Nonfamilial Olivopontocerebellar Atrophy

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

Topic mentions per year

Topic mentions per year

1966-2016
012319662016

Papers overview

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2009
2009
OBJECTIVES The objective of this study was to investigate functional effects of immunoadsorption (IA) in severely limited study… (More)
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2007
2007
Germline mutations in nuclear genes encoding mitochondrial enzymes fumarate hydratase (FH) and succinate dehydrogenase (subunits… (More)
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2006
2006
BACKGROUND Prior pilot investigation identified a larger pituitary gland volume (PGV) in pediatric patients with major depressive… (More)
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2003
2003
OBJECTIVE Cherubism is a rare hereditary multilocular cystic disease of the jaws, characterized by its typical appearance… (More)
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2002
2002
BACKGROUND Abnormalities in the prefrontal cortex have been implicated in the pathogenesis of major depressive disorder (MDD). To… (More)
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2002
2002
The change in QT interval with age during childhood of normal children and children with long QT syndrome (LQTS) and the effects… (More)
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1998
1998
Hypophosphatemic rickets is commonly an X-linked dominant disorder (XLH or HYP) associated with a renal tubular defect in… (More)
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1998
1998
BACKGROUND Although several genes or genetic loci that are responsible for or confer susceptibility to familial dilated… (More)
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1997
1997
Although several genes or genetic loci that are either responsible for or confer susceptibility to familial hypertrophic… (More)
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1984
1984
Twenty -six adrenal pheochromocytomas and four normal adrenal medullae were studied immunohistochemically. These included four… (More)
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