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… (More)

Topic mentions per year

Topic mentions per year

1935-2018
020040019352017

Papers overview

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Review
2016
Review
2016
BACKGROUND Aside from idiopathic Parkinson syndrome (Parkinson's disease), there are a number of other, so-called atypical… (More)
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Review
2014
Review
2014
BACKGROUND AND PURPOSE To assess, through systematic review, distinctive or common clinical signs of autosomal dominant… (More)
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Highly Cited
2006
Highly Cited
2006
Episodic ataxia type-2 (EA2) is caused by mutations in P/Q-type voltage-gated calcium channels that are expressed at high… (More)
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Highly Cited
2004
Highly Cited
2004
Malfunctions of potassium channels are increasingly implicated as causes of neurological disorders. However, the functional roles… (More)
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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… (More)
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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… (More)
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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… (More)
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Highly Cited
1996
Highly Cited
1996
Genes for familial hemiplegic migraine (FHM) and episodic ataxia type-2 (EA-2) have been mapped to chromosome 19p13. We… (More)
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Highly Cited
1996
Highly Cited
1996
1. We studied seven subjects with cerebellar lesions and seven control subjects as they made reaching movements in the sagittal… (More)
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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… (More)
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