The mitochondrial encephalomyopathies are a diverse group of disorders that result from
the structural, biochemical, or genetic derangement of mitochondria. Since mitochondrial …

Twenty-five years of consumer socialization research have yielded an impressive set of
findings. The purpose of our article is to review these findings and assess what we know about …

Within the past 18 months, we have seen four cases of neurosyphilis at our institution (two
of meningovascular syphilis, one of acute syphilitic meningitis, and one of asymptomatic …

Albright's hereditary osteodystrophy is an autosomal dominant disorder characterized by a
short stature, brachydactyly, subcutaneous ossifications, and reduced expression or function …

A mitochondrial DNA mutation at nucleotide position 14,484 was found in 14 independent
probands with Leber hereditary optic neuropathy and in 0 250 controls. The 14,484 mutation, …

… Respiratory insufficiency or frank respiratory failure may rarely be the presenting or major
feature of a mitochondrial myopathy and may be due to depressed ventilatory drive in addition …

• Objective. —To define the clinical features of Leber's hereditary optic neuropathy associated
with the 14484 mitochondrial DNA mutation and to compare these features with those …

The objective of this study was to assess the effect of secukinumab, a monoclonal antibody
that inhibits interleukin (IL)-17A, on number of new active brain magnetic resonance imaging (…

… Dr Johns was supported by grant R 0 1 EY10864. ’lhis research was supporred in part by
a grant to Dr Beggs from the Knights Templar Foundation and a grant-in-aide in memory of …

Four unrelated patients presented with a severe sensory ataxic neuropathy in association
with dysarthria and chronic progressive external ophthalmoplegia. Electrophysiologic and …