Back to search

Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres

Data up to Jan 2025

Published1992
Citations62
References25

Total Citations Per Year

Abstract

References (25)

Adaptations of skeletal muscle to endurance exercise and their metabolic consequences

1984 • 1,940 citations

Muscle biopsy: A modern approach

1975 • 1,405 citations

Muscle Biopsy: A Modern Approach

1974 • 1,346 citations

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

1989 • 1,009 citations

NONDROPLET ULTRASTRUCTURAL DEMONSTRATION OF CYTOCHROME OXIDASE ACTIVITY WITH A POLYMERIZING OSMIOPHILIC REAGENT, DIAMINOBENZIDINE (DAB)

1968 • 892 citations

Deletions of mitochondrial DNA in Kearns‐Sayre syndrome

1988 • 730 citations

Deletions of mitochondrial DNA in Kearns‐Sayre syndrome

1988 • 354 citations

Lumping or splitting? “ophthalmoplegia‐plus” or kearns‐sayre syndrome?

1977 • 312 citations

Progressive Increase of the Mutated Mitochondrial DNA Fraction in Kearns-Sayre Syndrome

1990 • 311 citations

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

1989 • 303 citations

Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease

1990 • 248 citations

Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.

1989 • 212 citations

Leber's hereditary optic neuropathy and complex I deficiency in muscle

1991 • 161 citations

Widespread tissue distribution of mitochondrial DNA deletions in Kearns‐Sayre syndrome

1990 • 152 citations

Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesis.

1990 • 135 citations

Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations

1991 • 129 citations

Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies

1990 • 97 citations

cDNA Clone and Expression Analysis of Rodent Fast and Slow Skeletal Muscle Troponin I mRNAs

1989 • 82 citations

Mitochondria and muscular diseases

1982 • 73 citations

Immunocytochemical studies of cytochrome oxidase subunits in skeletal muscle of patients with partial cytochrome oxidase deficiencies

1988 • 52 citations

Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her child.

1992 • 50 citations

Replication-competent human mitochondrial DNA lacking the heavy-strand promoter region.

1991 • 46 citations

The molecular pathology of human respiratory chain defects.

1991 • 5 citations

The correlation between pathology, biochemistry and molecular genetics in mitochondrial encephalomyopathies

1991 • 3 citations

Molecular Basis of Neurological Disorders and Their Treatment

1991 • 3 citations

Cited By (0)

Loading...
Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres (1992) – Journal of the Neurological Sciences | Metascience Observatory Explorer