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GLAZE, DANIEL

One or more keywords matched the following items that are connected to GLAZE, DANIEL

Item Type	Name
Academic Article	Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome.
Academic Article	Rett syndrome: of girls and mice--lessons for regression in autism.
Academic Article	Vitamin D deficiency is prevalent in girls and women with Rett syndrome.
Academic Article	Gastrointestinal and nutritional problems occur frequently throughout life in girls and women with Rett syndrome.
Academic Article	Bone mineral content and bone mineral density are lower in older than in younger females with Rett syndrome.
Academic Article	A study of the treatment of Rett syndrome with folate and betaine.
Academic Article	Longevity in Rett syndrome: analysis of the North American Database.
Academic Article	Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities.
Academic Article	Autism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome.
Academic Article	Rett syndrome diagnostic criteria: lessons from the Natural History Study.
Academic Article	Growth failure and outcome in Rett syndrome: specific growth references.
Academic Article	Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males.
Academic Article	Rett syndrome: North American database.
Academic Article	Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
Academic Article	Gastrostomy placement improves height and weight gain in girls with Rett syndrome.
Academic Article	Profiling scoliosis in Rett syndrome.
Academic Article	Epilepsy and the natural history of Rett syndrome.
Academic Article	Rett syndrome: revised diagnostic criteria and nomenclature.
Academic Article	Clinical severity and quality of life in children and adolescents with Rett syndrome.
Concept	Methyl-CpG-Binding Protein 2
Academic Article	Brief report: MECP2 mutations in people without Rett syndrome.
Academic Article	Methyl-CpG-binding protein 2 (MECP2) mutation type is associated with disease severity in Rett syndrome.
Academic Article	Pubertal development in Rett syndrome deviates from typical females.
Academic Article	Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome.
Academic Article	The Changing Face of Survival in Rett Syndrome and?MECP2-Related Disorders.
Academic Article	Treatment of cardiac arrhythmias in a mouse model of Rett syndrome with Na+-channel-blocking antiepileptic drugs.
Academic Article	Improving Treatment Trial Outcomes for Rett Syndrome: The Development of Rett-specific Anchors for the Clinical Global Impression Scale.
Academic Article	Loss of MeCP2 Causes Urological Dysfunction and Contributes to Death by Kidney Failure in Mouse Models of Rett Syndrome.
Academic Article	Longitudinal course of epilepsy in Rett syndrome and related disorders.
Academic Article	Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2.
Academic Article	Scoliosis in Rett Syndrome: Progression, Comorbidities, and Predictors.
Academic Article	Behavioral profiles in Rett syndrome: Data from the natural history study.
Academic Article	The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2.
Academic Article	Biliary Tract Disease in Girls and Young Women With Rett Syndrome.
Academic Article	Hand stereotypies: Lessons from the Rett Syndrome Natural History Study.
Academic Article	Phenotypic features in MECP2 duplication syndrome: Effects of age.
Academic Article	Anthropometric Measures Correspond with Functional Motor Outcomes in Females with Rett Syndrome.
Academic Article	Exploring gastrointestinal health in MECP2 duplication syndrome.
Academic Article	Parental age effects and Rett syndrome.

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Methyl CpG Binding Protein 2