|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
5
|
|
pubmed:dateCreated |
2009-5-18
|
|
pubmed:abstractText |
Parkinson's disease (PD) has been related to mutations associated with spinocerebellar ataxias (SCA); the frequency of the diagnosis of these mutations is low in general late-onset PD cases. Our aim was to investigate a selected high-risk group of PD patients.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Jun
|
|
pubmed:issn |
1873-5126
|
|
pubmed:author |
|
|
pubmed:issnType |
Electronic
|
|
pubmed:volume |
15
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
374-8
|
|
pubmed:meshHeading |
pubmed-meshheading:18990604-Adult,
pubmed-meshheading:18990604-Age of Onset,
pubmed-meshheading:18990604-Antiparkinson Agents,
pubmed-meshheading:18990604-DNA Repeat Expansion,
pubmed-meshheading:18990604-Family,
pubmed-meshheading:18990604-Female,
pubmed-meshheading:18990604-Genes, Dominant,
pubmed-meshheading:18990604-Genetic Variation,
pubmed-meshheading:18990604-Humans,
pubmed-meshheading:18990604-Levodopa,
pubmed-meshheading:18990604-Machado-Joseph Disease,
pubmed-meshheading:18990604-Male,
pubmed-meshheading:18990604-Middle Aged,
pubmed-meshheading:18990604-Nerve Tissue Proteins,
pubmed-meshheading:18990604-Nuclear Proteins,
pubmed-meshheading:18990604-Parkinson Disease,
pubmed-meshheading:18990604-Pedigree,
pubmed-meshheading:18990604-Phenotype,
pubmed-meshheading:18990604-Repressor Proteins,
pubmed-meshheading:18990604-Spinocerebellar Degenerations
|
|
pubmed:year |
2009
|
|
pubmed:articleTitle |
Intrafamilial variability of Parkinson phenotype in SCAs: novel cases due to SCA2 and SCA3 expansions.
|
|
pubmed:affiliation |
Medical Sciences, Postgraduate Program, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
|
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
