Spinocerebellar Ataxia Type 2

Known as: Cerebellar Degeneration with Slow Eye Movements, Type 2 Spinocerebellar Ataxia, IIs, Spinocerebellar Atrophy 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1992-2018
010203019922018

Papers overview

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Highly Cited
2009
Highly Cited
2009
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominantly inherited, neurodegenerative disease caused by an expansion of… (More)
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2008
2008
To study the use of transcranial brain parenchyma sonography (TCS), in particular the echogenic signal in the substantia nigra… (More)
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2007
2007
Patients with spinocerebellar ataxia type 2 (SCA2), develop severe pontine nuclei, inferior olives, and Purkinje cell… (More)
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2006
2006
BACKGROUND Autosomal dominant spinocerebellar ataxia type 2 (SCA2) bears clinical and neuropathologic similarities to sporadic… (More)
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2004
2004
BACKGROUND We recently reported that spinocerebellar ataxia type 2 (SCA2) caused familial parkinsonism in 2 brothers with… (More)
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Highly Cited
2003
Highly Cited
2003
Cognitive impairment was studied in distinct types of spinocerebellar ataxia (SCA): eleven SCA1, 14 SCA2, and 11 SCA3 individuals… (More)
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Highly Cited
2000
Highly Cited
2000
OBJECTIVE To describe the clinical and molecular genetic analysis of a large family of northern Chinese descent with a mutation… (More)
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Highly Cited
1996
Highly Cited
1996
The gene for spinocerebellar ataxia type 2 (SCA2) has been mapped to 12q24.1. A1.1–megabase contig in the candidate region was… (More)
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Highly Cited
1996
Highly Cited
1996
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant, neurodegenerative disorder that affects the cerebellum and other… (More)
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Highly Cited
1996
Highly Cited
1996
Patients with spinocerebellar ataxia 3 (SCA3) and Machado-Joseph disease (MJD) carry an expanded CAG repeat in the MJD1 gene. One… (More)
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