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7. 3-Hydroxydicarboxylic and 3-ketodicarboxylic aciduria in three patients: evidence for a new defect in fatty acid oxidation at the level of 3-ketoacyl-CoA thiolase. Bennett MJ; Sherwood WG Clin Chem; 1993 May; 39(5):897-901. PubMed ID: 8485884 [TBL] [Abstract][Full Text] [Related]
14. 3-Hydroxydicarboxylic aciduria--a fatty acid oxidation defect with severe prognosis. Hagenfeldt L; von Döbeln U; Holme E; Alm J; Brandberg G; Enocksson E; Lindeberg L J Pediatr; 1990 Mar; 116(3):387-92. PubMed ID: 2308028 [TBL] [Abstract][Full Text] [Related]
15. Defects of mitochondrial beta-oxidation: a growing group of disorders. Vockley J; Whiteman DA Neuromuscul Disord; 2002 Mar; 12(3):235-46. PubMed ID: 11801395 [TBL] [Abstract][Full Text] [Related]
16. The diagnosis and biochemical investigation of a patient with a short chain fatty acid oxidation defect. Bennett MJ; Gray RG; Isherwood DM; Murphy N; Pollitt RJ J Inherit Metab Dis; 1985; 8 Suppl 2():135-6. PubMed ID: 3930866 [No Abstract] [Full Text] [Related]
17. Oxidation of fatty acids in cultured fibroblasts: a model system for the detection and study of defects in oxidation. Saudubray JM; Coudé FX; Demaugre F; Johnson C; Gibson KM; Nyhan WL Pediatr Res; 1982 Oct; 16(10):877-81. PubMed ID: 7145511 [TBL] [Abstract][Full Text] [Related]
18. Fatty acid mitochondrial beta-oxidation and hypoglycaemia in children. Taroni F; Uziel G Curr Opin Neurol; 1996 Dec; 9(6):477-85. PubMed ID: 9007409 [TBL] [Abstract][Full Text] [Related]
19. Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake. Stanley CA; DeLeeuw S; Coates PM; Vianey-Liaud C; Divry P; Bonnefont JP; Saudubray JM; Haymond M; Trefz FK; Breningstall GN Ann Neurol; 1991 Nov; 30(5):709-16. PubMed ID: 1763895 [TBL] [Abstract][Full Text] [Related]
20. Diagnosis of mitochondrial fatty acid oxidation defects. Duran M; Bruinvis L; Ketting D; Dorland L Padiatr Padol; 1993; 28(1):19-25. PubMed ID: 8446424 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]