|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
6
|
|
pubmed:dateCreated |
1993-6-3
|
|
pubmed:abstractText |
A family is described in which closely consanguineous parents had Huntington chorea and in their son a severe hypertonic-hypokinetic syndrome with pellagra-like cutaneous changes was present. In two generations of the family in 6 subjects involuntary movements and gait disorders were reported.
|
|
pubmed:language |
pol
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:status |
MEDLINE
|
|
pubmed:issn |
0028-3843
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
26
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
873-7
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:1301515-Adult,
pubmed-meshheading:1301515-Aged,
pubmed-meshheading:1301515-Consanguinity,
pubmed-meshheading:1301515-Family,
pubmed-meshheading:1301515-Family Health,
pubmed-meshheading:1301515-Female,
pubmed-meshheading:1301515-Gait,
pubmed-meshheading:1301515-Hospitalization,
pubmed-meshheading:1301515-Hospitals, Psychiatric,
pubmed-meshheading:1301515-Humans,
pubmed-meshheading:1301515-Huntington Disease,
pubmed-meshheading:1301515-Male,
pubmed-meshheading:1301515-Mental Disorders,
pubmed-meshheading:1301515-Middle Aged,
pubmed-meshheading:1301515-Polymorphism, Genetic
|
|
pubmed:articleTitle |
[Contribution to the clinical polymorphism in Huntington's disease].
|
|
pubmed:affiliation |
II Katedry i Kliniki Neurologii Sl. AM, Zabrzu.
|
|
pubmed:publicationType |
Journal Article,
English Abstract
|
