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ataxic

Known as: ataxics 
 
National Institutes of Health

Papers overview

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Review
2018
Review
2018
Genetic prion diseases (gPrDs) caused by mutations in the prion protein gene (PRNP) have been classified as genetic Creutzfeldt… Expand
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Highly Cited
2011
Highly Cited
2011
Spinocerebellar ataxia type 3 (SCA3) is an autosomal dominant neurodegenerative disease caused by polyglutamine-expanded ataxin-3… Expand
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Highly Cited
2002
Highly Cited
2002
This study is the third in a series that has explored the source of intelligibility decrement in dysarthria by jointly… Expand
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Highly Cited
2000
Highly Cited
2000
Stargazer, an ataxic and epileptic mutant mouse, lacks functional AMPA (α-amino-3-hydroxyl-5-methyl-4-isoxazolepropionate… Expand
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Highly Cited
2000
Highly Cited
2000
To clarify the characteristics of parkinsonian and ataxic gaits, we analyzed electromyograms (EMGs) of the thigh and leg muscles… Expand
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Highly Cited
1996
Highly Cited
1996
Recently, we identified a novel gene, MJD1, which contains an expanded GAG triplet repeat in Machado–Joseph disease. Here we… Expand
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Highly Cited
1996
Highly Cited
1996
The cerebellar contribution to cognitive operations and emotional behavior is critically dependent upon the existence of… Expand
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Highly Cited
1996
Highly Cited
1996
NEURONS contain distinct compartments including dendrites, dendritic spines, axons and synaptic terminals1. The molecular… Expand
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Highly Cited
1975
Highly Cited
1975
The problem of whether ethanol damage or malnutrition is primary cause of cerebellar damage to developing central nervous sstems… Expand
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Highly Cited
1969
Highly Cited
1969
SOME TWO YEARS AGO we investigated a child with profound psychomotor retardation who had had an occipital meningoencephalocele… Expand
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