SPINOCEREBELLAR ATAXIA 8

Known as: SCA8 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1999-2016
012319992016

Papers overview

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2011
2011
We administered a large battery of neuropsychological tests to an heterogeneous cohort of genetically defined spinocerebellar… (More)
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2009
2009
BACKGROUND AND PURPOSE The 'hot cross bun' sign (HCBS), typically seen in the patients with multiple system atrophy, refers to a… (More)
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2005
2005
OBJECTIVES Only a limited number of studies have investigated the cognitive performances of spinocerebellar ataxia (SCA) patients… (More)
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2005
2005
An increasing number of genetically defined types of spinocerebellar ataxia (SCA) have been reported in the past decade… (More)
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Highly Cited
2004
Highly Cited
2004
Spinocerebellar Ataxia 8 (SCA8) appears unique among triplet repeat expansion-induced neurodegenerative diseases because the… (More)
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2003
2003
Spinocerebellar Ataxia 8 (SCA8) is a neurodegenerative disorder caused by expansion of a trinucleotide repeat. We undertake a… (More)
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2002
2002
BACKGROUND Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia… (More)
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2001
2001
The observation of large SCA8 alleles in healthy control subjects and nonataxic patients, together with a lack of segregation of… (More)
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2000
2000
OBJECTIVE To compare the clinical and genetic features of the seven-generation family (MN-A) used to define the spinocerebellar… (More)
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2000
2000
Spinocerebellar ataxia 8 (SCA8) is caused by a CTG repeat expansion in an untranslated region of a recently cloned gene on 13q21… (More)
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