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SPINOCEREBELLAR ATAXIA 8

Known as: SCA8 
National Institutes of Health

Related topics

Related topics

12 relations
ATXN8, (CAG)n EXPANSIONATXN8OS geneAbnormal pyramidal signsAutosomal dominant inheritance

Broader (1)

Spinocerebellar Degeneration

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2008
2008
Severe symptoms of 16q-ADCA coexisting with SCA8 repeat expansion
2006
2006
Atypical Parkinsonism and SCA8.
2005
2005
Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6.
BACKGROUND Dominantly inherited spinocerebellar ataxia (SCA) is a clinically and genetically heterogeneous group of… 
2002
2002
SCA8 in the Spanish population including one homozygous patient
Controversial data have been reported about SCA8 since its description in 1999. The most accepted hypothesis is that CTG… 
2002
2002
Calculating predictive values for the large repeat alleles at the SCA8 locus in patients with ataxia
Since the original description of SCA8 in 1999,1 several reports have been published on the occurrence of the SCA8 gene CTG… 
2002
2002
The vestibulo-ocular reflex and velocity storage in spinocerebellar ataxia 8.
The autosomal dominant spinocerebellar ataxias (SCAs) are a group of neurodegenerative diseases characterized by progressive… 
Highly Cited
2000
Highly Cited
2000
Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia
Review
2000
Review
2000
The molecular biology of the autosomal‐dominant cerebellar ataxias
Autosomal‐dominant cerebellar ataxias (ADCA) may present as progressive or paroxysmal disorders. While the progressive ataxias… 
1998
1998
A refined physical and EST map spanning 7.4 Mb of 10q24, a region involved in neurological disorders
Chromosome band 10q24 appears to be a gene-rich region, given the elevated number of expressed sequence tags (ESTs) already… 
Highly Cited
1997
Highly Cited
1997
Toward cloning of a novel ataxia gene: refined assignment and physical map of the IOSCA locus (SCA8) on 10q24.
Infantile onset spinocerebellar ataxia (IOSCA) is a progressive neurological disorder of unknown etiology. It is inherited as an… 
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