Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2010-3-16
pubmed:abstractText
Rett syndrome (RTT) is a neurodevelopmental disorder primarily seen in females, most with a mutation in MECP2. Epilepsy has been reported in 50%-80%. Previous reports were based on small sample sizes or parent-completed questionnaires, or failed to consider the impact of specific MECP2 mutations.
pubmed:grant
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1526-632X
pubmed:author
pubmed:issnType
Electronic
pubmed:day
16
pubmed:volume
74
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
909-12
pubmed:dateRevised
2011-7-26
pubmed:meshHeading
pubmed-meshheading:20231667-Adolescent, pubmed-meshheading:20231667-Adult, pubmed-meshheading:20231667-Age Factors, pubmed-meshheading:20231667-Age of Onset, pubmed-meshheading:20231667-Child, pubmed-meshheading:20231667-Child, Preschool, pubmed-meshheading:20231667-Epilepsy, pubmed-meshheading:20231667-Female, pubmed-meshheading:20231667-Genetic Predisposition to Disease, pubmed-meshheading:20231667-Humans, pubmed-meshheading:20231667-Infant, pubmed-meshheading:20231667-Male, pubmed-meshheading:20231667-Methyl-CpG-Binding Protein 2, pubmed-meshheading:20231667-Middle Aged, pubmed-meshheading:20231667-Phenotype, pubmed-meshheading:20231667-Regression Analysis, pubmed-meshheading:20231667-Rett Syndrome, pubmed-meshheading:20231667-Severity of Illness Index, pubmed-meshheading:20231667-Sex Factors, pubmed-meshheading:20231667-Young Adult
pubmed:year
2010
pubmed:articleTitle
Epilepsy and the natural history of Rett syndrome.
pubmed:affiliation
The Blue Bird Circle Rett Center, Baylor College of Medicine, Houston, TX 77030, USA. dglaze@bcm.edu
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural