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Showing articles 0 to 8 of 8 Filter Applied: myopathy,mitochondrial (Click to remove) Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes) NEJM 376:1668-1678, CASE 13-2017, 2017 Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder Neurol 44:721-727, Hirano,M.,et al, 1994 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) :Clin Features & DNA Mutation Neurol 42:545-550, Goto,Y.,et al, 1992 Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992 Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA Ann Neurol 26:699-708, Hold,I.J.,et al, 1989 MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission Neurol 38:751-754, Montagne,P.,et al, 1988 Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 Showing articles 0 to 8 of 8