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Showing articles 0 to 11 of 11 Filter Applied: Parkinson disease,etiology of (Click to remove) Update on Parkinson Disease NY State J Med, 87:147-1531987., Lieberman,A.N., 1987 Parkinson Disease Subtypes JAMA 71:499-504, Thenganatt, M. & Jankovic, J., 2014 Parkinson Disease, 10 Years After Its Genetic Revolution: Multiple Clues to a Complex Disorder Neurol 69:2093-2104, Klein,C. &Schlossmacher,M.G., 2007 Mitochondrial Therapy for Parkinson Disease Arch Neurol 59:1523, Rosenberg,R.N., 2002 Kindreds of Dominantly Inherited Parkinson's Disease:Keys to the Riddle Ann Neurol 38:355-356, Duvoisin,R.C.&Golbe,L.I., 1995 A Greek-American Kindred with Autosomal Dominant, Levodopa-Responsive Parkinsonism and Anticipation Ann Neurol 38:373-378, 3551995., Markopoulou,K.,et al, 1995 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 Increased Risk of Parkinson's Disease in Parents and Siblings of Patients Ann Neurol 36:659-661, Payami,H.,et al, 1994 Identical Twins with Similar Onset of Parkinson's Disease:A Case Report Neurol 43:1159-1161, Pahwa,R.,et al, 1993 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 11 of 11