Developmental delay in Rett syndrome: data from the natural history study. - Wikidata - wikimedia - TriplyDB

Developmental delay in Rett syndrome: data from the natural history study.

Developmental delay in Rett syndrome: data from the natural history study.

http://www.wikidata.org/entity/Q30585029

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Developmental Dynamics of Rett Syndrome Rett Syndrome: Crossing the Threshold to Clinical Translation MECP2 disorders: from the clinic to mice and back Targeted pharmacological treatment of autism spectrum disorders: fragile X and Rett syndromes Rett Syndrome: Reaching for Clinical Trials Unexpected cellular players in Rett syndrome pathology MECP2 regulates cortical plasticity underlying a learned behaviour in adult female mice Degraded neural and behavioral processing of speech sounds in a rat model of Rett syndrome.Treatment of cardiac arrhythmias in a mouse model of Rett syndrome with Na+-channel-blocking antiepileptic drugs.Age of diagnosis in Rett syndrome: patterns of recognition among diagnosticians and risk factors for late diagnosis.Anxiety-like behavior in Rett syndrome: characteristics and assessment by anxiety scales.The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders.Apoptotic Activity of MeCP2 Is Enhanced by C-Terminal Truncating Mutations.Progress in Rett Syndrome: from discovery to clinical trials Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2.From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2.Neurobiologically-based treatments in Rett syndrome: opportunities and challenges.Early development in Rett syndrome - the benefits and difficulties of a birth cohort approach.Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors.Detecting autonomic response to pain in Rett syndrome.Neurogenetics in Child Neurology: Redefining a Discipline in the Twenty-first Century.Behavioural biomarkers of typical Rett syndrome: moving towards early identification The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome.Motor, Somatosensory, Viscerosensory and Metabolic Impairments in a Heterozygous Female Rat Model of Rett Syndrome.Loss of skills and onset patterns in neurodevelopmental disorders: Understanding the neurobiological mechanisms.Comparing social reciprocity in preserved speech variant and typical Rett syndrome during the early years of life.MECP2 variation in Rett syndrome - an overview of current coverage of genetic and phenotype data within existing databases The roles of motor activity and environmental enrichment in intellectual disability.RettBASE: Rett syndrome database update.When Rett syndrome is due to genes other than MECP2.Parents' initial concerns about the development of their children later diagnosed with fragile X syndrome.Mutations in epilepsy and intellectual disability genes in patients with features of Rett syndrome.

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P2860

Developmental delay in Rett syndrome: data from the natural history study.

http://www.wikidata.org/entity/Q30585029

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2014 nî lūn-bûn

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2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2014 թվականի հուլիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Developmental delay in Rett syndrome: data from the natural history study.

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Developmental delay in Rett syndrome: data from the natural history study.

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Developmental delay in Rett syndrome: data from the natural history study.

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Developmental delay in Rett syndrome: data from the natural history study.

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Developmental delay in Rett syndrome: data from the natural history study.

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Journal of Neurodevelopmental Disorders

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Developmental delay in Rett syndrome: data from the natural history study.

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Alan K Percy

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Daniel G Glaze

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Fran Annese

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Hye-Seung Lee

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Jane B Lane

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Judy O Barrish

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Katherine Barnes

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Lauren McNair Baggett

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Steven A Skinner

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P2860

Rett syndrome: revised diagnostic criteria and nomenclature

Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome

Investigating genotype-phenotype relationships in Rett syndrome using an international data set.

Gross motor profile in rett syndrome as determined by video analysis.

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases.

On a unusual brain atrophy syndrome in hyperammonemia in childhood

Rett syndrome and associated movement disorders.

Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome

Clinical severity and quality of life in children and adolescents with Rett syndrome

Rett syndrome: model of neurodevelopmental disorders.

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Jeffrey L. Neul

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