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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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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
2003
2003
OBJECTIVE Cherubism is a rare hereditary multilocular cystic disease of the jaws, characterized by its typical appearance… Expand
Highly Cited
2002
Highly Cited
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
1994
1994
BACKGROUND Idiopathic dilated cardiomyopathy (DCM) is a serious heart disease characterized by enlargement of one or both… Expand
1987
1987
To the Editor.— The results presented in the article entitled "Therapeutic Response to Lovastatin (Mevinolin) in Nonfamilial… Expand
1985
1985
High affinity 3H-imipramine binding sites have been demonstrated in human brain and platelet membranes. It has been suggested… Expand
Highly Cited
1979
Highly Cited
1979
Abstract Dextral, familial and nonfamilial sinistral Undergraduates, balanced by sex and all strongly dextral or sinistral… Expand