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Showing articles 0 to 10 of 10 Filter Applied: mitochondrial disease (Click to remove) Melas Syndrome Stat PearlsPubl Jan 25, Pia,S. & Lui,F., 2025 Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease JAMA Neurol 73:668-674, Martikainen, M.H.,et al, 2016 Wolff-Parkinson-White Syndrome in Patients with MELAS Arch Neurol 64:1625-1627, Sproule,D.M.,et al, 2007 Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene Brain 129:1674-1684, Horvath, R.,et al, 2006 Mitochondrial DNA Polymerase-y and Human Disease Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006 Mitochondrial Therapy for Parkinson Disease Arch Neurol 59:1523, Rosenberg,R.N., 2002 Parkinson's Disease NEJM 339:1044-1053,1130-1143, Lang,A.E.&Lozano,A.M., 1998 Generalized Mitochondrial Dysfunction in Parkinson's Disease Detected by Magnetic Resonance Spectroscopy of Muscle Neurol 45:2097-2099, Penn,A.M.W.,et al, 1995 Mitochondrial Involvement in Parkinson's Disease:The Controversy Continues Neurol 43:2170-2172, DiMauro,S., 1993 Mitochondrial Oxidative Phosphorylation Defects in Parkinson's Disease Ann Neurol 30:332-339, 3301991., Shoffner,J.M.,et al, 1991 Showing articles 0 to 10 of 10