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Nonfamilial Olivopontocerebellar Atrophy

Known as: Olivopontocerebellar Atrophy, Nonfamilial, Olivopontocerebellar Atrophies, Nonfamilial, Atrophy, Nonfamilial Olivopontocerebellar 
 
National Institutes of Health

Papers overview

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2016
2016
Objective:To identify susceptibility genes to nonfamilial hypokalemic periodic paralysis (hypoKPP) consisting of thyrotoxic… Expand
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2010
2010
The incidence of esophageal squamous cell carcinoma (ESCC) is very high in the northeast region of India. An earlier study from… Expand
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Highly Cited
2009
Highly Cited
2009
The vascular smooth muscle cell (SMC)-specific isoform of alpha-actin (ACTA2) is a major component of the contractile apparatus… Expand
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2008
2008
OBJECTIVE To test whether elevated hCG alone triggers spontaneous ovarian hyperstimulation syndrome (sOHSS). DESIGN… Expand
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2007
2007
Germline mutations in nuclear genes encoding mitochondrial enzymes fumarate hydratase (FH) and succinate dehydrogenase (subunits… Expand
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2003
2003
OBJECTIVE Cherubism is a rare hereditary multilocular cystic disease of the jaws, characterized by its typical appearance… Expand
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2002
2002
BACKGROUND Abnormalities in the prefrontal cortex have been implicated in the pathogenesis of major depressive disorder (MDD). To… Expand
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Highly Cited
1998
Highly Cited
1998
The cerebral cortex of Alzheimer's and Down syndrome patients is characterized by the presence of protein deposits in… Expand
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1994
1994
BACKGROUND Idiopathic dilated cardiomyopathy (DCM) is a serious heart disease characterized by enlargement of one or both… Expand
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1979
1979
Abstract Dextral, familial and nonfamilial sinistral Undergraduates, balanced by sex and all strongly dextral or sinistral… Expand
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