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Showing articles 0 to 8 of 8 Filter Applied: myopathy,mitochondrial (Click to remove) Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes) NEJM 376:1668-1678, CASE 13-2017, 2017 A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis Neurol 103:e209708, Wannarong,T.,et al, 2024 Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation Neurol 42:545-550, Goto,Y.,et al, 1992 MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission Neurol 38:751-754, Montagne,P.,et al, 1988 Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988 Clinicopath Conf Kearns-Sayre Syndrome (Oculocraniosomatic Neuromuscular Disease with Mitochondrial Myopathy) , Case, 4-1,NEJM 317:493-501,1987., 1987 Showing articles 0 to 8 of 8