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Showing articles 0 to 13 of 13 Filter Applied: Leigh's disease (Click to remove) Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Pyruvate Dehydrogenase Deficiency (PDCD) eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Leigh's Disease in an Adult with Evidence of"Inhibitor Factor"in Family Members Ann Neurol 3:519, Whetsell,W.O.,et al, 1978 Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease JAMA Neurol 73:668-674, Martikainen, M.H.,et al, 2016 Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease) Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014 A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia Neurol 72:1262-1276, DiMauro,S.,et al, 2009 Clinicopath Conf., Leighs syndrome, Intraventricular Hemorrhage and Periventricular Leukomalacia NEJM 359:1156-1166, Case 28-2008, 2008 Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities Ann Neurol 39:343-351, Rahman,S.,et al, 1996 Neurodegenerative Diseases of Childhood:MR and CT Evaluation J Comput Assist Tomogr 15:210-222, Mirowitz,S.A.,et al, 1991 Progressive Dystonia with Bilateral Putaminal Hypodensities Arch Neurol 44:1184-1187, Berkovic,S.F.,et al, 1987 Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 Encephalomyelopathy of Leigh Editorial BMJ 238, 1971, May., , 1971 Showing articles 0 to 13 of 13