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Showing articles 0 to 9 of 9 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 Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999 Investigation of Muscle Disease JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996 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 Zidovudine Myopathy:A Distinctive Disorder Associated with Mitochondrial Dysfunction Ann Neurol 29:606-614, Mhiri,C.,et al, 1991 Mitochondrial Myopathy Caused by Long-Term Ziduvudine Therapy NEJM 322:1098-1105, Dalakas,M.C.,et al, 1990 MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission Neurol 38:751-754, Montagne,P.,et al, 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 9 of 9