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Showing articles 0 to 10 of 10 Filter Applied: myopathy,mitochondrial (Click to remove) A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis Neurol 103:e209708, Wannarong,T.,et al, 2024 Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes) NEJM 376:1668-1678, CASE 13-2017, 2017 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Ophthalmologic Manifestations in MELAS Syndrome Arch Neurol 50:977-980, Fang,W.,et al, 1993 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation Neurol 42:545-550, Goto,Y.,et al, 1992 Mitochondrial Myopathy with a Defect of Mitochondrial-Protein Transport NEJM 323:37-42, Schapira,A.H.V.,et al, 1990 MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission Neurol 38:751-754, Montagne,P.,et al, 1988 Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study J Comput Assist Tomogr 12:854-857, DeVolder,A.,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