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9. Defective activation of the pyruvate dehydrogenase complex in subacute necrotizing encephalomyelopathy (Leigh disease). DeVivo DC; Haymond MW; Obert KA; Nelson JS; Pagliara AS Ann Neurol; 1979 Dec; 6(6):483-94. PubMed ID: 119480 [TBL] [Abstract][Full Text] [Related]
10. Outcome of thiamine treatment in a child with Leigh disease due to thiamine-responsive pyruvate dehydrogenase deficiency. Di Rocco M; Lamba LD; Minniti G; Caruso U; Naito E Eur J Paediatr Neurol; 2000; 4(3):115-7. PubMed ID: 10872106 [TBL] [Abstract][Full Text] [Related]
12. [Leigh's encephalomyelopathy and its related diseases]. Narisawa K No To Shinkei; 1985 Nov; 37(11):1108-9. PubMed ID: 3935145 [No Abstract] [Full Text] [Related]
13. [Subacute necrotizing encephalopathy, Leigh's disease. Apropos of a case]. Delisle MB; Netter JC; Peyrille F; Bouissou H Ann Pathol; 1985; 5(4-5):313-7. PubMed ID: 3833250 [TBL] [Abstract][Full Text] [Related]
14. [Leigh's syndrome and mitochondrial myopathy]. Nakase H Nihon Rinsho; 1993 Sep; 51(9):2403-8. PubMed ID: 8411720 [TBL] [Abstract][Full Text] [Related]
15. Pyruvate dehydrogenase activity is not deficient in the brain of three autopsied cases with Leigh disease (subacute necrotizing encephalomyelopathy, SNE). Kustermann-Kuhn B; Harzer K; Schröder R; Permanetter W; Peiffer J Hum Genet; 1984; 68(1):51-3. PubMed ID: 6437963 [TBL] [Abstract][Full Text] [Related]
16. Leigh syndrome: pyruvate dehydrogenase defect. A case with peripheral neuropathy. Chabrol B; Mancini J; Benelli C; Gire C; Munnich A J Child Neurol; 1994 Jan; 9(1):52-5. PubMed ID: 8151084 [TBL] [Abstract][Full Text] [Related]
17. MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh syndrome): correlation with biochemical defect. Medina L; Chi TL; DeVivo DC; Hilal SK AJNR Am J Neuroradiol; 1990; 11(2):379-84. PubMed ID: 2156413 [TBL] [Abstract][Full Text] [Related]
18. Spectrum of neurological and survival outcomes in pyruvate dehydrogenase complex (PDC) deficiency: lack of correlation with genotype. DeBrosse SD; Okajima K; Zhang S; Nakouzi G; Schmotzer CL; Lusk-Kopp M; Frohnapfel MB; Grahame G; Kerr DS Mol Genet Metab; 2012 Nov; 107(3):394-402. PubMed ID: 23021068 [TBL] [Abstract][Full Text] [Related]
19. Biotinidase deficiency: a cause of subacute necrotizing encephalomyelopathy (Leigh syndrome). Report of a case with lethal outcome. Baumgartner ER; Suormala TM; Wick H; Probst A; Blauenstein U; Bachmann C; Vest M Pediatr Res; 1989 Sep; 26(3):260-6. PubMed ID: 2587127 [TBL] [Abstract][Full Text] [Related]
20. Deficiency of respiratory chain complex I is a common cause of Leigh disease. Morris AA; Leonard JV; Brown GK; Bidouki SK; Bindoff LA; Woodward CE; Harding AE; Lake BD; Harding BN; Farrell MA; Bell JE; Mirakhur M; Turnbull DM Ann Neurol; 1996 Jul; 40(1):25-30. PubMed ID: 8687187 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]