Variable Retinal and Neurologic Manifestations in Patients Harboring the Mitochondrial DNA 8993 Mutation
- 1 November 1993
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Ophthalmology (1950)
- Vol. 111 (11) , 1525-1530
- https://doi.org/10.1001/archopht.1993.01090110091031
Abstract
Research from JAMA Ophthalmology — Variable Retinal and Neurologic Manifestations in Patients Harboring the Mitochondrial DNA 8993 MutationKeywords
This publication has 14 references indexed in Scilit:
- A familial syndrome of dystonia, blepharospasm, and pigmentary retinopathyNeurology, 1990
- Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsiesBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1990
- Findings in muscle in complex I (NADH coenzyme Q reductase) deficiencyAnnals of Neurology, 1988
- Familial mitochondrial encephalomyopathy (MERRF): Genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA diseaseCell, 1988
- Mitochondrial myopathiesJournal of Inherited Metabolic Disease, 1987
- THE CLINICAL FEATURES OF MITOCHONDRIAL MYOPATHYBrain, 1986
- The Retinal Manifestations of Mitochondrial MyopathyArchives of Ophthalmology (1950), 1985
- Mitochondrial myopathiesAnnals of Neurology, 1985
- PIGMENT CHANGES OF THE RETINA IN CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA (CPEO)Acta Ophthalmologica, 1978
- Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart BlockA.M.A. Archives of Ophthalmology, 1958