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Showing articles 0 to 10 of 10 Filter Applied: exercise intolerance (Click to remove) Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes) NEJM 376:1668-1678, CASE 13-2017, 2017 A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery Neurol 88:e185-e189, Vazquez do Campo, R.,et al, 2017 A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness Neurol 86:e190-e194, McIntosh, P. & Karam, C., 2016 Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA NEJM 341:1037-1044, 1077, Andreu,A.L.,et al, 1999 McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature JNNP 55:407-408, Felice,K.J.,et al, 1992 Heterogeneity of Coenzyme Q10 Deficiency Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012 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 Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency Neurol 44:461-466, Wilkinson,D.A.,et al, 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