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SPINOCEREBELLAR ATAXIA 8

Known as: SCA8 
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
Background and purpose:  The ‘hot cross bun’ sign (HCBS), typically seen in the patients with multiple system atrophy, refers to… Expand
Review
2008
Review
2008
  • M. Manto
  • The Cerebellum
  • 2008
  • Corpus ID: 5311177
Spinocerebellar ataxias (SCAs) are a clinically heterogeneous group of disorders. Current molecular classification corresponds to… Expand
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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… Expand
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Highly Cited
2004
Highly Cited
2004
DNA tests in normal subjects and patients with ataxia and Parkinson's disease (PD) were carried out to assess the frequency of… Expand
Highly Cited
2001
Highly Cited
2001
The observation of large SCA8 alleles in healthy control subjects and nonataxic patients, together with a lack of segregation of… Expand
Highly Cited
2000
Highly Cited
2000
Objective: To compare the clinical and genetic features of the seven-generation family (MN-A) used to define the spinocerebellar… Expand
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Review
2000
Review
2000
Major advances have been made in the understanding of autosomal dominant cerebellar ataxias since genetic markers came into use… Expand
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Highly Cited
2000
Highly Cited
2000
We recently described an untranslated CTG expansion that causes a previously undescribed form of spinocerebellar ataxia (SCA8… Expand
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Highly Cited
2000
Highly Cited
2000
Spinocerebellar ataxia 8 (SCA8) is caused by a CTG repeat expansion in an untranslated region of a recently cloned gene on 13q21… Expand