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rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
10
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pubmed:dateCreated |
2001-3-13
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|
pubmed:abstractText |
Recently the clinical and genetic investigation of cerebellar diseases has experienced an extraordinary advance due to localization of the disorders in different chromosomal loci. This type of investigation has been done in Peru in the last decade, studying a Peruvian family from the Huarochiri province.
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pubmed:language |
spa
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pubmed:journal |
|
|
pubmed:citationSubset |
IM
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|
pubmed:status |
MEDLINE
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pubmed:issn |
0210-0010
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
31
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
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pubmed:pagination |
923-8
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pubmed:dateRevised |
2009-5-28
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pubmed:meshHeading |
pubmed-meshheading:11244684-Adult,
pubmed-meshheading:11244684-Aged,
pubmed-meshheading:11244684-Atrophy,
pubmed-meshheading:11244684-Brain Stem,
pubmed-meshheading:11244684-Cerebellum,
pubmed-meshheading:11244684-Chromosomes, Human, Pair 3,
pubmed-meshheading:11244684-Cognition Disorders,
pubmed-meshheading:11244684-Female,
pubmed-meshheading:11244684-Functional Laterality,
pubmed-meshheading:11244684-Humans,
pubmed-meshheading:11244684-Magnetic Resonance Angiography,
pubmed-meshheading:11244684-Male,
pubmed-meshheading:11244684-Middle Aged,
pubmed-meshheading:11244684-Optic Nerve,
pubmed-meshheading:11244684-Pedigree,
pubmed-meshheading:11244684-Peru,
pubmed-meshheading:11244684-Severity of Illness Index,
pubmed-meshheading:11244684-Spinocerebellar Ataxias,
pubmed-meshheading:11244684-Tomography, X-Ray Computed,
pubmed-meshheading:11244684-Trinucleotide Repeat Expansion,
pubmed-meshheading:11244684-Vision Disorders,
pubmed-meshheading:11244684-Wechsler Scales
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pubmed:articleTitle |
[Clinical and genetic studies of a family from Peru affected by spinocerebellar ataxia type 7].
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|
pubmed:affiliation |
Departamento de Neurología, Hospital Nacional Dos de Mayo, Lima, Perú. hgarcia@pol.com.pe
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pubmed:publicationType |
Journal Article,
English Abstract,
Case Reports
|
