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Showing articles 0 to 10 of 10 Filter Applied: exercise intolerance (Click to remove) Mitochondrial DNA Polymerase-y and Human Disease Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006 Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998 NEJM 339:1914-1923, , 1998 Heterogeneity of Coenzyme Q10 Deficiency Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012 MELAS MedLink.com, August, Klopstock, T., 2012 Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes) NEJM 376:1668-1678, CASE 13-2017, 2017 A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness Neurol 86:e190-e194, McIntosh, P. & Karam, C., 2016 Mitochondrial Respiratory-Chain Diseases NEJM 348:2656-2668, DiMauro,S. &Schon,E.A., 2003 Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation JNNP 69: 5-12, Gray,R.G.F. et al, 2000 Pseudoneurogenic Thoracic Outlet Syndrome Muscle & Nerve 17:242-244, Simpson,D.M., 1994 Phosphorylase Deficiency In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986 Showing articles 0 to 10 of 10