|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
1
|
|
pubmed:dateCreated |
2005-2-10
|
|
pubmed:abstractText |
Sporadic and hereditary ataxias (HA) represent a group of clinically and genetically heterogeneous syndromes characterized by spinocerebellar degeneration producing a motoneuron coordination disorder. In these diseases urinary and sexual symptoms are commonly associated to the neurological alterations.
|
|
pubmed:language |
spa
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:status |
MEDLINE
|
|
pubmed:issn |
0213-4853
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
20
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
17-23
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:15704017-Adolescent,
pubmed-meshheading:15704017-Adult,
pubmed-meshheading:15704017-Aged,
pubmed-meshheading:15704017-Aged, 80 and over,
pubmed-meshheading:15704017-Case-Control Studies,
pubmed-meshheading:15704017-Cross-Sectional Studies,
pubmed-meshheading:15704017-Female,
pubmed-meshheading:15704017-Female Urogenital Diseases,
pubmed-meshheading:15704017-Humans,
pubmed-meshheading:15704017-Male,
pubmed-meshheading:15704017-Male Urogenital Diseases,
pubmed-meshheading:15704017-Middle Aged,
pubmed-meshheading:15704017-Questionnaires,
pubmed-meshheading:15704017-Spinocerebellar Degenerations
|
|
pubmed:articleTitle |
[Urogenital alterations in hereditary and sporadic neurodegenerative ataxias].
|
|
pubmed:affiliation |
Servicio de Urología, Hospital de Móstoles, Madrid. jmdiezr@teleline.es
|
|
pubmed:publicationType |
Journal Article,
English Abstract
|
