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Showing articles 0 to 10 of 10 Filter Applied: myopathy,mitochondrial (Click to remove) Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Mitochondrial Respiratory-Chain Diseases NEJM 348:2656-2668, DiMauro,S. &Schon,E.A., 2003 Mitochondrial DNA and Genetic Disease Editorial, Lancet 1:250-2511989., , 1989 Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 A 67-Year-Old Man with Exercise Intolerance nd Progressive Weakness Neurol 106:e214830, Gosset,A.,et al, 2026 Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009 Ophthalmologic Manifestations in MELAS Syndrome Arch Neurol 50:977-980, Fang,W.,et al, 1993 MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission Neurol 38:751-754, Montagne,P.,et al, 1988 MELAS Syndrome Involving a Mother & Two Children Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984 Showing articles 0 to 10 of 10