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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 a… Expand
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Review
2008
Review
2008
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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2004
2004
DNA tests in normal subjects and patients with ataxia and Parkinson's disease (PD) were carried out to assess the frequency of… Expand
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2003
2003
OBJECTIVES To determine the frequencies of spinocerebellar ataxias (SCAs) in the Kinki district, the western part of the main… Expand
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2001
2001
Background: The autosomal dominant cerebellar ataxias (ADCA) are a clinically heterogeneous group of disorders. The mutations for… Expand
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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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2000
2000
Spinocerebellar ataxia 8 (SCA8) is caused by a CTG repeat expansion in an untranslated region of a recently cloned gene on 13q21… Expand
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2000
2000
Autosomal dominant cerebeller ataxias (ADCAs) are a heterogeneous group of neurodegenerative disorders that differ in both the… Expand
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