Nonfamilial Olivopontocerebellar Atrophy

OBJECTIVES The objective of this study was to investigate functional effects of immunoadsorption (IA) in severely limited study… (More)

Germline mutations in nuclear genes encoding mitochondrial enzymes fumarate hydratase (FH) and succinate dehydrogenase (subunits… (More)

BACKGROUND Prior pilot investigation identified a larger pituitary gland volume (PGV) in pediatric patients with major depressive… (More)

OBJECTIVE Cherubism is a rare hereditary multilocular cystic disease of the jaws, characterized by its typical appearance… (More)

BACKGROUND Abnormalities in the prefrontal cortex have been implicated in the pathogenesis of major depressive disorder (MDD). To… (More)

The change in QT interval with age during childhood of normal children and children with long QT syndrome (LQTS) and the effects… (More)

Hypophosphatemic rickets is commonly an X-linked dominant disorder (XLH or HYP) associated with a renal tubular defect in… (More)

BACKGROUND Although several genes or genetic loci that are responsible for or confer susceptibility to familial dilated… (More)

Although several genes or genetic loci that are either responsible for or confer susceptibility to familial hypertrophic… (More)

Twenty -six adrenal pheochromocytomas and four normal adrenal medullae were studied immunohistochemically. These included four… (More)