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Showing articles 0 to 14 of 14 Filter Applied: Leigh's disease (Click to remove) Leigh's Disease in an Adult with Evidence of"Inhibitor Factor"in Family Members Ann Neurol 3:519, Whetsell,W.O.,et al, 1978 Encephalomyelopathy of Leigh Editorial BMJ 238, 1971, May., , 1971 Pediatric Leigh Syndrome Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020 Pyruvate Dehydrogenase Deficiency (PDCD) eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018 Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus AJNR 38:1467-1474, Bond, K.M.,et al, 2017 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 The Use of Neuroimaging in the Diagnosis of Mitochondrial Disease Dev Disabil Res Rev 16:129-135, Friedman, S.D.,et al, 2010 The Incidence of Mitochondrial Encephalomyopathies in Childhood: Clinical Features and Morphological, Biochemical, and DNA Abnormalities Ann Neurol 49:377-383, Darin,N.,et al, 2001 Leigh Syndrome: Serial MR Imaging and Clinical Follow-Up AJNR 21:1502-1509, Arii,J. & Tanabe,Y., 2000 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 MR Findings in Patients with Subacute Necrotizing Encephalomyelopathy (Leigh Syndrome) AJR 154:1269-1274, Medina,L.,et al, 1990 Cytochrome c Oxidase Deficiency in Leigh Syndrome Ann Neurol 22:498-506, DiMauro,S.,et al, 1987 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 14 of 14