Spinocerebellar Ataxia Type 1

Known as: SCA1, Type 1 Spinocerebellar Ataxia, Cerebelloparenchymal Disorder Is 
 
National Institutes of Health

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Review
2009
Review
2009
Spinocerebellar ataxia type 1 (SCA1) is one of nine inherited neurodegenerative diseases caused by the expansion of a CAG… (More)
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Highly Cited
2008
Highly Cited
2008
OBJECTIVE To identify factors that determine disease severity and clinical phenotype of the most common spinocerebellar ataxias… (More)
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Highly Cited
2004
Highly Cited
2004
The dominant polyglutamine expansion diseases, which include spinocerebellar ataxia type 1 (SCA1) and Huntington disease, are… (More)
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Highly Cited
2003
Highly Cited
2003
Cognitive impairment was studied in distinct types of spinocerebellar ataxia (SCA): eleven SCA1, 14 SCA2, and 11 SCA3 individuals… (More)
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Highly Cited
2003
Highly Cited
2003
Spinocerebellar ataxia type 1 (SCA1) is one of several neurological disorders caused by a CAG repeat expansion. In SCA1, this… (More)
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Highly Cited
1998
Highly Cited
1998
Transgenic mice carrying the spinocerebellar ataxia type 1 (SCA1) gene, a polyglutamine neurodegenerative disorder, develop… (More)
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Review
1995
Review
1995
Spinocerebellar ataxia type 1 (SCA1) is a dominantly inherited neurodegenerative disorder characterized by ataxia, dysarthria and… (More)
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Highly Cited
1995
Highly Cited
1995
Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant neurodegenerative disorder caused by expansion of a GAG… (More)
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Highly Cited
1994
Highly Cited
1994
Spinocerebellar ataxia type 1 (SCA1) is a neurodegenerative disorder caused by expansion of a CAG trinucleotide repeat. In this… (More)
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Highly Cited
1993
Highly Cited
1993
Spinocerebellar ataxia type 1 (SCA1) is an autosomal dominant disorder characterized by neurodegeneration of the cerebellum… (More)
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