rett disorder: The first four months of life
Abnormal methylation of a MECP2 mutant allele in a boy with “male Rett syndrome” and his unaffected heterozygous mother
Abnormal methylation of a MECP2 mutant allele in a boy with “male Rett syndrome” and his unaffected characteristic X-ray sign of Rett syndrome: extreme thin diaphysis with narrow medulla of tubular bones
Abnormal mitochondria in Rett syndrome: one case report
Abnormal mitochondria in the Rett syndrome
Abnormalities in neuronal maturation in Rett syndrome neocortex: molecular correlates
Abnormalities in neuronal maturation in Rett syndrome neocortex: preliminary molecular correlates
Abnormalities in urinary pterin levels in Rett syndrome
Abnormalities of carbohydrate metabolism and of OCT gene function in the Rett syndrome
Abnormalities of social interactions and home cage behavior in a mouse model of Rett syndrome
Abnormalities of thyroid function and glucose control in subjects with Rett syndrome
Absence of MeCP2 mutations in patients from the South Carolina autism project
Abstracts congress ' 93
Account of the research programme in the Rett Syndrome [Translation]
Additional clinical and cytogenetic findings associated with Rett syndrome
Adjunct diagnostic test for Angelman syndrome: the tuning fork response
Administration of trimeprimine in pediatrics [Translation]
Advance made in understanding Rett's syndrome
Advice to parents of young girls with Rett syndrome: getting started with reading and communication
After 30 years, Rett syndrome remains an enigma
Age-related occurrence of signs and symptoms in the Rett syndrome
Agyria-pachygyria (lissencephaly syndrome)
Air swallowing in Rett syndrome
Airbloat in Rett syndrome and its association with multiple swallowing during resting apnoea
Airflow obstruction in children with Rett Syndrome
Alterations in dopaminergic function in Rett syndrome
Alterations in replication timing of X-chromosome bands in Rett syndrome
Altered cerebellar ganglioside pattern In Rett syndrome
Altered cholinergic function in the basal forebrain of girls with Rett syndrome
Altered CSF ganglioside pattern - A biological marker of Rett syndrome
Altered development of glutamate and GABA receptors in the basal ganglia of girls with Rett syndrome
Altered dopaminergic receptor binding sites in the caudate nucleus of subjects with Rett syndrome
Altered energy balance may account for growth failure in Rett syndrome
Altered methylation pattern of the G6 PD promoter in Rett syndrome
Altered neurochemical markers in Rett’s syndrome
Ambulation in Rett syndrome
Amino acid receptor studies in Rett syndrome
An analogue assessment of hand stereotypies in two cases of Rett syndrome
An analogue assessment of repetitive hand behaviours in girls and young women with Rett syndrome
An effective computer-based requesting system for persons with Rett syndrome
An HPLC-linked assay of phosphoribosylpyrophosphate synthetase activity in the erythrocytes of adults and children with neurological disorders
An introduction to Rett syndrome
An investigation into the communication needs of girls with Rett syndrome, with consideration of posible approaches to a design solution
An update on clinically applicable diagnostic criteria in Rett syndrome. Comments to Rett Syndrome Clinical Criteria Consensus Panel Satellite to European Paediatric Neurology Society Meeting, Baden Baden, Germany, 11 September 2001
Anaesthesia and Rett syndrome: a case report
Anaesthesia for Rett syndrome
Analysis of aberrant behaviour associated with Rett syndrome
Analysis of deletions of the MECP2 gene in Rett's syndrome (RTT) and Rett's syndrome "plus" (RTT+) patients
Analysis of gait in the girl with Rett syndrome: a case study [Translation]
Analysis of glial fibrillary acidic protein in the cerebrospinal fluid of children investigated for encephalopathy
Analysis of mutations of the MECP2 gen in patients with Rett syndrome [Translation]
Analysis of the genomic structure of the human glycine receptor 2 subunit gene and exclusion of this gene as a candidate for Rett syndrome
Analysis of the most frequent mutations in girls with Rett syndrome[Translation]
Analysis of the X-chromosome in Rett syndrome
Anatomy of Rett syndrome
Anesthesia in a child with Rett syndrome: a case report and literature review
Angelman syndrome phenotype associated with mutations in MECP2, a gene encoding a methyl CpG binding protein
Angelman syndrome: Mimicking conditions and phenotypes
Angelman’s Syndrome
Animal models of mental retardation: from gene to cognitive function
Annexin-1 is abnormally expressed in Fragile X syndrome: Two-dimensional electrophoresis study in lymphocytes
Annual general meeting
Another model for the inheritance of Rett syndrome
Another patient with MECP2 mutation without classic Rett syndrome phenotype
Another Rett patient with a typical Angelman EEG
Anti-Alfal Tubulin autoantibodies in Rett syndrome patients
Antibodies to nerves growth factor in children with nervous system maldevelopment
Anti-neural autoantibodies in Rett syndrome patients
Anxiety disorders in the fourth edition of the classification of mental disorders prepared by the American Psychiatric Association: diagnostic and statistical manual of mental disorders (DMS-IV -- options book) [Translation]
Applications of transcranial magnetic stimulation in movement disorders
Apraxia and motor control disorders in Rett syndrome: a longitudinal study in the first decade of life
Aquatic rehabilitation in Rett syndrome
Ask the experts: questions and answers
Ask the experts: questions and answers
Aspects on origin - future approach
Assessing refraction in children with cerebral damage [Translation]
Assessing the development level in Rett syndrome
Assessing the development level of Rett syndrome girls
Assessment and intervention of hand behaviors
Assessment and management of feeding problems in individuals with Rett syndrome: results from a population of clinic attenders
Assessment and management of females with Rett syndrome
Assessment and treatment of a girl with Rett syndrome
Assessment of potential communicative acts in three individuals with Rett sndrome
Assessment of preference for varied versus constant reinforcers
Assessment of the maturity-related brainstem functions reveals the heterogeneous phenotypes and facilitates clinical management of Rett syndrome
Association by guilt: identification of DLX5 as a target for MeCP2 provides a molecular link between genomic imprinting and Rett syndrome
Associations between MeCP2 mutations, x-chromosome inactivation, and phenotype
Associative learning in Rett girls: an explorative study, theory and assessment
Attention-deficit hyperactivity disorder (ADHD) and frontal-motor cortex disconnection
Atypical forms of Rett syndrome
Atypical forms of Rett's syndrome [Translation]
Auditory brainstem response findings in Rett syndrome
Auditory brainstem response findings in Rett syndrome: stability over time
Auditory brainstem responses in Rett syndrome: effects of hyperventilation, seizures, and tympanometric variables
Auditory evoked potentials in Rett syndrome
Auditory processing deficit in a patient with Rett syndrome
Augmentative alternative communication in Rett syndrome [Translation]
Augmentative communication: applications and practical strategies for children who have Rett syndrome
Augmentative communications for consumers
Augmentative communications for educators
Autism and Rett syndrome - Pedopsychiatric aspects [Translation]
Autism and Rett syndrome: behavioural investigations and differential diagnosis
Autism and Rett syndrome: some notes on differential diagnosis
Autism as a neurodevelopmental disorder affecting communication and learning in early childhood: prenatal origins, post-natal course and effective educational support
Autism screening questionnaire: diagnostic validity
Autism under age 3 years: a clinical study of 28 cases referred for autistic symptoms in infancy
Autistic and dysphasic children I: Clinical characteristics
Autistic and dysphasic children II: Epilepsy
Autistic spectrum disorders: clinical presentation in preschool children
Autistic symptoms in Rett syndrome: the first 2 years according to mother reports
Autistic traits in the Rett syndrome
Autoantibodies to nerve growth factor and astroglial protein S-100 in Rett's syndrome [Translation]
Autoimmune mechanisms in the genesis of developmental abnormalities of the nervous system [Translation]
Automated Talairach atlas-based parcellation and measurement of cerebral lobes in children
Autonomic dysfunction and sudden death in Rett syndrome
Autonomic dysfunction in mental retardation and spastic paraparesis with MECP2 mutation
Autonomic function in a girl with Rett syndrome
Award of the Peter Emil Becker Prize 2000 to Prof. Bengt Hagberg, Gothenburg
Balanced X chromosome inactivation patterns in the Rett syndrome brain
Basic movement for profoundly handicapped children
Basics of music therapy and music psychology [Translation]
Been there, done that: creating a situation that works
Behavior problems in adult women with Rett syndrome
Behavioral competition in a case of Rett syndrome
Behavioral observations concerning differential diagnosis between the Rett syndrome and autism
Behavioral stereotypes in the Rett syndrome [Translation]
Behavioral training of a young women with Rett syndrome
Behavioral treatment of Rett's disorder: ineffectiveness in three cases
Behavioral treatment of sleep dysfunction in patients with the Rett syndrome
Behaviour in the Rett disorder
Behaviour phenotypes [Translation]
Behavioural and emotional features in Rett syndrome
Behavioural and emotional features of Rett syndrome
Behavioural and emotional features of Rett syndrome
Behavioural phenotypes. Biologically determined neuropsychological patterns [Translation]
Benefits for Rett girls
Benign familial neonatal convulsions; psychosocial adjustment to the threat of recurrent seizures
Bibliography and abstract bibliography on Rett syndrome
Bibliography of medical literature from medicine 88-july 93
Bibliography. Current world literature. Developmental disorders
Biochemical and clinical effects of tyrosine and tryptophan in the Rett syndrome
Biochemical studies in Rett syndrome: the search for a diagnostic marker
Biochemical studies of oxidative metabolism in Rett syndrome
Biogenic amines in the Rett syndrome
Biological basis of Rett syndrome [Translation]
Biometrical aspects of Rett syndrome: growth (head), weight, height, energy expenditure
Biotin and Rett syndrome
Body composition of Hungarian Rett syndrome girls
Bone histomorphometry in three females with Rett syndrome
Bone quality and its effects in Rett syndrome
Bone turnover and skeletal status in patients with Rett syndrome
Book review on Rett Syndrome- Clinical and Biological Aspects, ed. by Hagberg, Anvret and Wahlstrom
Brain damage from blood group incompatibility [Translation]
Brain glucose metabolism in Rett syndrome
Brain MR imaging (MRI), MR spectroscopy (MRS), and TC99M-ethyl-cysteinate dimer single photon emission tomography (TC99MECD-SPET) in Rett syndrome
Brain MR imaging in neonatal hyperammonemic encephalopathy resulting from proximal urea cycle disorders
Brain perfusion abnormalities in Rett syndrome: a qualitative and quantitative SPET study with ^9^9Tc^m-ECD
Brain perfusion SPECT and EEG findings in Rett syndrome
Brain plasticity in paediatric neurology
Brain-directed autoantibodies levels in the serum of Rett syndrome patients
Brainstem and spinal cord impairment in Rett syndrome: somatosensory and auditory evoked responses investigations
Brainstem frequency-following responses in Rett syndrome
Breaking the silence in Rett syndrome
Breathing and movement difficulties in Rett syndrome
Breathing disorders in males with acquired encephalopathy
Breathing impairment in central alveolar hypoventilation and Rett syndrome
Breathing impairment in Rett syndrome
Bridges - A book of hope and inspiration for families
Brief report: autistic behaviors among children with fragile X or Rett syndrome: implications for the classification of pervasive developmental disorder
Brief report: cognitive and adaptive functioning in 28 girls with Rett syndrome
Brief report: fostering environmental control in a young child with Rett syndrome: a case study
Brief report: neuroanatomic observations of the brain in pervasive developmental disorders
Brief report: non-random X chromosome inactivation in females with autism
Brief report: two sisters with Rett syndrome
Brief research communication: additional clinical and cytogenetic findings associated with Rett syndrome
Bromocriptine improves circadian rhythm in Rett syndrome [Translation]
Bromocriptine in the Rett syndrome
Bruxism in Rett syndrome: a case report
Buspirone in Rett syndrome respiratory dysfunction
Calcium absorption is normal in girls with Rett syndrome
Calorie boosters and diet tips
Can hand function be maintained and improved through occupational therapy?
Can we relate MeCP2 deficiency to the structural and chemical abnormalities in the Rett brain?
Candidate gene analysis in Rett syndrome and the identification of 21 SNPs in Xq
Cardiac dysautonomia and serotonin plasma levels in Rett syndrome
Care of spine of carers caring for Rett syndrome girls/women
Care today / cure tomorrow
Carnitine deficiency and carnitine therapy in a patient with Rett syndrome [Translation]
Carolyn’s genetics cookbook
Cause, appearances, possibilities and limits of progress in a child with Rett syndrome [Translation]
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome
CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasms
Celebrity appeals for research dollars "intensifying" in USA
Cerebellar and cerebral abnormalities in Rett syndrome: A quantitative magnetic resonance (MR) analysis
Cerebral atrophic syndrome in hyperammonemia in children [Translation]
Cerebral atrophy with hyperammonaemia
Cerebral blood flow and oxygen metabolism in Rett syndrome
Cerebral blood flow and oxygen metabolism in Rett syndrome [Translation]
Cerebral blood flow and oxygen metabolism in the Rett syndrome
Cerebral blood flow in Rett syndrome: evaluation with continuous arterial spin labeling
Cerebral folate deficiency
Cerebral folate deficiency syndrome
Cerebral lateralisation and rate of maturation
Cerebral magnetic resonance spectroscopy in Rett syndrome. Failure to detect mitochondrial disorder
Cerebral oxygenation and hemodynamics during hyperventilation and sleep in patients with Rett syndrome
Cerebral oxygenation during hyperventilation and sleep in Rett patients investigated by near infrared spectroscopy
Cerebral proton magnetic resonance spectroscopy in Rett syndrome
Cerebrolysin therapy in Rett syndrome: clinical and EEG mapping study
Cerebrospinal B-endorphins and biogenic amines
Cerebrospinal biogenic amines in Rett syndrome
Cerebrospinal fluid B-endorphin and cortisol study in Rett syndrome
Cerebrospinal fluid B-endorphin in Rett syndrome
Cerebrospinal fluid biogenic amines and biopterin in Rett syndrome
Cerebrospinal fluid biopterin in Rett syndrome [Translation]
Cerebrospinal fluid concentration of homovanillic acid and 5-hydroxyindoleacetic acid in patients with Rett syndrome
Cerebrospinal fluid gangliosides in patients with Rett syndrome and infantile neuronal ceroid lipofuscinosis
Cerebrospinal fluid levels of substance P in patients with Rett syndrome
Cerebrospinal fluid studies in the Rett syndrome: biogenic amines and beta-endorphins
Cerebrospinal fluid values for monoamine metabolites, gamma-aminobutyric acid, and other amino compounds in Rett syndrome
Changes in excitatory and inhibitory neurotransmitter receptors in Rett syndrome and a mouse model for Rett syndrome
Changing criteria of autistic disorders: a comparison of the ICD-10 research criteria and DSM-IV with DSM-III-R, CARS, and ABC
Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder
Characterisation of seizures in Rett syndrome
Characteristic patterns of dendritic protein expression in Down syndrome and Rett syndrome
Characteristic response to transcranial magnetic stimulation in Rett syndrome
Characteristics of motor disturbances of the Rett syndrome
Chilaiditi's colon interposition in a patient with Rett syndrome [Translation]
Children and adults with infantile autism [Translation]
Children in our hand - A life with disabled people [Translation]
Children with Rett syndrome and their parents. A research on the internet [Translation]
Children with Rett syndrome: on the situation of their families [Translation]
Children with special needs - Rett syndrome
Children, youth and grown-ups with Rett Syndrome. Disability and special needs [Translation]
Chiropractic
Choline acetyltransferase activity and vesamicol binding in Rett syndrome and in rats with nucleus basalis lesions
Cholinergic regulation of cortical development and plasticity. New twists to an old story
Choosing residential care - some questions
Chromatographic profiles at E-280 nm for urinary precipitates in morbus Rett
Chromosomal fragility, structural rearrangements and mobile element activity may reflect dynamic epigenetic mechanisms of importance in neurobehavioural genetics
Chromosomal mapping of the human M6 genes
Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like features
Chromosome findings in the Rett syndrome and a test of a two-step mutation theory
Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq
Chromosome studies in 10 patients with the Rett syndrome
Circulatory regulation disorders in children with brain damage [Translation]
Classic Rett syndrome in a boy as a result of somatic mosaicism for a MECP2 mutation
Classic Rett syndrome in a boy with R133C mutation of MECP2
Classical Rett syndrome girl with "Forme Fruste" variant maternal aunt
Classical Rett syndrome in Australia
Classical Rett syndrome in sisters: variability of clinical expression
Clinical analysis in nine Brazilian cases of the Rett syndrome
Clinical analysis of male cases with hand-washing-like stereotypes similar to those in Rett syndrome
Clinical and anthropological studies of Rubinstein-Taybi syndrome [Translation]
Clinical and electroencephalographic results in Rett syndrome [Translation]
Clinical and electroencephalographical study of Rett syndrome
Clinical and molecular genetic findings in four girls with Rett syndrome [Translation]
Clinical and psychological axis symptoms of brain damage in children [Translation]
Clinical and psychological studies on the effect of vascular and metabolic active substances on the cerebral circulation in children with brain damage [Translation]
Clinical and ultrastructural studies in a girl with progressive spastic ataxia and stereotyped motor behavior - Rett's syndrome
Clinical assessment of Rett syndrome in Bulgaria
Clinical course of epileptic seizures in Rett's syndrome [Translation]
Clinical criteria, stages and natural history
Clinical delineation of Rett syndrome variants
Clinical disorders of brain plasticity
Clinical experts on Rett disorder
Clinical feature of Rett syndrome and MeCP2 genotype/phenotype correlation analysis [Translation]
Clinical features of the early stage of the Rett syndrome
Clinical genetics: Rett syndrome [Translation]
Clinical heterogeneity of the autistic syndrome: a study of 60 families [Translation]
Clinical manifestations and stages of Rett syndrome
Clinical phenotypes of classic Rett syndrome [Translation]
Clinical presentations and biochemical investigations in 32 patients with Rett syndrome
Clinical profile of a male with Rett syndrome
Clinical psychological studies on adolescent and adult mongols [Translation]
Clinical recognition and differential diagnosis of Rett syndrome
Clinical recognition of Rett syndrome
Clinical studies of oxidative metabolism in Rett syndrome
Clinical studies of pervasive developmental disorders in Japan
Clinical study of 13 cases of Rett syndrome [Translation]
Clinical study of four cases of Rett syndrome [Translation]
Clinical symptoms of the Rett syndrome patients with MECP2 gene abnormalities [Translation]
Clinical trials and treatment prospects
Clinical variability in Rett syndrome
Clinical variability within consanguinity in Rett syndrome
Clinical, neurophysiological and differential diagnostic aspects of severe early childhood autism [Translation]
Clinical, neurophysiological and immunological correlations in classical Rett syndrome
Clinical, symptomatological, psychological and metabolic problems in Rett syndrome. Proceedings of the 24th international symposium of the Ludwig Boltzmann Institute for research on infantile brain damages, Vienna, September 26-27, 1984
Clinico-biochemical variants of Rett syndrome in children
Closely related Swedish Rett syndrome females - none with mecp2 mutation revealed
Closing remarks
Cognitive profile of Rett syndrome
Colonic lymphoid hyperplasia in melanosis coli
Comment on Rett syndrome and genetic drift, Buhler et al.
Commentary: potential neurobiologic mechanisms through which metabolic disorders could relate to autism
Commentary: the challenge of Rett syndrome
Commitment to X inactivation precedes the twinning event in monochorioic MZ twins
Common origins in Rett's syndrome
Communication
Communication abilities and Rett syndrome
Communication abilities in a case of Rett syndrome
Communication and feeding in Rett syndrome [Translation]
Communication and oral-motor function in Rett syndrome
Communication and oral-motor function in the Rett syndrome
Communication in Rett syndrome
Communication in Rett syndrome [Translation]
Communication in Rett syndrome and research review
Communication in Rett syndrome complex
Communication in Rett syndrome with client assessment of a 12-year old [Translation]
Communication skills among females with Rett syndrome
Communication training in education for girls with Rett syndrome [Translation]
Communication with the eye, especially in relationship to a girl with Rett syndrome [Translation]
Comparative effects of bilateral hand splints and an elbow orthosis on stereotypic hand movements and toy play in two children with Rett syndrome
Comparative study of methyl-CpG-binding domain proteins
Completely skewed X-inactivation in a mentally retarded young female with pseudohypoparathyroidism type IB and juvenile renin-dependent hypertension
Computer aided two-dimensional electrophoretic gel analysis
Computer use in Rett syndrome
Computerized ribosomal RNA secondary structure modeling of mutants found in Rett syndrome patients and their mothers [Translation]
Concluding remarks on the preceding comment by W. Lenz [Translation]
Condensed points for diagnostic criteria and stages in Rett Syndrome
Confocal laser scanning microscopy and 3-D reconstructions of neuronal structures in human brain cortex
Congenital variant Rett syndrome in a girl with terminal deletion of chromosome 3p
Constipation
Constipation as a clinico-therapeutic problem of brain-damaged children [Translation]
Constipation: advice on massage and aromatherapy
Contemporary views on Rett's syndrome: clinical, cytogenetic and molecular studies [Translation]
Contribution to studies of seizures in Rett's syndrome. Analysis of critical forms of four cases [Translation]
Control, communication, and computers: providing girls with Rett syndrome increased access to the environment
Controversies in the treatment of autistic children: vitamin and drug therapy
Coping and renewing (a useful pamphlet for parents and carers)
Coping with challenge
Coping with Rett syndrome
Correlation of electroencephalogram, respiration and movement in the Rett syndrome
Correlation of stereotypic hand movements and Rolandic EEG spikes
Cortical development in Rett syndrome: molecular, neurochemical and anatomical aspects
Cortical reflex myoclonus in Rett syndrome
Cough as a main symptom and its treatment [Translation]
Courage to care: seven families touched by disability
Cranial computed tomographic and magnetic resonance imaging studies on the Rett syndrome
Creatine monohydrate increases strength in patients with neuromuscular disease
Critical consideration on the use of psychopharmacological agents in children [Translation]
CRSA Newsletter
Crying spells in Rett syndrome
CSF and urine biogenic amine metabolites in Rett syndrome
CSF B-endorphin levels in patients with infantile autism
CSF beta-endorphin levels in pediatric neurologic disorders
CSF beta-endorphins in childhood neuropsychiatric disorders
CSF ganglioside analysis using a highly sensitive enzyme-immunostaining method in Rett syndrome and other neurologic diseases
Current approaches to the problem of autism in childhood [Translation]
Current neuropediatric aspects: the extraordinary "saga" of Rett's syndrome [Translation]
Current news on the Rett syndrome [Translation]
Current problems in diagnosis and treatment of hereditary disturbances of growth and development in children [Translation]
Current research projects
Current status of genetic research in Rett syndrome
Cyclooxygenase-2 expression during rat neocortical development and in Rett syndrome
Cytogenetic and molecular-cytogenetic investigation of Rett syndrome: analysis of 31 cases
Cytogenetic and molecular-cytogenetic studies of Rett syndrome (RTT): a retrospective analysis of a Russian cohort of RTT patients (the investigation of 57 girls and three boys).
Cytogenetic and molecular-genetic diagnostics of Rett syndrome in children [Translation]
Cytogenetic study of patients with Rett syndrome [Translation]
Cytoskeletal protein and excitatory amino acid receptor development in a potential mouse model for Rett Syndrome
Day to day care of Rett syndrome children
De novo MECP2 frameshift mutation in a boy with moderate mental retardation, obesity and gynaecomastia
De novo MECP2 mutation in a 46,XX male patient with Rett syndrome
Debate and argument: having Rett syndrome in the ICD-10 PDD category does not make sense
Debate and argument: there are connections between brain and mind and it is important that Rett syndrome be classified somewhere
Decrease in benzodiazepine receptor binding in the brains of adult patients with Rett syndrome
Decreased benzodiazepine receptor binding in the brain of adult Rett patients
Decreased cerebrospinal fluid levels of beta-phenylethylamine in patients with Rett syndrome
Decreased cerebrospinal fluid levels of substance P in patients with Rett syndrome
Decreased dendritic branching in frontal, motor and limbic cortex in Rett syndrome compared with trisomy 21
Decreased glutamate receptor density in the basal ganglia in Rett syndrome
Defect in normal developmental increase of the brain biogenic amine concentrations in the mecp2-null mouse
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
Degenerative central nervous system (CNS) disease
Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice
Deletion of exons 3 and 4 of MECP2 gene, revealed by MLPA technique, in a RTT italian girl with "classical" phenotype
Deletion screening by fluorescence in situ hybridization in Rett syndrome patients
Demonstration of specific heterochromatic segments in the orangutan (pongo pygmaeus) by a distamycin/DAPI double staining technique
Denaturing high-performance liquid chromatography and sequence analyses for MECP2 mutations in Rett syndrome
Dendritic anomalies in disorders associated with mental retardation
Dendritic cytoskeletal protein expression in mental retardation: an immunohistochemical study of the neocortex in Rett syndrome
Dental care of brain damaged children--a clinical and social problem [Translation]
Dental considerations of handicapped and retarded children [Translation]
Dental health for people with handicaps including Rett syndrome
Dental problems in brain damaged children [Translation]
Derepression of BDNF transcription involves calcium-dependent phosphorylation of MeCP2
Dermatoglyphic studies in Rett syndrome
Dermatoglyphs in Rett syndrome [Translation]
Describing the phenotype in Rett syndrome using a population database
Detailed physical mapping and overlap YAC cloning in the region containing the X chromosome breakpoint from a patient with an X;3 translocation and the Rett syndrome phenotype.
Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD-PCR)
Developing a computer program for enhancing symbol recognition by girls with Rett syndrome
Developing literacy skills
Developing the Individual Education Plan (IEP)
Development of a Rett syndrome checklist
Development of amino acid receptors in frontal cortex from girls with Rett syndrome
Development of language in Rett syndrome
Developmental aspects of cerebrospinal fluid levels of beta- phenylethylamine and it's role in pediatric neurological disorders
Developmental disorder in girls due to Rett syndrome [Translation]
Developmental disorders in the fourth edition of the American classification: diagnostic and statistical manual of mental disorders (DSM IV -- optional book) [Translation]
Developmental disorders of activity dependent neuronal plasticity
Developmental expression of methyl-CpG binding protein 2 is dynamically regulated in the rodent brain
Developmental profile of serum nerve growth factor levels in Rett complex
Developmental psychology of genetic syndromes [Translation]
Developmental regression in autism spectrum disorders
Developments of girls with Rett syndrome. An exploring inquiry into temperament and characteristics of girls with the Rett syndrome
DHPLC analysis of the MECP2 gene in Italian Rett patients
DHPLC as a method for high throughput, cost effective mutation screening: application for Rett syndrome
Diabetes mellitus type 1: association with Rett syndrome
Diagnosis and treatment of Rett syndrome
Diagnosis of degenerative disorders of the nervous system by ultrastructural analysis of extracerebral biopsies [Translation]
Diagnosis of Rett syndrome in view of own observations in the group of 100 girls
Diagnosis of Rett syndrome: can a radiograph help?
Diagnosis: Rett syndrome - and then? More self-determination through alternative communication [Translation]
Diagnostic chorionic biopsies in the first trimester. Report of experiences over a 2 year period [Translation]
Diagnostic criteria for Rett syndrome
Diagnostic criteria of autism and Asperger's syndrome: similarities and differences [Translation]
Diagnostic DHPLC Quality Assurance (DDQA): a collaborative approach to the generation of validated and standardized methods for DHPLC-based mutation screening in clinical genetics laboratories
Diagnostic features of autism
Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms
Difference between plasma N- and C-terminally directed beta-endorphin immunoreactivity in infantile autism
Difference in early development of presumed monozygotic twins with Rett syndrome
Differential diagnosis of symptoms with abnormal respiration (tachypnea-apnea)
Differential diagnosis of the Rett syndrome and autistic syndromes
Differential gene expression in human postmortem Rett syndrome brain revealed by cDNA microarray
Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype-phenotype associations in Rett syndrome
Direct evidence for skewed X-chromosome inactivation in Rett syndrome by combination of FISH and BrdU+Hoechst staining techniques
Disability influencing the ability to learn and act [Translation]
Disability living allowance-Mobility allowance
Discovery of a new protein isoform of MeCP2 and exon 1 mutations causing Rett syndrome
Discovery of the Rett syndrome and its function [Translation]
Discovery of the Rett syndrome gene and its function
Discussant - pathophysiologies of Rett syndrome
Discussion for the Rett Syndrome symposium--the importance of rigorously defining one's level of investigation
Diseases of the mind and brain: Rett's syndrome
Diseases of the mind and brain: Rett's syndrome, Part II
Disorganized rhythm and synchrony: early signs of autism and Rett syndrome
Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndrome
Distinct expression profiles of Mecp2 transcripts with different lengths of 3'UTR in the brain and visceral organs during mouse development
Disturbance of phasic chin muscle activity during rapid-eye-movement sleep
DNA binding selectivity of MeCP2 due to a requirement for A/T sequences adjacent to methyl-CpG
DNA methylation and histone deacetylation in the control of gene expression: basic biochemistry to human development and disease
DNA methylation and Rett syndrome
DNA methylation in health and disease
DNA methylation protocols. Overview
DNA methylation, histone deacetylase repressory complexes and development
DNA methylation, nuclear structure, gene expression and cancer
DNA methylation-related chromatin remodeling in activity-dependent BDNF gene regulation
DNA recognition by the methyl-CpG binding domain of MeCP2
Does a legasthenia-syndrom exist? [Translation]
Does augmentative communication play a role in Rett syndrome?
Does loss of motor skills mean irreversible deterioration?
Does transcranial magnetic stimulation allow early diagnosis of Rett syndrome?
Dopamine re-uptake inhibitor GBR-12909 induction of aberrant behaviors in animal models of dopamine dysfunction
Dopamine transporter changes in neuropsychiatric disorders
Dopamine transporters are markedly reduced in Lesch-Nyhan disease in vivo
Dopaminergic D2 receptor SPECT imaging in Rett syndrome: increase of specific binding in striatum
Down syndrome: MR quantification of brain structures and comparison with normal control subjects
Dual diagnoses. Psychiatric disorders in developmental disabilities
Dual X-ray absorptiometry and bone ultrasonography in patients with Rett syndrome
Duke study finds link between patients with autistic disorder and patients with Rett syndrome
Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males
Dystonia and lactic acidosis: new features of Rett's syndrome
Earlier appearance of sub-band Xp21.2 on the late replication chromosome X in Rett syndrome girl
Earlier finishing of Xp21.2 sub-band replication of the inactive X chromosome in Rett syndrome girl but not in her 47, XXX mother
Early abnormality in pterin levels in Rett syndrome
Early behavior characteristics and sleep disturbance in Rett syndrome
Early clinical signs in the Rett disorder
Early communication development in children with Rett syndrome
Early diagnosis and treatment of spastic cerebral palsy [Translation]
Early differential diagnosis of infantile neuronal ceroid lipofuscinosis, Rett syndrome, and Krabbe disease, by CT and MR
Early infant intelligence and Rett syndrome
Early monoaminergic dysfunction
Early motor disturbances in Rett syndrome and its pathophysiological importance
Early onset seizures and Rett-like features associated with mutations in CDKL5
Early seizure onset in Rett syndrome
Early stages of the Rett syndrome and infantile neuronal ceroid lipofuscinosis - A difficult differential diagnosis
Eating difficulties in girls with Rett syndrome compared with other developmental disabilities
Education and therapy: ambulant client/patient.
Education and therapy: non-ambulant client/patient
Education rights
Educational and therapeutic intervention in Rett syndrome
Educational implications of Rett syndrome
EEG abnormalities aid diagnosis of Rett syndrome
EEG and respiration in Rett syndrome
EEG development in classical Rett syndrome: a retrospective study of 75 cases
EEG development in Rett syndrome. A study of 30 cases
EEG mapping in a child with Rett syndrome
EEG mapping in girls with Rett syndrome
EEG peculiarities in girls with Rett syndrome
Effect of diazepam on apnea attacks in a 6-year-old girl with Rett syndrome: a polysomnographic study [Translation]
Effect of grafting technique on the maintenance of coronal and sagittal correction in anterior treatment of scoliosis
Effect of hand splints on stereotypic hand behaviour of girls with Rett syndrome: a replication study
Effect of hand splints on stereotypic hand behaviour of three girls with Rett syndrome
Effect of postural changes in feeding
Effect of topiramate on seizures and respiratory dysrhythmia in Rett syndrome
Effects of amount and type of social interaction/activity on stereotyped hand mannerisms in individuals with Rett syndrome
Effects of MECP2 mutation type, location and X-inactivation in modulating Rett syndrome phenotype
Effects of Rett syndrome mutations of the methyl-CpG binding domain of the transcriptional repressor MeCP2 on selectivity for association with methylated DNA
Efficacy of Vigabatrin on seizures of Rett syndrome [Translation]
Electrocardiographic changes in Rett syndrome
Electrocardiographic findings in Rett syndrome
Electrocardiographic findings in Rett syndrome: an explanation for sudden death?
Electrocortical arousal and spindles on physiological cortico-subcortical interactions
Electroencephalogram abnormalities in children with autism spectrum disorders
Electroencephalogram in developmental delay: specific electroclinical syndromes
Electroencephalographic abnormalities in Rett syndrome
Electroencephalographic abnormalities in Rett's syndrome
Electroencephalographic findings in Rett syndrome
Electroencephalographical study of the Rett syndrome with special reference to the monorhythmic theta activities in adult patients
Electromagnetic stimulation of motor neurons
Electron-dense lipidic capillary deposits in Rett syndrome
Elevated CSF beta-endorphin immunoreactivity in Rett's syndrome: report of 158 cases and comparison with leukemic children
Elevated CSF glutamate in Rett syndrome
Elevated CSF lactate in the Rett syndrome: cause or consequence?
Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation
Emotional and behavioural aspects of Rett syndrome
Emotional facial paralysis in Rett syndrome?
Emotional facial paralysis in the Rett syndrome
Endocrinological study on growth retardation in Rett syndrome
Endogenous opioids: their role in autism and Rett syndrome
Enhancing communication skills of girls with Rett syndrome through music therapy
Epidemiology and the geographical distribution of Rett syndrome in Albania
Epidemiology of Rett syndrome
Epidemiology of Rett syndrome in the Spanish population
Epidemiology of Rett syndrome: a community-based study in Tama, Tokyo [Translation]
Epidemiology of Rett syndrome: a population-based registry
Epidural analgesia for pain relief after scoliosis surgery in a patient with Rett's syndrome
Epigenetic consequences of nucleosome dynamics
Epigenetic deregulation of genomic imprinting in human disorders and following assisted reproduction
Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.
Epigenetic study of Rett's syndrome as an adequate model for autistic disorders [Translation]
Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparing
Epilepsy and Rett syndrome - A practical guide for parents
Epilepsy in a population of mentally retarded children and adults
Epilepsy in a representative series of Rett syndrome
Epilepsy in Rett syndrome
Epilepsy in Rett syndrome - A brief overview
Epilepsy in Rett syndrome [Translation]
Epilepsy in the Rett syndrome
Epileptiform abnormalities during sleep in Rett syndrome
Erratum: A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome
Erythrocyte enzymes and substrates in children with Down's syndrome [Translation]
Establishment of platelet-mediated transmitochondrial cell model [Translation]
Evaluation of activities and function in paralytic scoliosis and the diagnosis of Rett's syndrome
Evaluation of two X chromosomal candidate genes for Rett syndrome: glutamate dehydrogenase-2 (GLUD2) and rab GDP-dissociation inhibitor (GDI1)
Everyday choices
Evidence of somatic mosaicism for a MECP2 mutation in females with Rett syndrome: diagnostic implications
Evoked potentials in the Rett syndrome
Evoking communication in Rett syndrome: comparisons with conversations and games in mother-infant interaction
Evolution of clinical signs
Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis
Examination technics in metabolic brain damage with special reference to thin-layer chromatography [Translation]
Exclusion of the gastrin-releasing peptide receptor (GRPR) locus as a candidate gene for Rett syndrome
Experts' meeting on the theme Social aspects of the mental-emotional disability in children [Translation]
Expression of MeCP2 in olfactory receptor neurons is developmentally regulated and occurs before synaptogenesis
Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice
Expression of the methyl-CpG-binding protein MeCP2 in rat brain. An ontogenetic study
Expression pattern of the Rett syndrome gene MeCP2 in primate prefrontal cortex
Extrapyramidal involvement in Rett syndrome
Extrapyramidal involvement in Rett's syndrome
Facilitated communication and Rett syndrome
Facilitating communication in children with multiple disabilities: three case studies of girls with Rett syndrome
Familial aggregation in Rett syndrome: what is the evidence for clustering of other disorders in families of affected girls?
Families' experiences with Rett syndrome - Stress and coping
Families living with Rett syndrome: their needs and social support networks in Australia
Family data in Rett syndrome: association with other genetic disorders
Family social problems in the Rett syndrome
Farewell adress and closing
Features of autism in Rett syndrome and severe mental retardation
Feeding ability in Rett syndrome
Feeding impairments in children: diagnosis and effective intervention
Feeding in Rett syndrome
Feeding of mentally handicapped children [Translation]
Feeding problems in Rett girls [Translation]
Feeding problems in Rett syndrome: Part 2 - Control of respiration
Fetal alcohol syndrome in association with Rett syndrome
Findings from a multidisciplinary clinical case series of females with Rett syndrome
First gene connected to autism spectrum disorders has been found [Translation]
FISH analysis of replication and transcription of chromosome X loci: new approach for genetic analysis of Rett syndrome
Five de novo forms of polymorphisms first found in Chinese mitochondrial genome [Translation]
Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy
Flemish Society of Neurology-Psychiatry-Neurology Section. The role of X chromosome inactivation on the manifestation of Rett Syndrome
Follow-up of monozygotic twins concordant for the Rett syndrome
Forensic problems in Rett syndrome
Four adult Rett patients at an institution for the handicapped
Fra(X)(p22) not associated with infantile autism
Fragile X and Rett syndromes in Puerto Rico
French projects
From birth to five years in Rett syndrome - classic cases only
From comparative genomics to ‘molecular bioinformatics’: an integrated approach to functional genomics
From dad's heart
Frontal lobe disinhibition, Rett syndrome and attention deficit hyperactivity disorder
Frontal lobe functions and dysfunctions
Functional analyses of MeCP2 mutations associated with Rett syndrome using transient expression systems
Functional consequences of Rett syndrome mutations on human MeCP2
Functional evidence of brain stem immaturity in Rett syndrome
Functional significance of MeCP2 mutations in patients with Rett syndrome [Translation]
Functional status, medical impairments, and rehabilitation resources in 84 females with Rett syndrome: a snapshot across the world from the parental perspective
Funding the discovery
Further documentation of familial Rett syndrome
Further EEG observations in children with the Rett syndrome
Games and play in the Rett syndrome
Gangliosides and other neuronal cell markers in Rett syndrome: potential role in pathology and diagnoses
Gangliosides for early differential diagnosis between Rett syndrome and infantile neuronal ceroid lipofuscinosis
Gastrointestinal concerns
Gastrointestinal crises in Rett syndrome
Gastrointestinal manifestations of Rett syndrom
Gastro-oesofagal reflux illness in mentally handicapped people in The Netherlands and Belgium [Translation]
Gastrostomies in Rett syndrome - Parents' experiences
Gastrostomy in Rett Syndrome
Gene defect linked to Rett syndrome
Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations
Gene expression profiling in postmortem Rett syndrome brain: differential gene expression and patient classification
Gene for common cause of mental retardation identified
Gene mapping of the Rett syndrome
Gene questions and answers
General and oral characteristics in Rett syndrome
General and oral characteristics in Rett syndrome [Translation]
General neurological problems in Rett syndrome
Generation and characterization of mice lacking gastrin-releasing peptide receptor
Genes for synapsin I, a neuronal phosphoprotein, map to conserved regions of human and murine X chromosomes
Genetic analyses of DNA methyltransferase genes in mouse model system
Genetic and transcription analysis in Rett syndrome
Genetic aspects of Rett syndrome
Genetic background of Rett syndrome
Genetic basis for Rett disease [Translation]
Genetic basis of Rett syndrome
Genetic causes of mental retardation
Genetic considerations and clues from molecular genetics
Genetic counselling and human handicap [Translation]
Genetic effects of methylation diets
Genetic horizons
Genetic hypothesis in Rett syndrome: the French experience
Genetic implications of Rett syndrome
Genetic studies in Rett syndrome
Genetic studies of neurological disorders : Rett syndrome and HD-like familial prion disease
Genetic studies of Rett syndrome, HD-like neurodegenerative disorder and a variant of limb-girdle muscular dystrophy
Genetic study of 20 patients with autism disorders [Translation]
Genetics and Rett syndrome
Genetics for dummies
Genetics of autism
Genetics of autism: from genome scans to candidate genes [Translation]
Genetics of childhood disorders: XIV. A gene for Rett syndrome: news flash
Genetics of Rett syndrome: properties of the newly discovered gene and pathobiology of the disorder
Genetics of Rett syndrome: properties of the newly discovered gene and the pathophysiology of the disorder
Genetics of the Rett syndrome
Genomic imprinting
Genomic structure of a human holocytochrome c-type synthetase gene in Xp22.3 and mutation analysis in patients with Rett syndrome
Genotype and early development in Rett syndrome: the value of international data
Genotype-phenotype correlations in Rett syndrome: the study of Russian cohort of patients [Translation]
Germline mosaicism in Rett syndrome identified by prenatal diagnosis
Giant somatosensory evoked potentials in Rett syndrome [Translation]
Giant somatosensory evoked potentials in the Rett syndrome
Girl interrupted
Girls with a disturbed development through Rett syndrome [Translation]
Girls with Rett's syndrome have abnormal bone status, increased fracture risk
Girls-only disorder a puzzle
Glial fibrillary acidic protein in the cerebrospinal fluid of children with autism and other neuropsychiatric disorders
Global developmental disorders--etiology and classification dilemmas [Translation]
Glycosphingolipids in patients with the Rett syndrome
Godt Nytt Aer (Translation: Happy new year)
Golgi studies of dendritic morphology in the cerebral cortex in Rett syndrome
GP alert on Rett syndrome study
Grief dancers. A journey into the depths of the soul
Grieving, coping & renewing
Gross motor ability in Rett syndrome - the power of expectation, motivation and planning
Gross motor disability and head growth in Rett syndrome - A preliminary report
Gross rearrangements in the MECP2 gene in three patients with rett syndrome: Implications for routine diagnosis of Rett syndrome
Gross rearrangements of the MECP2 gene are found in both classical and atypical Rett syndrome
Growing up with Rett syndrome in the family
Growing up, where to live?
Growth and nutrition in 10 girls with Rett syndrome
Growth and nutrition in Rett syndrome
Growth and nutrition, feeding issues
Growth failure, encephalopathy, and endocrine dysfunctions in two siblings, one with 5-Oxoprolinase deficiency
Growth retardation in Rett syndrome
Guidance for therapists
Guidelines for reporting clinical features in cases with MECP2 mutations
Guidelines for reporting clinical features in cases with MECP2 mutations, by Allison Kerr and an international group
Hair copper and zinc concentrations in the Rett syndrome
Hand and foot growth failure in Rett syndrome
Hand and foot growth failure in Rett syndrome
Hand in hand with Rett syndrome. Proceedings of the world congress on Rett syndrome, Gothenburg, Sweden, August 30-September 1, 1996
Hand in hand with Rett syndrome. Proceedings of the world congress on Rett syndrome, Gothenburg, Sweden, August 30-September 1, 1996 [Translation]
Hand in hand with Rett syndrome. Proceedings of the world congress on Rett syndrome, Gothenburg, Sweden, August 30-September 1, 1996 [Translation]
Hand preference, extent of laterality, and functional hand use in Rett syndrome
Handedness and developmental disorder
Handwringing and gait in Rett syndrome
Handwringing in Rett syndrome: a normal developmental stage
Hannah at the School Media Centre
Having friends and Rett syndrome: how social relationships create meaningful contexts for limited skills
HBOT for developmental disabilities including RS and CP
Head growth in Rett syndrome
Head growth in Rett syndrome
Head or hands - AAC for girls with Rett syndrome
Health service use in Rett syndrome
Healthy deliveries from biopsied human embryos
Helle and Maja - two girls with Rett Syndrome! [Translation]
Help for the disabled child. With an introduction by Andreas Rett [Translation]
Helping the patient who has pervasive developmental disorder
Hepatitis A and B in non-institutionalized mentally retarded patients
Hereditary chromosomal mosaicism and its importance for the affected family [Translation]
Hereditary mosaicism: normal-trisomy D, chromosome fragility and new type of mosaicism with D ringformation in descendents [Translation]
Heterogeneity in residual function of MeCP2 carrying missense mutations in the methyl CpG binding domain
High anti-nerve growth factor autoantibodies levels in blood sera in girls with Rett syndrome
High levels of cerebrospinal fluid glutamate in Rett syndrome
High male:female ratio of germ-line mutations: an alternative explanation for postulated gestational lethality in males in X-linked dominant disorders
High prevalence of Rett syndrome in a small area
Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome
Hippotherapy
Histone modifications in Rett syndrome lymphocytes: a preliminary evaluation
History and Challenge of Rett Syndrome
HLA and trisomy 21
Home improvement team
Home needs of the chronically ill Rett syndrome child
Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples
Hoping for the impossible in Baltimore: Brazilian girls with Rett syndrome may aid research that can't help them
Hospital dentistry for a child with Rett's syndrome
How can the Internet help parents of children with rare neurologic disorders?
How mammalian transcriptional repressors work
How Rett syndrome and other disorders affect grandparents
How the methyl-CpG binding protein-related epigenetic disease turns on the genes that produce its symptoms [Translation]
How to map the Rett gene?
Human genetics in the information age
Hydrotherapy application to a Rett syndrome case
Hydrotherapy for Rett syndrome
Hyperammonaemia and cerebral atrophy in childhood [Translation]
Hyperammonemia impairs NMDA receptor-dependent long-term potentiation in the CA1 of rat hippocampus in vitro
Hyperendorphinism in Rett syndrome: cause or result?
Hyperventilation in the awake state: potentially treatable component of Rett syndrome
Identification and molecular characterization of a small 11q23.3 de novo duplication in a patient with Rett syndrome manifestations
Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: is there a need for routine screening?
Identification of genes abnormally regulated in Rett syndrome brain
Identification of MeCP2 mutations in a series of females with autistic disorder
Identifying potential communicative acts in children with developmental and physical disabilities
Imaging in the Rett syndrome: inquiry into the possibilities of 18 FDG-positron emission tomography in people with the Rett syndrome [Translation]
Immature pattern of brain activity in Rett syndrome
Immaturity of medullary cardiorespiratory neurones leading to inappropriate autonomic reactions as a likely cause of sudden death in Rett's syndrome
Immune system investigations in Rett syndrome
Immunoglobulin reactivity in autism and Rett's syndrome
Implications for treatment
Importance of Rett syndrome in child neurology
Impression of the world congress on Rett syndrome [Translation]
Improving functional skills and physical fitness in children with Rett syndrome
In loving memory of Dr. Andreas Rett - 1924-1997
In search of a genetic basis for the Rett syndrome
In the world of the brain - Rett Syndrom [Translation]
Incidence and etiology of Down's syndrome [Translation]
Increase support to patients with Rett syndrome! [Translation]
Increased body protein degradation is associated with lean body mass deficits in girls with Rett Syndrome
Increased dendritic complexity and axonal length in cultured mouse cortical neurons overexpressing methyl-CpG-binding protein MeCP2
Increased energy expenditure associated with repetitive involuntary movement does not contribute to growth failure in girls with Rett syndrome
Increased urinary neopterin concentrations in the early phase of Rett's syndrome
Indication for genetic testing: A checklist for Rett syndrome
Induced abortion and brain damage [Translation]
Infantile autism and Rett's syndrome: common chromosomal denominator
Infantile cerebral disorders. Clinical-neuropathological correlations to elucidate the aetiological factors
Infantile hypotonia as a presentation of rett syndrome
Influence of eye movements on Rett stereotypies: evidence suggesting a stage-specific regression
Influence of MECP2 gene mutation and X-chromosome inactivation on the Rett syndrome phenotype
Influence of mutation type and location on phenotype in 123 patients with Rett syndrome
Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes
Inherited metabolic diseases: beyond newborn screening
Injury and plasticity in the developing brain
Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation
Insulin-dependent diabetes mellitus presenting with ketoalkalosis in Rett syndrome
Insulin-like growth factor-I in cerebrospinal fluid and serum in Rett syndrome
Intention and preference in a 3-year old girl with Rett syndrome
Intentional communication in girls with Rett Syndrome
Intentionality and communication in four children with Rett syndrome
Intermediate results of music therapy in interdisciplinary work with Rett syndrome in Institut Haus Der Barmherzigkeit, Vienna
International study on Rett syndrome by the parent organisation; method: questionnaire for parents
Interpreting your MecP2 analysis results
InterRett and RettBASE: International Rett Syndrome Association databases for Rett syndrome
InterRett--The application of bioinformatics to International Rett syndrome research
Intrathecal baclofen for spasticity management in Rett syndrome
Introduction
Introduction
Introduction: Rett syndrome
Investigation of the potential relationship between stereotypical behaviour and respiratory dysrhythmia in Rett disorder and research
Investigation of UBE3A and MECP2 in Angelman syndrome (AS) and patients with features of AS
Investigations of erythrocyte metabolism in trisomy 21 [Translation]
Investigations of the genetics and molecular pathology of Rett syndrome
Involvement of the autonomic nervous system in the pathophysiology of Rett syndrome
Irrecoverable Rett girls [Translation]
Irrecoverable Rett girls? Physiotherapy for the Rett syndrome [Translation]
Irregular phenotypic expression of ring chromosomes
Is classical Rett syndrome ever present in males?
Is Rett syndrome a chromosome breakage syndrome?
Is Rett syndrome a loss-of-imprinting disorder?
Is Rett syndrome a mitochondrial disease?
Is Rett syndrome a subplate disease?
Is Rett syndrome a subtype of pervasive developmental disorders?
Is Rett syndrome caused by a triplet repeat expansion?
Is Rett's syndrome a disorder of carbohydrate metabolism? Hyperpyruvicacidemia and treatment by ketogenic diet
Is the early development of girls with Rett disorder really normal?
Is the girl with Rett syndrome normal at birth?
Isolation of a yeast artificial chromosome contig spanning the X chromosomal translocation breakpoint in a patient with Rett syndrome
It's a knockout! Male infertility and neuropathology
Japanese monozygotic twins with Rett syndrome
Ketogenic diet in Rett syndrome
Ketogenic diet in Rett syndrome
Keynote address: all in the family
Keynote address: in the garden
Kids ask about Rett syndrome
Know the facts - share our hope
Lamotrigine in Rett syndrome
Lamotrigine in Rett syndrome
Lamotrigine in Rett syndrome - Preliminary data from a pilot study
Lamotrigine in Rett syndrome: treatment experience from a pilot study
Lamotrigine in two cases of Rett syndrome
Language and behavioral disturbances associated with epileptiform EEGs
Large deletions of the MECP2 gene detected by gene dosage analysis in patients with Rett syndrome
Large genomic rearrangements in MECP2
Laying the groundwork
L-Carnitine as as treatment for Rett syndrome
L-Carnitine: does it offer benefits for females with Rett syndrome?
L-Carnitine: therapeutic applications of a conditionally-essential amino acid
Lean body mass deficit in girls with Rett syndrome is not associated with altered urea production and salvage
Learning ability in children with Rett syndrome
Learning from less common disorders
Learning, memory, and transcription factors
Left-handed people. Analysis of a minority [Translation]
Levels of cerebrospinal fluid nerve-growth factor differ in infantile autism and Rett syndrome
Lily's journey to independent reading
Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28
Linkage analysis of the Rett syndrome using human chromosomal specific probes
Liva has Rett syndrome [Translation]
Localised proton magnetic resonance spectroscopy (MRS) of the brain in Rett syndrome
Longitudinal observation of electroencephalograms in the Rett syndrome
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location
Long-term persistence of intrathecal viral anti-body responses in postinfectious diseases of the central nervous system and in Rett syndrome
Looking from the inside out: a parent's perspective
Looping out links Rett syndrome with loss of imprinting error
Loss of silent chromatin looping and impaired imprinting of DLX5 in Rett syndrome
Lost in translation: Translational interference from a recurrent mutation in exon 1 of MECP2
Low CSF HVA levels in the Rett syndrome: a reflection of restricted synapse formation?
Low levels of nerve growth factor (NGF) in cerebrospinal fluid (CFS) of children with Rett syndrome
Low levels of nerve growth factor in cerebrospinal fluid of children with Rett syndrome
Low plasma carnitine in Rett syndrome
Low-pressure hyperbaric oxygen therapy (HBOT) as an investigational treatment for developmental disabilities including Rett syndrome and cerebral palsy: theoretical rationale, early results, protocol, and risk/benefit analysis
LTG therapy in 5 patients with Rett Syndrome and epilepsy with the onset in the first 24 months of age [Translation]
Lymphoblastoid cell lines of Rett syndrome patients exposed to oxidative-stress-induced apoptosis
Lymphocyte function in autism and Rett syndrome
Macrocephalic mental retardation associated with a novel C-terminal MECP2 frameshift deletion
Magnesium for hyperventilation in Rett's syndrome
Magnetic resonance imaging and clinical findings examined in adulthood-studies on three adults with Rett syndrome
Magnetic resonance imaging and magnetic resonance spectroscopy studies in Rett syndrome.
Magnetic resonance spectroscopy and analysis of MECP2 in Rett syndrome
Maintaining functional hand use and maximizing the potential for communication
Making inclusion work
Making tough decisions and finding appropriate placement
Making use of augmentative and alternative communication
Male Rett syndrome variant: application of diagnostic criteria
Male Rett variant
Mama was right, -a misunderstood syndrome [Translation]
Management of Rett syndrome: A ten year experience
Management of seizure disorders in Rett syndrome
Management of young children with Rett disorder in the controlled multi-sensory (Snoezelen) environment
Managing scoliosis in a young child with Rett syndrome: a case study
Manipulation of neurotransmitters by acupuncture (?) (A preliminary communication)
Me too I can read. A reader for disabled children. With a preface by Andreas Rett [Translation]
Meaning in music: non-verbal communication in music therapy for girls with Rett syndrome
Measuring the impact of a birth defect: a parental perspective
MECP2 analysis in mentally retarded patients: implications for routine DNA diagnostics
MECP2 analysis in possible familial Rett syndrome
MECP2 and beyond: phenotype-genotype correlations in Rett syndrome
MeCP2 and other methyl-CpG binding proteins
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression
MeCP2 expression and function during brain development: implications for Rett syndrome's pathogenesis and clinical evolution
MeCP2 expression in human cerebral cortex and lymphoid cells: immunochemical characterization of a novel higher-molecular-weight form
MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features
MECP2 gene mutation analysis in Chinese patients with Rett syndrome
MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region
MECP2 gene mutations in non-syndromic X-linked mental retardation: phenotype-genotype correlation
MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution
MeCP2 in neurons: closing in on the causes of Rett syndrome
MECP2 is highly mutated in X-linked mental retardation
MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions
MECP2 mutation analysis in patients with mental retardation
MECP2 mutation in a boy with severe neonatal encephalopathy: clinical, neuropathological and molecular findings
MECP2 mutation in male patients with non-specific X-linked mental retardation
MECP2 mutation in non-fatal, non-progressive encephalopathy in a male
MECP2 mutation screening in Swedish classical Rett syndrome females
MECP2 mutations account for most cases of typical forms of Rett syndrome
MeCP2 mutations found in Rett patients
MeCP2 mutations in children with and without the phenotype of Rett syndrome
MECP2 mutations in Danish patients with Rett syndrome: High frequency of mutations but no consistent correlations with clinical severity or with the X chromosome inactivation pattern
MECP2 mutations in Israel: implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndrome
MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain
MECP2 mutations in Rett syndrome: genotype and phenotype evaluation of 63 patients
Mecp2 mutations in sporadic cases of rett syndrome are almost exclusively of paternal origin
MECP2 mutations in Swedish Rett syndrome clusters
MECP2 mutations or polymorphisms in mentally retarded boys : diagnostic implications
MECP2 structural and 3'-UTR variants in schizophrenia, autism and other psychiatric diseases: a possible association with autism
MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome
MECP2 truncating mutations cause histone H4 hyperacetylation in Rett syndrome
MeCP2: the chromatin connection and beyond
Medical / research updates
Medical and general management of Rett syndrome girls
Medical Q & A panel
Medical updates with questions and answers
Medium-term open label trial of L-carnitine in Rett syndrome
Meeting report: second international Rett syndrome workshop and symposium
Melatonin and the Rett syndrome disorder
Melatonin treatment of Rett syndrome-associated sleep disorders
Membrane cerebral lipids in Rett syndrome
Mental retardation
Mental retardation in children. Prevalence and etiology [Translation]
Mental retardation, "coarse" face, and hyperbreathing: confirmation of the Pitt-Hopkins syndrome
Metabolic and molecular genetic studies on familial cases of Rett syndrome
Metabolic investigation of a patient with Rett syndrome
Metacarpophalangeal pattern profile and bone age in Rett syndrome: further radiological clues to the diagnosis
Method for detecting Rett symdrome and detection kit
Methyl CpG binding proteins: coupling chromatin architecture to gene regulation
Methylated cytosine and the brain. a new base for neuroscience
Methylation gets SMRT. Functional insights into Rett syndrome
Methylation moves into medicine
Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms
Methyl-CpG binding proteins in the nervous system
Methyl-CpG-binding protein 2 is localized in the postsynaptic compartment: an immunochemical study of subcellular fractions
Methyl-CpG-binding protein 2 mutations in Rett syndrome
Methylmercury exposure in Rett syndrome
Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3
Microcephaly: general considerations and aids to nosology
Microscopic observations of the brain in Rett syndrome
Middle and short latency somatosensory evoked potentials(SEPm, SEPs) in the Rett syndrome: chronological changes of cortical and subcortical involvements.
Mild overexpression of MeCP2 causes a progressive neurological disorder in mice
Mind and brain in Rett disorder
Minor form of trigonocephaly is an autistic skull shape? A suggestion based on homeobox gene variants and MECP2 mutations
Mirror writing ability is genetic and probably transmitted as a sex-linked dominant trait: it is hypothesised that mirror writers have bilateral language centres with a callosal interconnection
Mitochondrial alterations in Rett syndrome
Mitochondrial diseases and myopathies: a series of muscle biopsy specimens with ultrastructural changes in the mitochondria
Mitochondrial disturbancies in children with Rett syndrome
Mitochondrial DNA studies in Rett's syndrome
Mitochondrial dysfunction in Rett syndrome. An ultrastructural and biochemical study
Modeling classic female Rett syndrome in male mice
Modelling brain diseases in mice: the challenges of design and analysis
Modifying adult interactions style as positive behavioural intervention for a child with Rett syndrome
Molecular analysis of Japanese patients with Rett syndrome: Identification of five novel mutations and genotype-phenotype correlation
Molecular analysis of synapsin I, a candidate gene for Rett syndrome
Molecular analysis of the Rett syndrome using cDNA synapsin I as a probe
Molecular and cytogenetic analyses on Brazilian youths with pervasive developmental disorders
Molecular and neurobiology aspects of Rett syndrome
Molecular approaches to the Rett syndrome gene
Molecular biological studies about the genetics of Rett syndrome and febrile convulsion in child neurology in China
Molecular biology. MeCP2 repression goes nonglobal
Molecular characterization and genotype-phenotype correlation Italian patients with Rett syndrome
Molecular cytogenetic studies of chromosomal abnormalities and disorders in nervous and mental diseases: search for biological markers for diagnosis [Translation]
Molecular diagnostic of Rett syndrome
Molecular evolution of the synapsin gene family
Molecular genetic studies in familial Rett syndrome
Molecular genetics and neurobiology of neurodegenerative and neurodevelopmental disorders
Molecular genetics of human cognition
Molecular genetics of Rett syndrome
Molecular genetics of Rett syndrome
Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations
Molecular-cytogenetic and cytogenetic investigations of Rett syndrome in children
Molecular-cytogenetic approaches for preclinical diagnosis of Rett syndrome
Molecular-cytogenetic investigation of skewed chromosome X inactivation in Rett syndrome
Mongolism: biological, pedagogical and social aspects [Translation]
Monogenic causes of X-linked mental retardation
Monosomy 18q syndrome and atypical Rett syndrome in a girl with an interstitial deletion (18)(q21.1q22.3)
Morphologic studies of selective developmental arrest in Rett syndrome
Morphological studies of neocortical areas and basal ganglia in Rett syndrome
Morphological study of neocortical areas in Rett syndrome
Morphological study of the entorhinal cortex, hippocampal formation, and basal ganglia in Rett syndrome patients
Mother and daughter with Rett syndrome
Motion analysis of stereotyped hand movements in Rett syndrome
Motivational conflicts in Rett syndrome
Motor disabilities in the Rett syndrome and physical therapy strategies
Motor function and physiotherapy in Rett Syndrome. A literature study [Translation]
Motor symptoms of the Rett syndrome: abnormal muscle tone, posture, locomotion and stereotyped movement
Mouse models: unravelling Rett
Movement disorders in Rett syndrome [Translation]
MRI and MRS findings in a patient with infantile neuronal ceroid lipofuscinosis
Multicolor fluorescent in situ hybridization on post-mortem brain in schizophrenia as an approach for identification of low-level chromosomal aneuploidy in neuropsychiatric diseases
Multi-institutional survey of the Rett syndrome in Japan
Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders
Multiplex ligation-dependent probe amplification (MLPA) detects large deletions in the MECP2 gene of Swedish Rett syndrome patients
Muscle and fibroblast mitochondrial studies in Rett syndrome
Music and Rett syndrome: a music therapeutic interpretation [Translation]
Music and rhythmic stimuli in the rehabilitation of gait disorders
Music and the Rett disorder: The Swedish Rett Center Survey
Music therapy
Music therapy
Music therapy and Rett syndrome [Translation]
Music therapy and the child with Rett syndrome
Music therapy and the Rett syndrome girl - How can it help?
Music therapy as a tool for assessing hand use and communicativeness in children with Rett syndrome
Music therapy as educational method with point of departure from a pupil with Rett syndrome [Translation]
Music therapy for a girl with Rett's syndrome: balancing structure and freedom
Music therapy for children with Rett syndrome
Music therapy for children with Rett syndrome
Music therapy for children with Rett’s syndrome
Music therapy goals for the Rett syndrome girl
Music therapy in the care of the pre-adolescent girl with Rett syndrome
Music therapy in the Rett syndrom [Translation]
Music therapy in the treatment of Rett syndrome
Music therapy in the treatment of the Rett syndrome
Music therapy of a girl with Rett syndrome and the "bridge" towards the pedagogical daily life [Translation]
Music therapy: a therapeutic intervention for girls with Rett syndrome
Musical responsiveness in the Rett disorder
Mutation analysis in Rett syndrome
Mutation analysis in the MECP2 gene and genetic counselling for Rett syndrome
Mutation analysis of 16S rRNA in patients with Rett syndrome
Mutation analysis of MECP2 and clinical characterization in Korean patients with Rett syndrome
Mutation analysis of MECP2 and determination of the X-inactivation pattern in Hungarian Rett syndrome patients
Mutation analysis of MECP2 gene in patients with Rett syndrome from Czech and Slovak Republics
Mutation analysis of methyl-CpG binding protein family genes in autistic patients
Mutation analysis of mitochondrial DNA of children with Rett syndrome
Mutation analysis of mitochondrial DNA of children with Rett syndrome [Translation]
Mutation analysis of mitochondrial DNAs of 15 children with Rett syndrome and 14 of their mothers
Mutation analysis of mitochondrial transfer RNA genes in Rett syndrome
Mutation analysis of the coding sequence of the MECP2 gene in infantile autism
Mutation analysis of the HDAC 1, 2, 8 and CDKL5 genes in Rett syndrome patients without mutations in MECP2
Mutation analysis of the M6b gene in patients with Rett syndrome
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females
Mutation analysis of the MECP2 gene in patients with Rett syndrome
Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome
Mutation analysis of the methyl-CpG-binding protein 2 gene (MECP2) in Rett patients with preserved speech
Mutation in a boy with language disorder and schizophrenia
Mutation screening in Rett syndrome patients
Mutation screening of candidate genes in Rett syndrome
Mutation spectrum and genotype-phenotype correlation of MECP2 in patients with Rett syndrome [Translation]
Mutation spectrum in patients with Rett syndrome in the German population: Evidence of hot spot regions
Mutational analysis of MECP2 gene in Rett syndrome [Translation]
Mutational analysis of MECP2 in classic Rett syndrome: an update and analysis of expression of truncating alleles
Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome
Mutational analysis of mitochondrial DNA of children with Rett syndrome
Mutational analysis of the MECP2 gene by direct sequencing in Hungarian patients with Rett syndrome [Translation]
Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome
Mutations and polymorphisms in the human methyl CpG-binding protein MECP2
Mutations found within exon 1 of MECP2 in Danish patients with Rett syndrome
Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome
Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in males
Mutations in Italian patients with Rett syndrome
Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome
Mutations in the MECP2 gene in a cohort of girls with Rett syndrome
Mutations in the MeCP2 gene in the Rett syndrome [Translation]
Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardation
Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation
Mutations of the MECP2 gene in Rett syndrome
My eyes can choose [Translation]
My girl is different, chapter "Lotta" [Translation]
My sister and me
Naloxone in ameliorating hyperventilation-apnea attacks in the Rett syndrome
Naltrexone in the management of seizures associated with Rett syndrome
Natural history, search for a marker and therapy
Neither uniparental disomy nor skewed X-inactivation explains Rett syndrome
Neonatal 192 IgG-saporin lesion of forebrain cholinergic neurons: focus on the life span?
Neonatal cholinergic and catecholaminergic lesions as a model for disorders of forebrain neuronal dysgenesis
Neonatal citrullinemia: comparison of conventional MR, diffusion-weighted, and diffusion tensor findings
Neonatal convulsions against the background of an epileptically laden family [Translation]
Neonatal encephalopathy in two boys in families with recurrent Rett syndrome
Nerve growth factor plasma levels and ventricular epolarization in Rett syndrome
Neues aus dem Rettland (Translation: News from Rettland)
Neural and behavioral effects of intracranial 192 IgG-saporin in neonatal rats: sexually dimorphic effects?
Neuro MR imaging: a window into structure and function
Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossa
Neuroanatomy of Rett syndrome: a volumetric imaging study
Neurobiology and neurochemistry of Rett syndrome
Neurobiology and neurochemistry of Rett syndrome
Neurobiology of Rett syndrome
Neurobiology of Rett syndrome
Neurobiology of Rett syndrome: a genetic disorder of synapse development
Neurochemical alterations in Rett syndrome
Neurochemical aspects of the Rett syndrome
Neurochemistry of the Rett syndrome
Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2)
Neurogenic spinal deformities. I. Conservative and surgical treatment of spinal deformities [Translation]
Neuroimage in infants and children with mitochondrial disorders
Neuroimaging and neurochemical studies of Rett syndrome [Translation]
Neuroimaging of developmental and genetic disorders
Neuroimaging studies in Rett syndrome
Neurological manifestation and genetic diagnosis of Angelman, Rett and Fragile-X syndromes [Translation]
Neurometabolism in Rett syndrome
Neuronal abnormalities in Rett syndrome: studies by nasal biopsy
Neuronal ceroid-lipofuscinoses – Demential diseases in childhood and adolescence
Neuronal instability: implications for Rett's syndrome
Neurons and neuronal systems involved in the pathophysiologies of Rett syndrome
Neuropathological studies in a child showing some features of the Rett syndrome
Neuropathology and immunohistochemistry of brains with Rett syndrome [Translation]
Neuropathology and neurochemistry
Neuropathology of Rett syndrome
Neuropathology of Rett syndrome
Neuropathology of Rett syndrome
Neuropathology of Rett syndrome: case report with neuronal and mitochondrial abnormalities in the brain
Neurophysiological diagnosis
Neurophysiological findings in the Rett syndrome
Neurophysiological findings in the Rett syndrome, 1: EMG, conduction velocity, EEG and somatosensory-evoked potential studies
Neurophysiological findings in the Rett syndrome, 2: Visual and auditory brainstem, middle and late evoked responses
Neurophysiological observations in corticospinal projections to the upper limb in subjects with Rett syndrome
Neurophysiology of Rett syndrome
Neurophysiology of Rett syndrome
Neurotransmitter alterations in Rett syndrome brain
Neurotrophic factors in cerebrospinal fluid and serum of patients with Rett syndrome
Neurotrophic factors in the pathogenesis of Rett syndrome
Neurotrophic factors in the pathogenesis of Rett syndrome
New experience with Rett syndrome in France: the problem of atypical cases
Newsletter
Newsletter
Newsletter
Newsletter
Nieuwsbrief Rett Syndroom Netwerk (Translation: Newsletter Rett Syndrome Network)
No correlation between phenotype and genotype in boys with a truncating MECP2 mutation
No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patients
Non-invasive behavioral treatment of self-injurious hand stereotypy in a child with Rett syndrome
Non-random X chromosome inactivation in patients with Rett syndrome and in their mothers
Normal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteins
Normal latencies of cortical somatosensory evoked potentials--an additional criterion for the diagnosis of Rett syndrome [Translation]
Norwegian video on the Rett syndrome [Translation]
Not without language. Facilitated Communication for a Rett girl [Translation]
Note on Rett syndrome symposium
Nothing can be done for our baby
Notiziario (Translation: News bulletin)
Novel de novo nonsense mutation of MECP2 in a patient with Rett syndrome
Novel mitochondrial 16S rRNA polymorphism in a girl with Rett syndrome
Nurse recognition of early deviation in development in home videos of infants with Rett disorder
Nutrition and weight
Nutrition care guidelines for Rett syndrome
Nutrition in Rett syndrome
Nutrition in Rett Syndrome
Nutritional and auxologic patterns in Italian patients with Rett syndrome
Nutritional aspects of Rett syndrome
Nutritional disorders in Rett syndrome
Nutritional needs of children with Rett syndrome
Nutritional treatments for Rett's, autism
Observation of the Rett syndrome with particular attention to the body perception [Translation]
Observations on hand movements in Rett syndrome: a pilot study
Occupational therapy
Occurrence of Rett syndrome in boys
Occurrence of Rett syndrome in males
Ocular signs in cases of down's syndrome [Translation]
Odd MECP2-mutated Rett variant-long-term follow-up profile to age 25
Olfactory biopsies demonstrate a defect in neuronal development in Rett's syndrome
Olfactory receptor neuronal abnormalities in Rett syndrome
On a unusual brain atrophy syndrome in hyperammonemia in childhood [Translation]
On an until now unknown disease of a congenital metabolic disorder [Translation]
On clinical and therapeutic problems of spike-wave complexes and their variants in EEG of children [Translation]
On differential diagnostics in neonatal autism: according to the Rett syndrome model [Translation]
On Rett's syndrome. Regional children's clinical hospital: clinico-diagnostic and organizational problems [Translation]
On the diagnosis and therapy of metabolic brain damage in childhood [Translation]
On the genetics of Rett syndrome: analysis of family and pedigree data
On the genetics of the Rett syndrome
On the prevalence of Rett syndrome in Switzerland [Translation]
On the problem of sensitivity to pain in childhood [Translation]
On the therapy of centrocephalic epilepsy in childhood [Translation]
On the use of vitamin B 12 in children with brain damage Comparative studies of the serum level in caynacobalamin and hydroxycobalamin [Translation]
On the usefulness of syndrome analysis according tot the model of the Rett syndrome [Translation]
One child out of a thousand is affected by autism. Sweden has leading position in pediatric neurology/psychiatry [Translation]
One family’s success with facilitated communication
Operant studies of self-injurious hand biting in the Rett syndrome
Ophthalmological symptoms of infantile cerebral palsy [Translation]
Optimizing epilepsy therapy in children and adolescents with lamotrigine [Translation]
Oral health in children with Rett syndrome [Translation]
Oral manifestation of Rett's syndrome
Oral manifestations in Rett syndrome: a study of 17 cases
Oral manifestations in Rett syndrome: clinical and therapeutic aspects [Translation]
Oral motor dysfunction and feeding problems in Rett syndrome
Organ growth in Rett syndrome
Organ growth in Rett syndrome: a postmortem examination analysis
Orientation in space
Origin of the extra chromosome no 21 in Down's syndrome
Oropharyngeal dysfunction and gastroesophageal dysmotility are present in girls and women with Rett syndrome
Oropharyngeal dysfunction and upper gastrointestinal dysmotility
Orthopaedic aspects of Rett syndrome: a multicentre review
Orthopaedic aspects of Rett's syndrome: brief report
Orthopaedic management of Rett syndrome
Orthopaedic manifestations of Rett syndrome
Orthopaedic update in Rett syndrome
Orthopaedics
Orthopaedics
Orthopedic aspects of Rett syndrome [Translation]
Orthopedic aspects of Rett's syndrome [Translation]
Orthopedic problems in patients with Rett syndrome
Orthopedic problems in Rett syndrome
Orthopedic problems in the Rett syndrome [Translation]
Orthopedics and Rett syndrome [Translation]
Osteopenia in Rett syndrome
Otoacoustic emission findings in Rett syndrome
Outcome in Rett syndrome. Outcomes in neuro-developmental and genetic disorders
Outcomes of genetic evaluation in children with pervasive developmental disorder
Oxidative metabolism in Rett syndrome: 1. Clinical studies
Oxidative metabolism in Rett syndrome: 2. Biochemical and molecular studies
Oxidative stress in Rett syndrome
p.R270X MECP2 mutation and mortality in Rett syndrome
Paediatric nursing and education students' attitudes toward children with Rett syndrome: a pilot study
Paradoxical role of methyl-CpG-binding protein 2 in Rett syndrome
Parent idea book 'Managing Rett syndrome'
Parent survival manual - A guide to crisis resolution in autism and related developmental disorders
Parental origin of de novo MECP2 mutations in Rett syndrome
Parental origin of the X chromosome in Rett’s syndrome
Parental origin of the X chromosomes in Rett Syndrome
Parents' evidence for the education and therapeutic interventions [Translation]
Parents helping parents - Making a difference
Partial monosomy and trisomy 5 p due to balanced translocation t (3,5) in the father [Translation]
Partial trisomy 4q in two unrelated cases
Pathobiochemical aspects of cytoskeleton components
Pathological changes in substantia nigra and basal forebrain cholinergic neurons in Rett syndrome
Pathophysiology of Rett syndrome
Pathophysiology of Rett syndrome from the stand point of clinical characteristics
Pathophysiology of Rett syndrome from the standpoint of early catecholamine disturbance
Pathophysiology of Rett syndrome from the standpoints of clinical characteristics and clinical neurophysiological findings [Translation]
Pathways to learning in Rett syndrome
Patients with the R133C mutation: is their phenotype different from patients with Rett syndrome with other mutations?
Pattern of brain and organ growth in Rett's syndrome supports hypothesis of cerebral developmental arrest
Patterns of mortality and long-term prognosis in Rett syndrome
Patterns of pregnancy loss, perinatal mortality, and postneonatal childhood deaths in families of girls with Rett syndrome
Patterns of X chromosome inactivation in the Rett syndrome
Pedigree analysis of Hungarian Rett syndrome girls
Pedopsychiatric topics of Rett syndrome and its relation with autism [Translation]
Perinatal and infant deaths in families of girls with Rett syndrome
Peripheral lymphocyte subsets and other immune aspects in Rett syndrome
Peripheral nerve findings in Rett syndrome
Peripheral nerve involvement in the Rett syndrome
Personal Communication
Perturbations in the development of infants with Rett disorder and the implications for early diagnosis
Pervasive developmental disorders
Pervasive developmental disorders: controversies concerning the classification of autism [Translation]
Pervasive disintegrative disorder: are Rett syndrome and Heller Dementia Infantilis subtypes?
Pervasive disintegrative disorder?
Pervasive neuroanatomic abnormalities of the brain in three cases of Rett's syndrome
Pharmacological treatment of Rett syndrome - Does it help?
Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome
Physical characteristics of individuals with Rett syndrome: Findings from a multidisciplinary clinical assessment of a case series of 87 girls and adults
Physical growth and development in patients with Rett syndrome
Physical therapy
Physical therapy
Physical therapy
Physical therapy approach to management of scoliosis
Physical therapy strategies
Physiotherapeutic treatment of girls with Rett syndrome [Translation]
Physiotherapeutic treatment of girls with the Rett syndrome, with special reference to children and teenagers [Translation]
Physiotherapy and Rett syndrome
Plasma endorphins in Rett syndrome: preliminary data
Play in brain-damaged children [Translation]
Play in cerebral palsy children [Translation]
Polysomnographic characteristics of patients with Rett syndrome
Polysomnographic recordings of respiratory disturbances in Rett syndrome
Polysomnography in the Rett syndrome
Pons tumour behind a phenotypic Rett syndrome presentation
Population study extends profile of Rett syndrome
Population-based registries using multidisciplinary reporters: a method for the study of pediatric neurologic disorders
Positive aspects / specific problems in the child affected by the Rett syndrome [Translation]
Positron emission tomographic study of D2 dopamine receptor binding and CSF biogenic amine metabolites in Rett syndrome
Positron emission tomography in the Rett syndrome: clinical, biochemical and pathological correlates
Positron emission tomography studies of the dopamine system in Rett syndrome
Possibilities and limits of clonazepam therapy in childhood [Translation]
Possibilities and limits of physiotherapy for children with cerebral paralysis [Translation]
Possibilities of pharmacological treatment of Rett's syndrome
Possible hyperendorphinergic pathophysiology of the Rett syndrome
Possible lesions of the Rett syndrome: opinions of contributors
Possible link between skeletal and electrocardiographic abnormalities and autonomic dysfunction in Rett syndrome
Possible mechanisms of osteopenia in Rett syndrome: bone histomorphometric studies
Postnatal loss of methyl-CpG binding protein 2 in the forebrain is sufficient to mediate behavioral aspects of Rett syndrome in mice
Postnatal neurodevelopmental disorders: meeting at the synapse?
Practical advice: constipation / how to increase the liquid by your child, medicines [Translation]
Practical and theoretical considerations concerning the genetics of Rett syndrome
Practice parameter: evaluation of the child with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and The Practice Committee of the Child Neurology Society.
Predictive value of the early clinical signs in Rett disorder
Pregnancy interruption from the pediatric viewpoint [Translation]
Preliminary analysis of the hereditary model and mitochondrial DNA in the Rett syndrome
Preliminary assessment of choice making among children with Rett syndrome
Preliminary brain autopsy findings in progredient Rett syndrome
Preliminary evidence for neurodegenerative changes in the substantia nigra in Rett syndrome.
Preliminary study of communication and auditive perception in sisters with Rett syndrome [Translation]
Premature birth and brain damage. Symposium of the Austrian Association of Pedatrics [Translation]
Prenatal diagnosis in Rett syndrome
Preserved speech variant is allelic of classic Rett syndrome
Preserved speech variants of the Rett syndrome: molecular and clinical analysis
Prevalence of Fra(X) and other specific diagnoses in autistic individuals in a Danish county
Prevalence of hearing loss in Rett syndrome
Prevalence of pervasive developmental disorders in the British nationwide survey of child mental health
Prevalence of pervasive developmental disorders in the British nationwide survey of child mental health
Prevalence of Rett Syndrome in Italy
Prevalence of Rett syndrome in Switzerland
Prevalence of Rett syndrome in Tokyo [Translation]
Prevalence study of Rett syndrome in North Dakota children
Primary versus secondary stereotypic movements [Translation]
Problems of male dysgenetic pseudohermaphroditism [Translation]
Proceedings of the international meeting on the Rett syndrome. Siena (Italy), April 5-6 1991 [Translation]
Proceedings of the World Congress on Rett Syndrome 2000: Clinico-molecular biological correlation. Karuizawa, Japan. July 24-27, 2000
Professor Vanja Holm's meeting with Victorian parents
Profiling methyl-CpG specific determinants on transcriptionally silent chromatin
Program for training of children with Rett's syndrome
Progress aimed at wholeness and interaction in a female pupil with Rett syndrome, with the phrasing of likely embedding in the learning group education of… [Translation]
Progress in pupils with mental disability - The Rett syndrome [Translation]
Progress in study of genetically determined syndromes and diseases accompanied with disorders of neuro-psychic development in children
Progress in the neurobiology of autism
Progression of CT scan findings in Rett syndrome [Translation]
Progressive cardiac dysautonomia observed in patients affected by classic Rett syndrome and not in the preserved speech variant
Prolonged QT interval in Rett syndrome
Proposal for exercises - Mother/child-play for girls with Rett syndrome [Translation]
Proton magnetic resonance spectroscopy of the brain in three cases of Rett syndrome: comparison with autism and normal controls
Proton MR spectroscopy in Rett syndrome
Psychosocial and family functioning of parents and siblings of children with Rett syndrome
Psycho-syndrome based on organic brain damage in children [Translation]
Pterins in patients with Rett syndrome
Purine and pyridine nucleotide metabolism in the erythrocytes of patients with Rett syndrome
Quantitative 1H MR spectroscopic imaging in early Rett syndrome
Quantitative analysis of immunofluorescence and lipofuscin distribution in human cortical areas by dual-channel confocal laser scanning microscopy
Quantitative analysis of magnetic resonance imaging in Retts syndrome
Quantitative assessment of brain perfusion by ECD-Tc99m SPET in Rett syndrome
Quantitative EEG correlates of the human frontal lobe dysfunction [Translation]
Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry
Quantitative magnetic resonance analysis in Rett syndrome: cerebral and cerebellar abnormalities
Quantitative magnetic resonance imaging and studies of degenerative diseases of the developing human brain
Quantitative magnetic resonance imaging in Rett syndrome
Questions and answers: panel of experts : main topics - Genetics, seizures and medications, breathing, nutrition, therapies
R133C and R168X mutations in Japanese Rett syndrome patients: a caution for misdiagnosis
Racial hygiene. A path in National Socialism [Translation]
Radiological clues to the neuroendocrine basis of Rett syndrome
Range of emotion
Rapid genotyping of common MeCP2 mutations with an electronic DNA microchip using serial differential hybridization
Rare disabilities--less known syndromes. A challenge for neuropsychiatric rehabilitation [Translation]
Real-time quantitative PCR as a routine method for screening large rearrangements in Rett syndrome: Report of one case of MECP2 deletion and one case of MECP2 duplication
Rebecca's gift
Recent developments in neuropathology - Electron microscopy - Brain pathology
Recent developments in Rett syndrome research
Recent experience with Rett syndrome at a tertiary care center
Recent insights into hyperventilation from the study of Rett syndrome
Receptive communication in late-stage Rett syndrome: a cautionary note
Recognition of methylated DNA [Translation]
Recommendations regarding handling of the necropsy in Rett syndrome
Recruiting parents of children with a fatal disease as co-investigators.
Reduced cerebrospinal fluid B-endorphin levels in Rett syndrome
Reduced cholinergic, dopaminergic and glutaminergic biomarkers in Rett syndrome
Reduced concentrations and increased metabolism of biogenic amines in a single case of Rett-syndrome: a postmortem brain study
Reduced concentrations of ascorbic acid and glutathione in a single case of Rett syndrome: a post-mortem brain study
Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett Syndrome
Reduced expression of neuropeptides can be related to respiratory disturbances in Rett syndrome
Reduced folate transport to the brain in Rett syndrome
Reduced folate transport to the CNS in female Rett patients
Reduced heart rate variability in patients affected with Rett syndrome. A possible explanation for sudden death
Reduced nerve growth factor expression in patients with Rett syndrome
Reduced nerve growth factor in Rett syndrome postmortem brain tissue
Reduced proportion of Purkinje cells expressing paternally derived mutant Mecp2308 allele in female mouse cerebellum is not due to a skewed primary pattern of X-chromosome inactivation
Reduction of biogenic amine levels in the Rett syndrome
Refining the phenotype of common mutations in Rett syndrome
Regional cerebral blood flow abnormalities in Rett syndrome
Regional cerebral blood flow in Rett syndrome
Regional cerebral blood flow: SPECT as a tool for localization of brain dysfunction
Regression in individuals with Rett syndrome
Rehabilitation treatment in the Rett syndrome
Relation between time of onset of regression in Rett syndrome and the remaining locomotor behaviour
Reliability and validity of MRI measurement of the amygdala and hippocampus in children with fragile X syndrome
Remarks on the work of A. Rett: "The Thalidomide problem in Austria" (in: Wien. Med. Wschr., 1965, 21) [Translation]
Renovascular hypertension in a child with Rett syndrome
Repetitive motor movements do not increase total daily energy expenditure in Rett's syndrome
Reply to "Should a syndrome be called by its correct name? The example of the preserved speech variant of Rett syndrome" by Zappella et al.
Reply to above letter (i.e. "Parental origin of the X chromosomes in Rett syndrome" by Benedetti L, and others)
Reply to above letter (i.e. "Some remarks regarding the search for a genetic basis for Rett syndrome" by Buhler E.)
Report from the Stockholm meeting 1988 [Translation]
Report from the Vienna meeting 1988 [Translation]
Report of the World Congress in Sweden [Translation]
Report on the Rett syndrome workshop: Glasgow, Scotland, 24-25 May, 1986
Research in Rett syndrome: past, present and future
Research on Rett syndrome: strategy and preliminary results
Research updates
Research updates
Respiration patterns affect feeding in Rett syndrome
Respiration patterns during feeding in Rett syndrome
Respiratory dysrhythmia and engagement of attention in two girls with Rett syndrome
Respiratory pattern of Rett syndrome in overnight sleep
Response: another Rett patient with a typical Angelman EEG
Results of an epidemiological-clinical study of the Rett syndrome in the German Democratic Republic [Translation]
Results of surgery for scoliosis in Rett syndrome
Rethinking the fate of males with mutations in the gene that causes Rett syndrome
Retrospective diagnosis of Rett syndrome variants with photographs in childhood
Rett and Angelman's syndromes: models of arrested development
Rett and ICF syndromes: methylation moves into medicine
Rett Center update: Baylor College of Medicine
Rett Center update: Kennedy Krieger Research Institute
Rett Disorder - the developmental perspective
Rett disorder and the developing brain
Rett females: patterns of characteristic side-asymmetric neuroimpairments at long-term follow-up
Rett Gazet
Rett gene regulates gene expression through silencing
Rett genetics
Rett girls with preserved speech
Rett Lett
Rett meets young victims of disease
Rett News
Rett Nyt (Translation: Rett news)
Rett patients with both MECP2 mutation and 15q11-13 rearrangments
Rett phenotype in patient with XXY karyotype: case report [Translation]
Rett phenotype with X/autosome translocation: possible mapping to the short arm of chromosome X
Rett syndrom - Rett Center [Translation]
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett syndrome
Rett Syndrome - 5 cases in Oman
Rett syndrome - a case report
Rett syndrome - A first foundation [Translation]
Rett syndrome - A prevalence study in three Norwegian counties
Rett syndrome - A talk by Dr. Naidu
Rett syndrome - An early catecholamine and indolamine deficient disorder?
Rett Syndrome - an update
Rett syndrome - Clinical and biological aspects: Studies on 130 Swedish Females
Rett syndrome - Clinical and biological aspects: studies on 130 Swedish females
Rett syndrome - Distribution of phenotypes with special attention to the preserved speech variant
Rett syndrome -- familial recurrence
Rett syndrome -- pathogenesis, genetics, and search for a marker
Rett syndrome - Restricted, classic, and broad variants
Rett syndrome - Search for genetic markers
Rett syndrome "Behind their eyes is more than they can show us"
Rett syndrome (review of the literature) [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome [Translation]
Rett syndrome and ageing: a case study
Rett syndrome and associated movement disorders
Rett syndrome and autism
Rett syndrome and autism
Rett syndrome and autism. Comparative evaluation in the infant using family movies [Translation]
Rett syndrome and autism. Early comparative evaluation for signs of autism using family movies [Translation]
Rett syndrome and autism: a comparative study with home movies
Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots
Rett syndrome and beyond: recurrent spontaneous and familial mutations at CpG hotspots in the methyl-CpG binding protein-2 gene
Rett syndrome and delayed recovery from anaesthesia
Rett syndrome and fragile site in Xp22
Rett syndrome and genetic drift
Rett syndrome and Heller dementia
Rett syndrome and MeCP2: linking epigenetics and neuronal function
Rett syndrome and metabolic disorder
Rett syndrome and mitochondrial enzyme deficiencies
Rett syndrome and music therapy
Rett syndrome and profound intellectual disability: cognitive and communicative similarities and differences
Rett syndrome and the 4th metatarsal
Rett syndrome and the adult patient [Translation]
Rett syndrome and the autistic disorders
Rett syndrome and the electroencephalogram
Rett syndrome and the MECP2 gene
Rett syndrome applications in Turkey
Rett syndrome as a hodogenesis disorder [Translation]
Rett syndrome as a minicolumnopathy
Rett syndrome associated with tuberous sclerosis in a male and in a female: evidence for arrested motor and mental development
Rett syndrome at an institution for the developmentally disabled
Rett syndrome bibliography
Rett syndrome bibliography II, 1987
Rett syndrome diagnostic testing by DHPLC and sequence analysis of the MECP2 gene
Rett syndrome from a family perspective: The Swedish Rett Center survey
Rett syndrome from an orthopedagogic point of view [Translation]
Rett syndrome from quintuple and triple deletions within the MECP2 deletion hotspot region
Rett syndrome gene linked to maintenance of mature neurons
Rett syndrome genetic study
Rett syndrome in a 47,XXX patient with a de novo MECP2 mutation
Rett syndrome in a boy with a 47, XXY karyotype
Rett syndrome in a boy with a 47,xxy karyotype confirmed by a rare mutation in the mecp2 gene
Rett syndrome in a pair of full sisters
Rett syndrome in a patient with medium chain Acyl-CoA dehydrogenase deficiency
Rett syndrome in adolescent and adult females:clinical and molecular genetic findings
Rett syndrome in Australia: epidemiological data-distribution of classical and atypical females
Rett syndrome in Bahrain
Rett syndrome in British paediatric surveillance-unit
Rett syndrome in children: problems of differential diagnosis [Translation]
Rett syndrome in China: report of 9 patients
Rett syndrome in Estonia: prevalence of the classical phenotype
Rett syndrome in females with CTS hot spot deletions: A disorder profile
Rett syndrome in males
Rett syndrome in Mexican children: study of 14 cases
Rett syndrome in monozygotic twins
Rett syndrome in Northern Tuscany (Italy): family tree studies
Rett syndrome in Saudi Arabia: report of six patients
Rett syndrome in South Africa
Rett syndrome in Spain: mutation analysis and clinical correlations
Rett syndrome in Sri Lanka
Rett syndrome in Sweden
Rett syndrome in Sweden
Rett syndrome in Sweden. Neurodevelopment--disability--pathophysiology
Rett syndrome in Thai female girls: clinical studies
Rett syndrome in the developing world
Rett syndrome in the western part of Sweden - care and social problems [Translation]
Rett syndrome in Tunisia
Rett syndrome in Yugoslavia
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
Rett syndrome management with Snoezelen or controlled multi-sensory stimulation. A review.
Rett syndrome model suggests MECP2 gives neurons the quiet they need to think
Rett syndrome neuropathology review 2000
Rett syndrome phenotype following infantile acute encephalopathy
Rett syndrome revisited: a patient with biotin dependency
Rett syndrome studies of natural history and search for a genetic marker
Rett syndrome symptomatology of institutionalised adults with mental retardation: comparison of males and females
Rett syndrome traced to defective gene "silencer"
Rett syndrome update
Rett syndrome variants: an overview
Rett syndrome with preserved speech: social and communication aspects
Rett syndrome, a developmental disorder. Presentation of a variant with preserved speech [Translation]
Rett syndrome, a gene at last!
Rett syndrome, a genetic disease [Translation]
Rett syndrome, classical and atypical: genealogical support for common origin
Rett syndrome, communication for all seasons
Rett syndrome, EEG and the motor cortex as a model for better understanding of attention deficit hyperactivity disorder (ADHD)
Rett syndrome, EEG and the sensorimotor cortex
Rett Syndrome, one-sided sympathectomy - Unilateral foot normalisation
Rett syndrome, rare diseases and UK research
Rett syndrome. A common cause of psychomotor retardation among girls [Translation]
Rett syndrome. A commonly overlooked progressive encephalopathy in girls
Rett syndrome. A frequent cause of progressive mental retardation in girls [Translation]
Rett syndrome. A practical guide for parents, carers and therapists
Rett syndrome. A report of fifteen cases [Translation]
Rett syndrome. A study of 20 cases [Translation]
Rett syndrome. A well defined but mysterious encephalopathy [Translation]
Rett syndrome. An orientation. [Translation]
Rett syndrome. An update and review for the primary paediatrician
Rett syndrome. Developing an educational arrangment based on playing together and sound [Translation]
Rett syndrome. Discovery of the MECP2 gen as genetic marker [Translation]
Rett syndrome. Discovery of the MECP2 gene as genetic marker
Rett syndrome. Evidence for a behavioural phenotype
Rett syndrome. History and general overview
Rett syndrome. Progressive, affects only girls. Rett treatment holds promise
Rett syndrome. Prospectives and instruments of intervention [Translation]
Rett syndrome. Review of the literature and presentation of 2 clinical cases [Translation]
Rett syndrome. The Puerto Rican experience
Rett syndrome: "We'll keep the genes on for you"
Rett syndrome: 1H spectroscopic imaging at 4.1 tesla
Rett syndrome: 1H spectroscopic imaging at 4.1 Tesla
Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents
Rett syndrome: a "new" and rare disease. A clinical case [Translation]
Rett syndrome: a case presenting with atypical seizures. Neurophysiological and clinical aspects
Rett syndrome: a case report
Rett syndrome: a case report from an audiovisual program
Rett syndrome: a case with eye closure absences
Rett syndrome: a case with respiratory impairment
Rett syndrome: a challenge for music therapists
Rett syndrome: a closer look
Rett syndrome: a comprehensive review of the literature
Rett syndrome: a conversation with families
Rett syndrome: a description and analysis of ambulation interventions
Rett syndrome: a disorder affecting early brain growth
Rett syndrome: a disorder caused by a genetic defect [Translation]
Rett syndrome: a genetic disorder in females?
Rett syndrome: a literature review and survey of parents and therapists
Rett syndrome: a longitudinal developmental case report
Rett syndrome: a medical guide for parent-advocates
Rett syndrome: a medical odyssey
Rett syndrome: a mitochondrial disease?
Rett syndrome: a new challenge to the understanding of developmental disabilities
Rett syndrome: a pervasive disorder of growth?
Rett syndrome: a physician's approach
Rett syndrome: a progressive neurological syndrome in girls [Translation]
Rett syndrome: a prototype of motor/mental immaturity or developmental retardation?
Rett syndrome: a prototypical neurodevelopmental disorder
Rett syndrome: a resource and information file
Rett syndrome: a retrospective pilot study on potential early predictive symptomatology
Rett syndrome: a review of current knowledge
Rett syndrome: a review of current knowledge [Translation]
Rett syndrome: a search for etiopathogenetic factors
Rett syndrome: a search for gene sources
Rett syndrome: a significant proportion of girls affected by autistic behaviour
Rett syndrome: a study
Rett syndrome: a study of the face
Rett syndrome: a suggested staging system for describing impairment profile with increasing age towards adolescence
Rett syndrome: a surprising result of mutation in MECP2
Rett syndrome: a survey [Translation]
Rett syndrome: a survey of North American patients
Rett syndrome: a survey on psychological and pedagogical experiences [Translation]
Rett syndrome: a survey on psychological and pedagogical experiences [Translation]
Rett syndrome: a therapeutic approach
Rett syndrome: a useful and simple visual communication aid for daily use
Rett syndrome: a view on care and management
Rett syndrome: abnormal membrane-bound lamellated inclusions in neurons and oligodendroglia
Rett Syndrome: adolescence and adulthood
Rett syndrome: an analysis using Sartwell's incubation period model
Rett syndrome: an EEG study in 52 girls
Rett syndrome: an introduction to Rett syndrome and communication intervention for girls and women who have Rett syndrome
Rett syndrome: an overview from the basic science to the clinical picture
Rett syndrome: an update
Rett syndrome: anaesthesia management
Rett syndrome: anaesthesia management
Rett syndrome: analysis of 4 cases
Rett syndrome: analysis of deaths in the British Survey
Rett syndrome: analysis of electroencephalographic patterns in 27 girls [Translation]
Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients
Rett syndrome: analysis of MECP2 mutations in Brazilian patients
Rett syndrome: aspects of differential diagnostics and therapy
Rett syndrome: associative learning [Translation]
Rett syndrome: biochemical investigations on muscle tissue in a girl with abnormal mitochondria
Rett syndrome: biogenic amines and metabolites in postmortem brain
Rett syndrome: British longitudinal study (1982-1990) and 1990 survey
Rett syndrome: case reports and management strategies
Rett syndrome: case reports and review
Rett syndrome: cerebellar pathology
Rett syndrome: characterisation of seizures versus non-seizures
Rett syndrome: clinical and epidemiological aspects in a Brazilian institution
Rett syndrome: clinical and molecular update
Rett syndrome: clinical and polysomnografic results in two sisters [Translation]
Rett syndrome: clinical aspects and EEG for an early diagnostic assessment [Translation]
Rett syndrome: clinical characteristics and recent genetic advances
Rett syndrome: clinical correlates of the newly discovered gene
Rett syndrome: clinical features, genetic considerations, and the search for a biological marker
Rett syndrome: clinical manifestations in males with MECP2 mutations
Rett syndrome: clinical molecular correlates
Rett syndrome: clinical pecularities and biological mysteries
Rett syndrome: clinical peculiarities, diagnostic approach and possible cause
Rett syndrome: clinical presentation and laboratory investigations in 12 further French patients
Rett syndrome: clinical profile and EEG abnormalities
Rett syndrome: clinical review and genetic update
Rett syndrome: clinical synopsis of 31 cases [Translation]
Rett syndrome: clinical update and review of recent genetic advances
Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28
Rett syndrome: congenital defect of a transcription inhibitory protein [Translation]
Rett syndrome: controlled study of an oral opiate antagonist, naltrexone
Rett syndrome: conversations with Australian families and caregivers
Rett syndrome: correlation of clinical symptoms and the mutations in the gene of methyl CPG binding protein 2 (MeCP2): introductory remarks [Translation]
Rett syndrome: criteria for inclusion and exclusion
Rett syndrome: critical examination of clinical features, serial EEG and video-monitoring in understanding and management
Rett syndrome: current status and new vistas
Rett syndrome: development of a system of classification and gradation in motor behaviour [Translation]
Rett syndrome: diagnosis and treatment [Translation]
Rett syndrome: diagnostic guidelines offered. Syndrome linked to metabolic defect
Rett syndrome: discrimination of typical and variant forms
Rett syndrome: disintegration not dementia
Rett syndrome: EEG presentation
Rett syndrome: epidemiology and geographical variability
Rett syndrome: epidemiology and nosology - Progress in knowledge 1986 - A conference communication
Rett syndrome: evidence for normal dopaminergic function
Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations
Rett syndrome: eye pointing - A way of communication
Rett syndrome: findings suggesting axonopathy and mitochondrial abnormalities
Rett syndrome: from discovery to current interest
Rett syndrome: from gene to gesture
Rett syndrome: genetic breakthrough
Rett syndrome: genetic clinical study [Translation]
Rett syndrome: genetic clues based on mitochondrial changes in muscle
Rett syndrome: genetic horizons. Report on a satellite symposium at the 3rd Congress of the European Paediatric Neurology Society Nice, November, 1999
Rett syndrome: geographic variation in prevalence in Norway
Rett syndrome: guidance for therapists
Rett syndrome: habilitation and management reviewed
Rett syndrome: immunological studies
Rett syndrome: individual variability in developmental and behavioral characteristics and psychosocial pressure [Translation]
Rett syndrome: information, implications and strategies, for educators
Rett syndrome: initial experience with an emerging clinical entity
Rett syndrome: investigation of nine patients, including PET scan
Rett syndrome: lack of association with fragile site Xp22 and strategy for genetic mapping of X-linked new mutations
Rett syndrome: meeting the challenge of this gender-specific neurodevelopmental disorder
Rett syndrome: Methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations
Rett syndrome: natural history and management
Rett syndrome: natural history and underlying disease mechanisms
Rett syndrome: natural history, the stages and the clinical variability
Rett syndrome: neurobiological changes underlying specific symptoms
Rett syndrome: new observations
Rett syndrome: new progress towards the molecular basis of an enigmatic disorder
Rett syndrome: of girls and mice. Lessons for regression in autism
Rett syndrome: parents' views about specific symptoms
Rett syndrome: photographic evidence of rapid regression
Rett syndrome: positron emission tomography (PET) studies
Rett syndrome: positron emission tomography metabolic-clinical correlates
Rett syndrome: potential gene sources - phenotypical variability
Rett syndrome: presumptive carriers of the gene defect - Sex ratio among their siblings
Rett syndrome: progressive neurodegeneration or neuronal develomental defect?: prevalence, clinic and pathogenesis [Translation]
Rett syndrome: qualitative and quantitative differentiation from autism
Rett syndrome: questions and answers [Translation]
Rett syndrome: questions and answers [Translation]
Rett syndrome: random X chromosome inactivation
Rett syndrome: randomized controlled trial of L-carnitine
Rett syndrome: recent progress and implications for research and clinical practice
Rett syndrome: report of 7 cases [Translation]
Rett syndrome: report of 8 cases
Rett syndrome: report of electroencephalographic patterns with a clinical study [Translation]
Rett syndrome: retrospective and prospective study of 28 patients [Translation]
Rett syndrome: review and discussion of current diagnostic criteria
Rett syndrome: review of biological abnormalities
Rett syndrome: search for the molecular genetic defect on the X chromosome
Rett syndrome: significant clinical overlap with Angelman syndrome but not with methylation status
Rett syndrome: single-photon emission computed tomographic scan abnormalities, changes with age, and seizure activity
Rett syndrome: some behavioural aspects and an overview
Rett syndrome: some comments on terminology and diagnosis
Rett syndrome: spinal cord neuropathology
Rett syndrome: stimulation of endogenous biogenic amines
Rett syndrome: studies of 13 affected girls
Rett syndrome: summary of scientific findings to date
Rett syndrome: Swedish approach to analysis of prevalence and cause
Rett syndrome: the bcl-2 gene - A mediator of neurotrophic mechanisms?
Rett syndrome: the complex nature of a monogenic disease
Rett syndrome: the effects of upper extremity splints on stereotypic hand movements
Rett syndrome: the evolving picture of a disorder of brain development
Rett syndrome: the influence of dysregulated gene slicing
Rett syndrome: the late infantile regression period - A retrospective analysis of 91 cases
Rett syndrome: the nature of the disorder
Rett syndrome: the Swedish genealogic research project: new data and present position
Rett syndrome: update of a 25 year follow-up investigation in Western Sweden - sociomedical aspects
Rett syndrome: what do we know about it?
Rett syndrome--A gray matter disease? Electrophysiologic evidence
Rett syndrome--a nosological entity
Rett syndrome--a rare and often misdiagnosed syndrome: case report
Rett syndrome--a review and discussion of syndrome delineation and syndrome definition
Rett syndrome--a specific autistic disturbance [Translation]
Rett syndrome--an early catecholamine and indolamine deficient disorder?
Rett syndrome--an odd handicap affecting girls. A current 25-year follow-up in Western Sweden [Translation]
Rett syndrome--case report [Translation]
Rett syndrome--clinical studies [Translation]
Rett syndrome--clinical studies and pathophysiological consideration
Rett syndrome--from a healthy infant to a disabled woman [Translation]
Rett syndrome--mostly an unsolved mystery [Translation]
Rett syndrome--natural history in 70 cases
Rett syndrome--observational study of 33 families
Rett syndrome--search for genetic markers
Rett syndrome--two case reports
Rett variants - Rettoid phenotypes
Rett variants: a suggested model for inclusion criteria
RettBASE: The IRSA MECP2 variation database-a new mutation database in evolution
Rett-Info
Rett-like syndrome in fragile X syndrome
Retts linked to opioids, but cause still a mystery
Rett's syndrome
Rett's syndrome
Rett's syndrome
Rett's syndrome
Rett's syndrome
Rett's syndrome - A neurodevelopmental disorder : report of two cases
Rett's syndrome : a case report
Rett's syndrome [Translation]
Rett's syndrome [Translation]
Rett's syndrome [Translation]
Rett's syndrome [Translation]
Rett's syndrome and ornithine carbamoyltransferase deficiency
Rett's syndrome and ornithine carbamoyltransferase deficiency
Rett's syndrome and the long QT interval [Translation]
Rett's syndrome following bronchopneumonia
Rett's syndrome from the pediatrician's viewpoint [Translation]
Rett's syndrome in a boy
Rett's syndrome in an Australian child
Rett's syndrome in children : (Review of literature) [Translation]
Rett's syndrome in children [Translation]
Rett's syndrome in Korea--report of two cases
Rett's syndrome in the Spanish population [Translation]
Rett's syndrome in the West of Scotland
Rett's syndrome with Lennox-Gastaut pattern
Rett's syndrome. A new clinical picture [Translation]
Rett's syndrome. Clinical features and advances in genetics [Translation]
Rett's syndrome. Correlation of electroen-cephalographic characteristics with clinical staging
Rett's syndrome. Presentation of 2 cases [Translation]
Rett's syndrome: a case study
Rett's syndrome: a neurophysiological study
Rett's syndrome: a pervasive developmental disorder
Rett's syndrome: a progressive developmental disability in girls
Rett's syndrome: a progressive neurological disorder in girls
Rett's syndrome: a variant of Heller's dementia?
Rett's syndrome: analysis of the 1st 5 cases diagnosed in Brazil [Translation]
Rett's syndrome: cerebrospinal fluid biogenic amine levels correlate with motor dysfunction
Rett's syndrome: characterisation of respiratory patterns and sleep
Rett's syndrome: clinical analysis of a case report [Translation]
Rett's syndrome: clinical description and differential diagnosis [Translation]
Rett's syndrome: description of a case with abnormal respiratory pattern [Translation]
Rett's syndrome: diagnostic issues [Translation]
Rett's syndrome: opportunity for Australian study
Rett's syndrome: pathophysiology and anesthesiologic implications, represented by means of a case example [Translation]
Rett's syndrome: polygraphic electroencephalo-graphic-video characterisation of sleep and res-piratory patterns during sleep and wakefulness
Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls
Rett's syndrome: progression of symptoms from infancy to childhood
Rett's syndrome: report of 5 cases in Tunisia [Translation]
Rett's syndrome: study of 15 cases [Translation]
Rett's syndrome--differential diagnosis of autism in a case report [Translation]
Rett's syndrome--spindle activity analysis in NREM sleep
Revealing the roots of the Rett disorder
Review and meta-analysis of systematic searches for uniparental disomy (UPD) other than UPD 15
Review article: breaking new ground with Rett syndrome
Review of Rett syndrome
Review of the early clinical evidence for the underlying abnormality in Rett syndrome
Review of the Rett syndrome with a theory of autism
Ritanserin in autistic children [Translation]
Role of chromatin structure and transcriptional regulation in neurological disease
Role of mitochondrial lesion in pathogenesis of sporadic rett syndrome [Translation]
Role of monoaminergic systems in Rett syndrome
Role of nerve growth factor (NGF) in the pathophysiology of Rett syndrome
Role of the International Rett Syndrome Association
RS (Real Specialists) success panel
RS News
RS101
RS101
RS101: Getting to the roots
Rules for lifting [Translation]
Satellite associations in trisomy 21 [Translation]
Scientists create first animal model of Rett syndrome
Scoliosis - Natural history and treatment
Scoliosis and orthopaedic management
Scoliosis in Rett syndrome
Scoliosis in Rett syndrome
Scoliosis in Rett syndrome: clinical and biological aspects
Scoliosis in Rett syndrome: study of 18 cases
Scoliosis in the British Isles Rett Survey
Scoliosis in the Rett syndrome
Scoliosis in the Rett syndrome: natural history and treatment
Scoliosis: the postural approach to early intervention
Screening for mutations in the MECP2 (Rett syndrome) gene in Gilles de la Tourette syndrome
Screening of MECP2 coding sequence in patients with phenotypes of decreasing likelihood for Rett syndrome: a cohort of 171 cases
Screening tools assist with diagnosis of autistic spectrum disorders
Search for mutations in the GdX gene in Rett syndrome
Search for X-chromosomal microdeletions in Rett syndrome
Segregation analysis of the X-chromosome in a family with Rett syndrome in two generations
Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease
Seizures
Seizures and breathing issues
Seizures versus non-seizures in Rett syndrome
Seizures, vacant spells and abnormal EEG
Selective changes in Rett syndrome neurochemistry: findings of normal dopaminergic and decreased cholinergic function
Selective dendritic alterations in the cortex of Rett syndrome
Self injurious behaviour in Rett syndrome
Self-care, hand use and communication abilities in females with Rett syndrome
Self-care, hand use and communication abilities in girls and adults with Rett Syndrome
Self-injurious behavior in Rett syndrome: interactions between features of Rett syndrome and operant conditioning
Sensory Evoked Potentials (SEP). Measuring method in scoliosis surgery [Translation]
Sensory stimulation in Rett girls [Translation]
Series of writings infans cerebropathicus. Bd. 1 [Translation]
Serotonin and breathing dysrhythmia in Rett syndrome
Serum iron status in Rett syndrome
Serum melatonin kinetics and long-term melatonin treatment for sleep disorders in Rett syndrome
Seven year old American Rett syndrome girl, Amanda Stotter, and her interaction with a computer program
Severe forms of early childhood autism: new approach of pathogenesis
Severe Sinus Bradycardia in a patient with Rett syndrome: a new cause for a pause?
Sexual differences in pervasive developmental disorders
Shift to righthandedness in Rett syndrome around age 7
Short fourth toes in Rett syndrome: a biological indicator
Should a syndrome be called by its correct name? The example of the preserved speech variant of Rett syndrome
Sibling panel
Siblings with Rett syndrome in a Turkish family
Silent Angels [Translation]
Silent angels. The Rett syndrome story
Silent souls. Rett syndrome robs speech and other skills from young girls. Rehab is an essential part of treatment
Simple adaptions for early literacy
Single photon emission computed tomography(SPECT) in Rett syndrome
Single-strand conformational polymorphism analysis of mtDNA in Rett syndrome
Six Rett syndrome girls at Woody Point special school, Queensland, Australia
Sixth international workshop on the fragile X and X-linked mental retardation
Sixty years of autism [Translation]
Skeletal abnormalities in Rett syndrome: have we found a dysmorphic marker?
Skeletal abnormalities in Rett syndrome: increasing evidence for dysmorphogenetic defects
Skeletal status in patients affected by Rett syndrome
Sleep disorder in Rett syndrome and melatonin treatment
Sleep dysfunction in Rett syndrome – A trial of melatonin
Sleep dysfunction in Rett syndrome: a trial of exogenous melatonin treatment
Sleep dysfunction in Rett syndrome: lack of age related decrease in sleep duration
Sleep in infantile autism [Translation]
Sleep patterns in children and young adults with mental retardation and severe behaviour disorders
Sleep, apnea, and seizures
Social and preventive measures for mentally handicapped children [Translation]
Social care and medical aid
Social facilitation of object-oriented hand use in a Rett syndrome variant girl: implications for partial preservation of an hypothesized specialized cerebral network
Social indicators and mortality in infants. Experts' interview with H. Czermak and A. Rett [Translation]
Social indicators and mortality in infants. Experts' interview with H. Czermak and A. Rett [Translation]
Social indicators and mortality in infants. Experts' interview with H. Czermak and A. Rett [Translation]
Solution structure of the matrix attachment region-binding domain of chicken MeCP2
Solution structure of the methyl-cpg binding domain of human mbd1 in complex with methylated dna
Somatic mosaicism for a MECP2 mutation associated with classic Rett syndrome in a boy
Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males
Somatosensory evoked potentials (SEP) in Rett syndrome evaluating cortical involvement using onset latency
Some problems in the genetics of X-linked mental retardation
Some remarks regarding the search for a genetic basis for Rett syndrome
Special education
Special education appeals tribunals
Special issue on Rett syndrome
Special pedagogical intervention regarding pupils with Rett syndrome [Translation]
Specific clinical and psychological aspects of the organic psycho-syndrome in childhood brain damage [Translation]
Specific Rett areas in Italy. Study of 53 family trees
Spectrum and distribution of MECP2 mutations in 60 Italian Rett syndrome patients: tentative genotype/phenotype correlation
Spectrum and distribution of MECP2 mutations in 64 Italian Rett syndrome girls: tentative genotype/phenotype correlation
Spectrum of MECP2 mutations in Rett syndrome
Spectrum of MECP2 mutations in Rett syndrome
Spectrum of mutations in the MECP2 gene in patients with infantile autism and rett syndrome
Speech and language development in Rett syndrome: literature review and case study
Speech and motor disorders in Rett syndrome [Translation]
Speech and motor disturbances in Rett syndrome
Speech therapy
Speechless yet communicative: revealing the person behind the disability of Rett syndrome through clinical research on songs in music therapy
Speechless: facilitating communication for people without voices
Spinal fluid 5-methyltetrahydrofolate levels are normal in Rett syndrome
Splicing mutation associated with Rett syndrome and an experimental approach for genetic diagnosis
Sporadic Rett patients: prevalence of inherited versus de novo MECP2 mutations
Springboard for communication
Statement of the importance of music therapy
Statement on the importance of hydrotherapy
Statements and annual reviews
Storybook based communication intervention with girls with Rett syndrome
Storybook-based communication intervention for girls with Rett syndrome and their mothers
Strategies and techniques to support early literacy learning
Stress and family functioning in parents of girls with Rett syndrome
Stress in the family of the Rett's girl
Stress levels experienced by the parents of enterally fed children
Structural basis for APPTPPPLPP peptide recognition by the FBP11WW1 domain
Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome
Studies on mitochondrial pathogenesis of Rett syndrome: ultrastructural data from skin and muscle biopsies and mutational analysis at mtDNA nucleotides 10463 and 2835
Studies on the 3-dimensional architecture of dendritic spines and varicosities in human cortex by confocal laser scanning microscopy and Lucifer yellow microinjections
Studies on the ammonia content in the serum of children with brain damage with special reference to hyperammonemia [Translation]
Studies on the Rett syndrome. Part 1 : prevalence of the Rett syndrome [Translation]
Studies on the Rett syndrome. Part 2: polysomnographic and neuroendocrinological studies [Translation]
Studies to understand the pathophysiology of Rett syndrome
Study of auditive perception in sisters with Rett syndrome [Translation]
Study of cardiac and paroxysmal abnormalities in Rett syndrome
Study of correlations between epileptic events and paroxystic EEG anomalies in Rett syndrome
Study of MECP2 gene in Rett syndrome variants and autistic girls
Study of the conservative physiotherapy of scoliosis in the Rett syndrome [Translation]
Study of the pathogenesis of Rett syndrome
Study on Rett syndrome in Flanders; method: observation of patients
Subgroups in autism: are there behavioural phenotypes typical of underlying medical conditions?
Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome
Substance P immunoreactivity in Rett syndrome
Substance P immunoreactivity in the enteric nervous system in Rett syndrome
Substance P-mediated modulation of pacemaker properties in the mammalian respiratory network
Sudden death and cardiac arrhythmias in Rett syndrome
Sudden death in Rett syndrome [Translation]
Sulci digitales palmares in patients with Rett syndrome [Translation]
Summary of scientific findings to date
Support of Rett children and family: role of parent's association [Translation]
Supporting communication for females with Rett syndrome
Supporting communication of girls with Rett syndrome and their mothers in storybook reading
Surgical treatment of cerebral spastic paresis in children [Translation]
Surgical treatment of scoliosis in Rett syndrome
Survey of adolescents with severe intellectual handicap
Survey of MeCP2 in the Rett syndrome and the non-Rett syndrome brain
Survival in a large cohort of US girls and women with Rett syndrome
Swedish experiences with therapy in Rett syndrome
Symposium on congenital malformations. Introduction [Translation]
Syndrome identification case report # 148: a Rett-like syndrome with facial and limb anomalies
Syndrome of microcephaly, mental retardation, and tracheoesophageal fistula associated with features of Rett syndrome
Syndrome of microcephaly, tracheoesophageal fistula and mental retardation associated with features of Rett syndrome: a contiguous gene syndrome?
Syndromes and mental disability: Angelman, Prader-Willi and Rett
Syndromes of disordered chromatin remodeling
Syndromic autism: II. Genetic syndromes associated with autism [Translation]
Tachyarrhythmia as the first manifestation in a classic Rett syndrome [Translation]
Take care ... A guide for care-givers on how to improve their self-care
Teaching children with Rett syndrome to request preferred objects using aided communication: two preliminary studies
Teaching self-feeding skills to patients with Rett syndrome
Teeth grinding project
Telescoping intramedullary rodding with Bailey-Dubow nails for recurrent pathologic fractures in children without osteogenesis imperfecta
Temporal and regional differences in the olfactory proteome as a consequence of MeCP2 deficiency
Terminal deletion of (1)(q42) and its phenotypical manifestations
Testing for the gene
Tetrahydrobiopterin metabolism in the Rett disease
The A140V mutation in the MECP2 gene is not a common etiological factor among Brazilian mentally retarded males
The allopurinol test in patients with Rett syndrome
The art and science of music therapy: a handbook
The autistic spectrum: subgroups, boundaries, and treatment
The autistic-spectrum disorders
The Autonomic Project
The basics of genetics
The biological functions of the methyl-CpG-binding protein MeCP2 and its implication in Rett syndrome
The borderline of autism and Rett syndrome: five case histories to highlight diagnostic difficulties
The brain-damaged child. Medical, pedagogical and social problems [Translation]
The brain-damaged child--concept and definition [Translation]
The burden disability in Rett syndrome. Can we quantify it?
The care of mentally defective children [Translation]
The care of our children in everyday life
The central and peripheral autonomic nervous system and possible implications in Rett syndrome patients
The central autonomic disturbance in Rett syndrome
The child with Rett syndrome
The cholinergic basal forebrain system during development and its influence on cognitive processes: important questions and potential answers
The chromosomal aberration; clinical, psychological and biochemical problems in Down syndrome [Translation]
The clinical and neurophysiological aspects of Rett's syndrome [Translation]
The clinical pattern of the Rett syndrome
The clinical phenomenology of Rett's syndrome [Translation]
The clinical recognition and differential diagnosis of Rett syndrome
The clinical, neurophysiological and differential diagnostic aspects in a study of severe forms of early childhood autism [Translation]
The conduction system in Rett syndrome
The diagnosis and classification of the Rett syndrome in clinical and epidemiologic research
The diagnosis of Rett syndrome
The diagnostic value of the EEG in Angelmann and Rett syndrome at a young age
The discovery of the Rett gen: history and perspectives
The DNA methyltransferases of mammals
The EEG correlates of motor function in girls with Rett syndrome
The effect of chiropractic care on Rett syndrome: A case report
The effect of hand splints on stereotypic hand behavior in Rett's syndrome
The effect of the presentation of visual and auditory stimuli on the breathing patterns of two girls with Rett syndrome
The effect of vibroacoustic therapy in the treatment of Rett syndrome
The effects of neonatal basal forebrain lesions on cognition: towards understanding the developmental role of the cholinergic basal forebrain
The effects of presession exposure to attention on the results of assessments of attention as a reinforcer
The electroencephalogram in Rett syndrome
The electroencephalogram in Rett syndrome: correlation with hand movements
The epidemiology and public health significance of Rett syndrome
The epileptic child in the family and school [Translation]
The equipment maze
The expression of methyl CpG binding factor MeCP2 correlates with cellular differentiation in the developing rat brain and in cultured cells
The face of inclusion - A parent's perspective
The flow back of stomach contents to oesophagus [Translation]
The future for Rett girls
The future for Rett girls [Translation]
The G-button
The gene discovery
The genetic basis of Rett syndrome
The genetic basis of Rett syndrome: candidate gene considerations
The genetics of autism
The genetics of Rett syndrome
The genetics of Rett syndrome
The genetics of Rett syndrome: clues from familial recurrences
The genetics of Rett syndrome: the consequences of a disorder where every case is a new mutation
The grass is always greener. Sibling panel
The hands, and the mind, pre- and post-regression, in the Rett syndrome
The history and challenge of Rett syndrome
The history of childhood as culture history. With a conversation of the author with Hubert Christian Ehalt [Translation]
The identification of twenty one SNPs in Xq and candidate gene analysis in Rett syndrome
The impact of MECP2 mutations in the expression patterns of Rett syndrome patients
The importance of Oesophageal reflux
The incidence and natural history of scoliosis in Rett syndrome
The indices of the thrombocyte serotonin system and of the nerve growth factor system in children with hereditary disorders of neuropsychic development [Translation]
The invisible enemy: fighting Rett syndrome
The ketogenic diet
The key to Amanda
The lost girls - Living with Rett syndrome
The main symptoms of Rett syndrome
The major form of MeCP2 has a novel N-terminus generated by alternative splicing
The making of "Silent Angels"
The management of Rett syndrome
The maturing Rett child
The mongol who becomes older [Translation]
The monoamine hypothesis in Rett syndrome
The morphological substrate for communication
The mystery of the Rett syndrome
The neurobiology of Rett syndrome
The neuropathology of Rett syndrome - Overview 1994
The neuropathology of Rett syndrome is pervasive throughout the brain
The neuropathology of the Rett syndrome
The nutritional aspects of Rett syndrome
The official parent's sourcebook on Rett syndrome. A revised and updated directory for the internet age
The olfactory model system and Rett and Kallmann syndromes. Sniffing out insights into brain development
The organic psychosyndrome at childrens' age. 8th International symposium on the brain-damaged child, Vienna, 29 and May 1970. [Translation]
The orthopedic management of Rett syndrome
The paradoxical role of methyl CpG-binding protein 2 (MeCP2) in Rett syndrome
The parent idea book
The pathophysiology of Rett syndrome from the standpoints of clinical characteristics and sleep studies
The pathophysiology of the Rett syndrome from the standpoint of polysomnography
The pathophysiology, medical management and dental implications of fragile X, Rett, and Prader-Willi syndromes
The pattern of growth failure in Rett syndrome
The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome
The potentially handicapping effects of Rett syndrome on the development of a child
The preserved speech variant of the Rett complex: a report of 8 cases
The preserved speech variant: a subgroup of the Rett complex: a clinical report of 30 cases
The prevalence and incidence of Rett syndrome in Australia
The prevalence of Rett syndrome and infantile autism in Chikugo District, the South Western area of Fukuoka prefecture, Japan
The prevalence of Rett syndrome in Fukui prefecture
The proceedings of the 4th international symposium on Rett syndrome, Vienna, October 2-5, 1986
The proceedings of the 5th international conference on the Rett syndrome, Vienna, November 4-7, 1988. Dedicated to Professor Andreas Rett
The relationship of cumulative motor asymmetries to scoliosis in Rett syndrome
The relevance and value of music therapy for children with Rett syndrome
The Rett and Rett-like syndromes: a broad concept
The Rett condition - Broad clinical variability - A case report over three decades
The Rett disorder and the developing brain
The Rett foot: a biological indicator
The Rett girls with preserved speech
The Rett illness [Translation]
The Rett syndrome
The Rett syndrome
The Rett syndrome - Presentation and trial of a criticism - Basic principles for pedagogical and therapeutic treatment [Translation]
The Rett syndrome [Translation]
The Rett syndrome [Translation]
The Rett syndrome [Translation]
The Rett syndrome [Translation]
The Rett syndrome [Translation]
The Rett syndrome [Translation]
The Rett syndrome [Translation]
The Rett syndrome [Translation]
The Rett syndrome [Translation]
The Rett syndrome [Translation]
The Rett syndrome [Translation]
The Rett syndrome [Translation]
The Rett syndrome [Translation]
The Rett syndrome [Translation]
The Rett syndrome [Translation]
The Rett syndrome and CSF lactic acid patterns
The Rett syndrome and its meaning for the pedagogy of mentally handicapped people [Translation]
The Rett syndrome and ornithylcarbamoyl transferase deficiency
The Rett syndrome at the Antwerp Congress [Translation]
The Rett Syndrome Behaviour Questionnaire (RSBQ): refining the behavioural phenotype of Rett syndrome
The Rett syndrome bibliography III, 1989
The Rett syndrome complex: communicative functions in relation to developmental level and autistic features
The Rett syndrome handbook
The Rett syndrome in Flanders 1992
The Rett syndrome in males
The Rett syndrome in males
The Rett syndrome program project at Baylor College of Medicine
The Rett syndrome related to fragile X(P22) in caffeine-induced lymphocyte culture
The Rett syndrome, a genetic disease [Translation]
The Rett syndrome. A case report
The Rett syndrome. Present status and further prospects
The Rett syndrome. Symposium of the joint convention of the 5th international child neurology congress and the 3rd Asian and Oceanian congress of child neurology, Tokyo, November 4-9, 1990
The Rett syndrome. The speech therapeutical aspects of a 'new' syndrome [Translation]
The Rett syndrome: about 42 cases [Translation]
The Rett syndrome: an introductory overview 1990
The Rett syndrome: an overview
The Rett syndrome: autism, dementia and ataxia in progressive evolution in the girl [Translation]
The Rett syndrome: criteria of assessment and differential diagnosis [Translation]
The Rett syndrome: diagnostic criteria and remaining locomotor conduct [Translation]
The Rett syndrome: genetics and the future
The Rett syndrome: gross motor disability and neural impairment in adults
The Rett syndrome: magnetic resonance imaging and clinical findings in four girls
The Rett syndrome: note for physicians and therapists [Translation]
The Rett syndrome: progress report on studies at the Kennedy Institute
The Rett syndrome: proposed mechanism of genetic origin and inheritance
The Rett syndrome: the first case report from Pakistan
The Rett syndrome: the recent advances in genetic studies in the USA
The Rett syndrome--clinical presentation of the first 9 Albanian cases
The Rett syndrome--criteria and personal experience [Translation]
The Rett way [Translation]
The right to belong. The story of Yvonne
The role of different X-inactivation pattern on the variable clinical phenotype with Rett syndrome
The role of genetic and environmental factors in brain development
The role of the physician in the care of the child with Rett syndrome
The role of therapy in Rett syndrome
The role of X-chromosome inactivation in the manifestation of Rett syndrome
The search for disomy and/or skewed x-inactivation in carriers of x-linked diseases, in female monozygotic twin pairs, and in Rett syndrome
The Slovene Rett syndrome series
The so-called psychotropic effect of tegretol in the treatment of convulsions of cerebral origin in children
The spectrum and parental origin of de novo mutations of Methyl-CpG-binding protein 2(MECP2) in Rett syndrome
The spectrum of phenotypes in females with Rett syndrome
The surgical treatment of scoliosis in the Rett syndrome [Translation]
The surgical treatment of spinal deformities in Rett syndrome
The Swedish Rett Centre project
The Swedish Rett syndrome series updated March 1996. Geographical distribution at ages 3-19 years
The Swedish series of females with Rett syndrome 1960-92
The syndromes described by Kanner and Rett-Hagberg: overlap in an extended family
The tangled relationship of energy expenditure, energy intake, and body weight
The term 'restraints' is archaic
The therapist's role in the management of girls with Rett syndrome
The transcriptional repressor Mecp2 regulates terminal neuronal differentiation
The urea cycle in Rett syndrome
The use and effectiveness of elbow splints in the Rett syndrome
The use of assistive technology for symbol identification by children with Rett syndrome
The use of technology and computers with the Rett syndrome population
The usefulness of electroencephalography in Rett syndrome
The woman with Rett syndrome: program planning
The world of the autistic child: understanding and treating autistic spectrum disorders
Therapeutic effects of a ketogenic diet in Rett syndrome
Therapy in Rett syndrome
Therapy in Rett syndrome: drug trials and failures
Three decades of sociomedical experiences from West Swedish Rett females 4-60 years of age
Three Rett patients with both MECP2 mutation and 15q11-13 rearrangements
Three sisters with classic Rett syndrome
To know her is to love her
To learn better, keep the HAT on
To treating Rett syndrome: How to turn an everyday object into a helpful, child-friendly aid
Tokyo symposium on the Rett syndrome: neurobiological approach-concluding remarks and epilogue
Topiramate therapy in Rett syndrome
Toward the future
Towards a behavioral phenotype for Rett syndrome
Towards a full life with Rett disorder
Towards the genetic basis of Rett syndrome
Tracks and perspectives of child neurology in Japan. Interview by Toshiaki Abe [Translation]
Training program for children with the Rett syndrome [Translation]
Transcranial magnetic stimulation and early diagnosis of Rett syndrome
Transcranial magnetic stimulation and Rett syndrome [Translation]
Transcranial magnetic stimulation in patients with Down syndrome and Rolando-epilepsy confronted with patients with Rett syndrome [Translation]
Transcranial magnetic stimulation in patients with Rett syndrome: preliminary results
Transcriptional profiling in Rett syndrome using spotted cDNA microarrays
Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain
Transient improvement in seizures and EEG following carnitine
Transmission of skewed X-inactivation in familial Rett syndrome
Treating scoliosis in Rett syndrome
Treatment of hyperventilation in the Rett syndrome
Treatment of Rett's syndrome with bromocriptine
Trends in autism
Trisomy 21 and Rett syndrome: a double burden
Trisomy 21 associated with Rett syndrome phenotype
Two affected boys in a Rett syndrome family: clinical and molecular findings
Two affected males in a Rett syndrome family: clinical and molecular findings
Two brothers with male Rett syndrome
Two case studies of congenital disability
Two cases of trisomy 4p with translocation t(4p-,7q+) in several members of one family
Two new stars in the sky [Translation]
Two sisters affected by Rett syndrome
Two sisters with Rett syndrome
Ulrika
Ultrastructural examination of the axillary skin biopsy in the diagnosis of metabolic diseases
Ultrastructural study of enteric ganglia in three patients with Rett syndrome
Understanding constipation
Understanding Rett syndrome
Understanding Rett syndrome: a practical guide for parents, teachers, and therapists
Understanding Rett syndrome: a role for MeCP2 in neurons
Understanding your child with Rett syndrome: an approach to education
Understanding, recognizing and treating Rett syndrome
Unexplained osteopenia in Rett syndrome
Unusual EEG theta rhythms over central region in Rett syndrome: considerations of the underlying dysfunction
Upper extremity splinting in Rett syndrome
Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome
Urinary peptides in Rett syndrome
Use of a computer-based intervention for teaching girls with Rett syndrome to identify symbols
Use of an elbow restraint to improve finger-feeding skills in a child with Rett syndrome
Use of computers for teaching girls with Rett syndrome
Use of radiation hybrids and YAC clones in the efforts aimed at cloning the X chromosome breakpoint in a patient with Rett syndrome
Use of splints to develop hand skills in a woman with Rett syndrome
Using genetic epidemiology to study Rett syndrome: the design of a case-control study
Using mice to model cognitive deficits in neurologic disorders: narrowing in on Rett syndrome
Using the Internet to pilot a questionnaire on childhood disability in Rett syndrome
Vagus nerve stimulation for patients in residential treatment facilities
Valproate-induced hyperammonemic encephalopathy: imaging findings on diffusion-weighted MRI
Valproic acid-induced pancreatitis in childhood epilepsy: case series and review
Variation in exon 1 coding region and promoter of MECP2 in Rett syndrome and controls
Very long-chain fatty acids in Rett syndrome
Video feedback training: some effects on the stereotypic hand behavior of a girl with Rett syndrome
Vision in Rett syndrome: studies using evoked potential & event-related potentials
Vision, cognition and developmental characteristics of girls and women with Rett syndrome
Visual child neurology [Translation]
Visual function in Rett syndrome
Visual reaction patterns in Rett syndrome
Vitamin E serum levels in Rett syndrome
Voices of friendship
Volumetric neuroimaging in children with neurodevelopmental disorders--mapping the brain and behavior
We wither, we grow, we bloom
What can we learn from the electroencephalogram (EEG) in Rett syndrome?
What causes the Rett syndrome?
What does the diagnosis of Rett syndrome mean to parents?
What is known about autism : genes, brain, and behavior
What is Rett syndrome?
What is Rett syndrome? How can we adjust the day for the Rett girl? [Translation]
What is Rett's syndrome? 7-year clinical and electroencephalographic follow-up of a case [Translation]
When enough is enough: genetic diseases associated with transcriptional derepression
When the brain fails. Huda Zoghbi unravels the genetics of Rett syndrome and other disorders
Who is that girl with those beautiful eyes and where is she going? A view on research and education [Translation]
Why physical therapy?
Widened clinical spectrum of the Q128P MECP2 mutation in Rett syndrome
Women who make a difference
Working with schools to support early literacy learning
Workshop on autonomic function in Rett syndrome. Swedish Rett Center Froson, Sweden, May 1998
World congress on Rett syndrome [Translation]
Wrenching genes. New insights into a rare disorder may illuminate the biology behind a range of mental problems
X Chromosome inactivation in 30 girls with Rett syndrome: analysis using the probe
X chromosome inactivation patterns in brain in Rett syndrome: implications for the disease phenotype
X Chromosome linkage studies in familial Rett syndrome
X Chromosome mosaicism in Rett syndrome
X chromosome-inactivation patterns in patients with Rett syndrome
X inactivation in Rett syndrome patients
X Inactivation in Rett syndrome: a preliminary study showing partial preferential inactivation of paternal X with the M27B probe
X-Chromosome inactivation in Rett syndrome [Translation]
X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome.
X-chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain
X-Chromosome inactivation studies in females with Rett syndrome
X-Chromosome inactivation studies in Rett syndrome
X-Inactivation in girls with Rett syndrome
X-inactivation patterns in patients with Rett syndrome
You are not alone, for parents that just found out their child is disabled [Translation]
Your eyes speak to me [Translation]
Z score prediction model for assessment of bone mineral content in pediatric diseases
"Forme fruste" of Rett syndrome -- a case report
"Hallo Jessica!". Elementary music therapy with multiply disabled children according to the Rett syndrome model [Translation]
18q-Mosaicism associated with Rett syndrome phenotype
2 Clinical subgroups defined by the application of diagnostic criteria for Rett syndrome
2 year experience of clonazepam in childhood cerebral spasm seizures [Translation]
35 deaths in the British Survey; what can we learn?
4th International conference on Rett syndrome, Vienna, 1986 - A synopsis
5th International Conference on Rett syndrome - Vienna, Austria, November 1988