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Showing articles 0 to 12 of 12 Filter Applied: Leigh's disease (Click to remove) Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities Ann Neurol 39:343-351, Rahman,S.,et al, 1996 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 Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus RadioGraphics 31:5-30, Hegde,A.N.,et al, 2011 Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009 Bilateral Thalamic Lesions AJR 192:W53-W62, Smith,A.B.,et al, 2009 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 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 Subacute Necrotizing Encephalopathy in Late Adolescence Arch Neurol 18:478, Hardman,J.M.,et al, 1968 Showing articles 0 to 12 of 12