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Showing articles 0 to 11 of 11 Filter Applied: Leigh's disease (Click to remove) Pyruvate Dehydrogenase Deficiency (PDCD) eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018 Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities Ann Neurol 39:343-351, Rahman,S.,et al, 1996 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 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 Subacute Necrotizing Encephalopathy in Late Adolescence Arch Neurol 18:478, Hardman,J.M.,et al, 1968 Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus RadioGraphics 31:5-30, Hegde,A.N.,et al, 2011 Clinicopath Conf., Leighs syndrome, Intraventricular Hemorrhage and Periventricular Leukomalacia NEJM 359:1156-1166, Case 28-2008, 2008 Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome) Ann Neurol 6:200-206, Kalimo,H.,et al, 1979 Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem Neurol 23:1030, Sipe,J.C., 1973 Showing articles 0 to 11 of 11