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Nonfamilial Olivopontocerebellar Atrophy

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

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Olivopontocerebellar Atrophies

Papers overview

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2016
2016
Novel susceptibility gene for nonfamilial hypokalemic periodic paralysis
Objective:To identify susceptibility genes to nonfamilial hypokalemic periodic paralysis (hypoKPP) consisting of thyrotoxic… Expand
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2010
2010
Contribution of germ line BRCA2 sequence alterations to risk of familial esophageal cancer in a high-risk area of India.
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
Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease.
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
Does elevated human chorionic gonadotropin alone trigger spontaneous ovarian hyperstimulation syndrome?
OBJECTIVE To test whether elevated hCG alone triggers spontaneous ovarian hyperstimulation syndrome (sOHSS). DESIGN… Expand
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2007
2007
Increased HIF1 alpha in SDH and FH deficient tumors does not cause microsatellite instability.
Germline mutations in nuclear genes encoding mitochondrial enzymes fumarate hydratase (FH) and succinate dehydrogenase (subunits… Expand
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2003
2003
A missense mutation in the SH3BP2 gene on chromosome 4p16.3 found in a case of nonfamilial cherubism.
OBJECTIVE Cherubism is a rare hereditary multilocular cystic disease of the jaws, characterized by its typical appearance… Expand
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2002
2002
Prefrontal cortical volume in childhood-onset major depression: preliminary findings.
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
Frameshift mutants of beta amyloid precursor protein and ubiquitin-B in Alzheimer's and Down patients.
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
Circulating heart autoantibodies in familial as compared with nonfamilial idiopathic dilated cardiomyopathy.
BACKGROUND Idiopathic dilated cardiomyopathy (DCM) is a serious heart disease characterized by enlargement of one or both… Expand
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1979
1979
A word-naming deficit in nonfamilial sinistrals? Laterality effects of vocal responses to tachistoscopically presented letter strings
Abstract Dextral, familial and nonfamilial sinistral Undergraduates, balanced by sex and all strongly dextral or sinistral… Expand
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