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Showing articles 0 to 9 of 9 Filter Applied: Leigh's disease (Click to remove) Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities Ann Neurol 39:343-351, Rahman,S.,et al, 1996 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 A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia Neurol 72:1262-1276, DiMauro,S.,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 Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome) Ann Neurol 6:200-206, Kalimo,H.,et al, 1979 Showing articles 0 to 9 of 9