Ataxias, Hereditary

Known as: Spinocerebellar Degeneration, Hereditary, Degeneration, Familial Spinocerebellar, Degenerations, Inherited Spinocerebellar 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1950-2017
0519502016

Papers overview

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2011
2011
Spinocerebellar ataxias 6 and 7 (SCA6 and SCA7) are neurodegenerative disorders caused by expansion of CAG repeats encoding… (More)
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2011
2011
The differential diagnosis for hereditary ataxia encompasses a variety of diseases characterized by both autosomal dominant and… (More)
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2004
2004
Delay eyeblink conditioning was examined in patients with genetically-defined heredoataxias and age-matched control subjects. 24… (More)
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2003
2003
In the present study the olfactory system of hereditary ataxia patients was tested using the smell identification test. Two… (More)
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2002
2002
Autosomal dominant spinocerebellar ataxias (SCAs) are a clinical and molecular heterogeneous group of neurodegenerative disorders… (More)
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2001
2001
Gluten sensitivity, with or without classical celiac disease symptoms and intestinal pathology, has been suggested as a… (More)
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2001
2001
INTRODUCTION The hereditary ataxias in Cuba make up the highest concentration of these patients in the world. The spinocerebellar… (More)
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2000
2000
Expansion of CTG/CAG trinucleotide repeats has been shown to cause a number of autosomal dominant cerebellar ataxias (ADCA) such… (More)
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1998
1998
OBJECTIVE To identify and to characterize sleep disturbances in patients with hereditary ataxias. BACKGROUND We observed… (More)
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1980
1980
In a previously unreported family with olivopontocerebellar atrophy, the kindred contained over 600 individuals in five… (More)
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