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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
10
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pubmed:dateCreated |
2001-11-27
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pubmed:abstractText |
A kindred is described with a dominantly inherited "pure" cerebellar ataxia in which the currently known spinocerebellar ataxias have been excluded. In the eight subjects studied, a notable clinical feature is slow progression, with the three least affected having only a mild degree of gait ataxia after three or more decades of disease duration. Pending an actual chromosomal locus discovery, the name spinocerebellar ataxia (SCA)15 is expectantly applied.
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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:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0028-3878
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
27
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pubmed:volume |
57
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1913-5
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:11723290-Adult,
pubmed-meshheading:11723290-Aged,
pubmed-meshheading:11723290-Atrophy,
pubmed-meshheading:11723290-Cerebellum,
pubmed-meshheading:11723290-Chromosome Aberrations,
pubmed-meshheading:11723290-Chromosome Mapping,
pubmed-meshheading:11723290-Female,
pubmed-meshheading:11723290-Genes, Dominant,
pubmed-meshheading:11723290-Genetic Linkage,
pubmed-meshheading:11723290-Genotype,
pubmed-meshheading:11723290-Humans,
pubmed-meshheading:11723290-Magnetic Resonance Imaging,
pubmed-meshheading:11723290-Male,
pubmed-meshheading:11723290-Middle Aged,
pubmed-meshheading:11723290-Neurologic Examination,
pubmed-meshheading:11723290-Pedigree,
pubmed-meshheading:11723290-Spinocerebellar Ataxias
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pubmed:year |
2001
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pubmed:articleTitle |
A new autosomal dominant pure cerebellar ataxia.
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pubmed:affiliation |
Genetic Health Services Victoria at the Alfred Hospital, Monash University, Alfred Hospital, Parkville, Melbourne, Australia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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