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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… 
National Institutes of Health

Papers overview

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Review
2010
Review
2010
Interpretation of clinical trials comparing different drug regimens for Parkinson's disease (PD) is complicated by the different… 
Highly Cited
2004
Highly Cited
2004
From the Department of Neurology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts. Address… 
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… 
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… 
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… 
Highly Cited
1997
Review
1997
Review
1997
The autosomal recessive human disorder ataxia-telangiectasia (A-T) was first described as a separate disease entity 40 years ago… 
Highly Cited
1995
Highly Cited
1995
A POLYGLUTAMINE expansion (encoded by a CAG repeat) in specific proteins causes neurodegeneration in Huntington's disease (HD… 
Highly Cited
1975
Highly Cited
1975
ATAXIA telangiectasia (AT) is an autosomal recessive defect in man showing among the clinical features1 : cerebellar ataxia…