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Cerebellar Ataxia

Known as: Ataxia, ATAXIA CEREBELLAR, Cerebellar ataxia NOS 
Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb… Expand
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2018
Review
2018
Voltage-gated calcium channels couple depolarization of the cell-surface membrane to entry of calcium, which triggers secretion… Expand
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Review
2010
Review
2010
Cerebellar ataxias with autosomal dominant transmission are rare, but identification of the associated genes has provided insight… Expand
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Review
2004
Review
2004
Autosomal dominant cerebellar ataxias are hereditary neurodegenerative disorders that are known as spinocerebellar ataxias (SCA… Expand
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Highly Cited
2004
Highly Cited
2004
From the Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts. Address… Expand
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Highly Cited
2003
Highly Cited
2003
We present a series of 26 patients, all >50 years of age, who are carriers of the fragile X premutation and are affected by a… Expand
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Highly Cited
2001
Highly Cited
2001
Genetic etiologies of at least 20% of autosomal dominant cerebellar ataxias (ADCAs) have yet to be clarified. We identified a… Expand
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Highly Cited
1997
Highly Cited
1997
Despite the involvement of cerebellar ataxia in a large variety of conditions and its frequent association with other… Expand
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Highly Cited
1997
Highly Cited
1997
A polymorphic CAG repeat was identified in the human α1A voltage-dependent calcium channel subunit. To test the hypothesis that… Expand
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Review
1997
Review
1997
The autosomal recessive human disorder ataxia-telangiectasia (A-T) was first described as a separate disease entity 40 years ago… Expand
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Highly Cited
1995
Highly Cited
1995
A POLYGLUTAMINE expansion (encoded by a CAG repeat) in specific proteins causes neurodegeneration in Huntington's disease (HD… Expand
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