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Spinocerebellar Ataxia Type 2

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

Papers overview

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Review
2017
Review
2017
INTRODUCTION Vulvar and vaginal atrophy (VVA) affects up to two thirds of postmenopausal women, but most symptomatic women do not… Expand
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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… Expand
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Highly Cited
2009
Highly Cited
2009
Although beta-amyloid (Abeta) plaques are a primary diagnostic criterion for Alzheimer's disease, this pathology is commonly… Expand
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Highly Cited
2007
Highly Cited
2007
Objective:To evaluate the utility of MRI hippocampal and entorhinal cortex atrophy in predicting conversion from mild cognitive… Expand
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Highly Cited
2004
Highly Cited
2004
MICA molecules interact with the NKG2D-activating receptor on human NK and CD8 T cells. We investigated the participation of the… Expand
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Highly Cited
2000
Highly Cited
2000
Studies at the basic and clinical levels demonstrate that neuronal atrophy and cell death occur in response to stress and in the… Expand
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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… Expand
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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… Expand
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Highly Cited
1995
Highly Cited
1995
A POLYGLUTAMINE expansion (encoded by a CAG repeat) in specific proteins causes neurodegeneration in Huntington's disease (HD… Expand
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Highly Cited
1993
Highly Cited
1993
The pathogenesis of reflex sympathetic dystrophy--variously known as Sudeck's atrophy, causalgia, algodystrophy, and peripheral… Expand
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