The Syndrome of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes Presenting Without Stroke

A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies

1990 • 2,006 citations

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1988 • 1,806 citations

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNALys mutation

1990 • 1,456 citations

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

1984 • 1,160 citations

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome

1989 • 1,009 citations

THE CLINICAL FEATURES OF MITOCHONDRIAL MYOPATHY

1986 • 418 citations

A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)

1990 • 361 citations

Mitochondrial myopathies: Clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA

1989 • 303 citations

MELAS syndrome

1988 • 179 citations

Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency

1988 • 101 citations

Clinical syndromes associated with ragged red fibers.

1991 • 74 citations

Mitochondrial myopathy and lactic acidaemia with myoclonic epilepsy, ataxia and hypothalamic infertility: a variant of Ramsay-Hunt syndrome?

1981 • 46 citations

Heterogeneous phenotypes of mitochondrial encephalomyopathy in a single kindred

1987 • 21 citations

Endocrine Aspects of Mitochondrial Cytopathy: Marked Phenotypic Variation in Two Affected Siblings

1990 • 2 citations