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5. Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship. Gregersen N; Andresen BS; Corydon MJ; Corydon TJ; Olsen RK; Bolund L; Bross P Hum Mutat; 2001 Sep; 18(3):169-89. PubMed ID: 11524729 [TBL] [Abstract][Full Text] [Related]
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7. Inherited disorders of mitochondrial fatty acid oxidation. Coates PM; Stanley CA Prog Liver Dis; 1992; 10():123-38. PubMed ID: 1296227 [No Abstract] [Full Text] [Related]
8. The inborn errors of peroxisomal beta-oxidation: a review. Wanders RJ; van Roermund CW; Schutgens RB; Barth PG; Heymans HS; van den Bosch H; Tager JM J Inherit Metab Dis; 1990; 13(1):4-36. PubMed ID: 2109148 [TBL] [Abstract][Full Text] [Related]
9. Very long chain acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblasts. Bertrand C; Largillière C; Zabot MT; Mathieu M; Vianey-Saban C Biochim Biophys Acta; 1993 Jan; 1180(3):327-9. PubMed ID: 8422439 [TBL] [Abstract][Full Text] [Related]
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11. New genetic defects in mitochondrial fatty acid oxidation and carnitine deficiency. Stanley CA Adv Pediatr; 1987; 34():59-88. PubMed ID: 3318304 [TBL] [Abstract][Full Text] [Related]
12. Mitochondrial fatty acid beta-oxidation in the human eye and brain: implications for the retinopathy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Tyni T; Paetau A; Strauss AW; Middleton B; Kivelä T Pediatr Res; 2004 Nov; 56(5):744-50. PubMed ID: 15347768 [TBL] [Abstract][Full Text] [Related]
13. Mitochondrial dysfunction in fatty acid oxidation disorders: insights from human and animal studies. Wajner M; Amaral AU Biosci Rep; 2015 Nov; 36(1):e00281. PubMed ID: 26589966 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Disorders of mitochondrial fatty acyl-CoA beta-oxidation. Wanders RJ; Vreken P; den Boer ME; Wijburg FA; van Gennip AH; IJlst L J Inherit Metab Dis; 1999 Jun; 22(4):442-87. PubMed ID: 10407780 [TBL] [Abstract][Full Text] [Related]
17. Clinical and biochemical aspects of carnitine deficiency and insufficiency: transport defects and inborn errors of beta-oxidation. Angelini C; Vergani L; Martinuzzi A Crit Rev Clin Lab Sci; 1992; 29(3-4):217-42. PubMed ID: 1489518 [TBL] [Abstract][Full Text] [Related]
18. Fatty acid beta-oxidation in leukocytes from control subjects and medium-chain acyl-CoA dehydrogenase deficient patients. Wanders RJ; Ijlst L Biochim Biophys Acta; 1992 Jan; 1138(1):80-4. PubMed ID: 1737072 [TBL] [Abstract][Full Text] [Related]
19. Heat stress deteriorates mitochondrial beta-oxidation of long-chain fatty acids in cultured fibroblasts with fatty acid beta-oxidation disorders. Li H; Fukuda S; Hasegawa Y; Purevsuren J; Kobayashi H; Mushimoto Y; Yamaguchi S J Chromatogr B Analyt Technol Biomed Life Sci; 2010 Jun; 878(20):1669-72. PubMed ID: 20207594 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]