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Showing articles 0 to 10 of 10 Filter Applied: mitochondrial disease (Click to remove) Pyruvate Dehydrogenase Deficiency (PDCD) eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018 Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes) NEJM 376:1668-1678, CASE 13-2017, 2017 Heterogeneity of Coenzyme Q10 Deficiency Arch Neurol 69:978-983, Emmanuele, V.,et al, 2012 MELAS MedLink.com, August, Klopstock, T., 2012 Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009 Acute Leukoencephalopathies:Differential Diagnosis and Investigation The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998 Parkinson's Disease NEJM 339:1044-1053,1130-1143, Lang,A.E.&Lozano,A.M., 1998 Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities Ann Neurol 39:343-351, Rahman,S.,et al, 1996 Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988 Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 Showing articles 0 to 10 of 10