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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
15
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pubmed:dateCreated |
2007-4-10
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pubmed:abstractText |
Hand stereotypies are considered a hallmark of Rett syndrome (RTT) and are usually described as symmetric movements at the midline. However, related pathologies may show the same type of involuntary movement. Furthermore, patients with RTT also have stereotypies with other localizations that are less well characterized.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1526-632X
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pubmed:author |
pubmed-author:BarbosaCC,
pubmed-author:BarboyNN,
pubmed-author:BorgesLL,
pubmed-author:CabralAA,
pubmed-author:CabralPP,
pubmed-author:CaladoEE,
pubmed-author:CarrilhoII,
pubmed-author:DiasAA,
pubmed-author:DiazBB,
pubmed-author:EusébioFF,
pubmed-author:FonsecaMM,
pubmed-author:GomesRR,
pubmed-author:LevyAA,
pubmed-author:MacielPP,
pubmed-author:MiraGG,
pubmed-author:MonteiroJJ,
pubmed-author:MoreiraAA,
pubmed-author:OliveiraGG,
pubmed-author:OliveiraPP,
pubmed-author:SantosMM,
pubmed-author:SequeirosJJ,
pubmed-author:TemudoTT,
pubmed-author:VieiraJJ
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pubmed:issnType |
Electronic
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pubmed:day |
10
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pubmed:volume |
68
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1183-7
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:17420401-Adolescent,
pubmed-meshheading:17420401-Adult,
pubmed-meshheading:17420401-Child,
pubmed-meshheading:17420401-Child, Preschool,
pubmed-meshheading:17420401-Comorbidity,
pubmed-meshheading:17420401-DNA Mutational Analysis,
pubmed-meshheading:17420401-Female,
pubmed-meshheading:17420401-Genetic Predisposition to Disease,
pubmed-meshheading:17420401-Genetic Testing,
pubmed-meshheading:17420401-Heterozygote,
pubmed-meshheading:17420401-Humans,
pubmed-meshheading:17420401-Incidence,
pubmed-meshheading:17420401-Infant,
pubmed-meshheading:17420401-Male,
pubmed-meshheading:17420401-Methyl-CpG-Binding Protein 2,
pubmed-meshheading:17420401-Mutation,
pubmed-meshheading:17420401-Polymorphism, Single Nucleotide,
pubmed-meshheading:17420401-Portugal,
pubmed-meshheading:17420401-Prevalence,
pubmed-meshheading:17420401-Rett Syndrome,
pubmed-meshheading:17420401-Risk Assessment,
pubmed-meshheading:17420401-Risk Factors,
pubmed-meshheading:17420401-Stereotypic Movement Disorder
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pubmed:year |
2007
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pubmed:articleTitle |
Stereotypies in Rett syndrome: analysis of 83 patients with and without detected MECP2 mutations.
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pubmed:affiliation |
Unidade de Neuropediatria, Serviço de Pediatria, Hospital de Santo António, SA, Largo Abel Salazar, Porto, Portugal. teresatemudo@netcabo.pt
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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