184 related articles for article (PubMed ID: 12394635)
21. Strategies for the diagnosis of mitochondrial fatty acid beta-oxidation disorders.
Sim KG; Hammond J; Wilcken B
Clin Chim Acta; 2002 Sep; 323(1-2):37-58. PubMed ID: 12135806
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. Genetic disorders of carnitine metabolism and their nutritional management.
Kerner J; Hoppel C
Annu Rev Nutr; 1998; 18():179-206. PubMed ID: 9706223
[TBL] [Abstract][Full Text] [Related]
24. An introduction to nutritional treatment in inborn errors of metabolism--different disorders, different approaches.
Wilcken B
Southeast Asian J Trop Med Public Health; 2003; 34 Suppl 3():198-201. PubMed ID: 15906735
[TBL] [Abstract][Full Text] [Related]
25. [Mitochondrial beta-oxidation defects: overview].
Yamaguchi S
Ryoikibetsu Shokogun Shirizu; 2001; (36):60-4. PubMed ID: 11596451
[No Abstract] [Full Text] [Related]
26. Fatty Acid oxidation defects.
Goh DL
Ann Acad Med Singap; 2008 Dec; 37(12 Suppl):74-3. PubMed ID: 19904457
[TBL] [Abstract][Full Text] [Related]
27. Selective Screening of Fatty Acids Oxidation Defects and Organic Acidemias by Liquid Chromatography/tandem Mass Spectrometry Acylcarnitine Analysis in Brazilian Patients.
Vargas CR; Ribas GS; da Silva JM; Sitta A; Deon M; de Moura Coelho D; Wajner M
Arch Med Res; 2018 Apr; 49(3):205-212. PubMed ID: 30119976
[TBL] [Abstract][Full Text] [Related]
28. Fatty acid oxidation in peripheral blood cells: characterization and use for the diagnosis of defects of fatty acid oxidation.
Schaefer J; Pourfarzam M; Bartlett K; Jackson S; Turnbull DM
Pediatr Res; 1995 Mar; 37(3):354-60. PubMed ID: 7784145
[TBL] [Abstract][Full Text] [Related]
29. Defects in mitochondrial fatty acid oxidation: clinical presentations and their role in sudden infant death.
Pollitt RJ
Padiatr Padol; 1993; 28(1):13-7. PubMed ID: 8446423
[TBL] [Abstract][Full Text] [Related]
30. Inborn defects of fatty acid oxidation: a preventable cause of SIDS.
Keppen LD; Randall B
S D J Med; 1999 Jun; 52(6):187-8; disscussion 188-9. PubMed ID: 10388343
[TBL] [Abstract][Full Text] [Related]
31. Fifty years of research on mitochondrial fatty acid oxidation disorders: The remaining challenges.
Vianey-Saban C; Guffon N; Fouilhoux A; Acquaviva C
J Inherit Metab Dis; 2023 Sep; 46(5):848-873. PubMed ID: 37530674
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Nutritional management of infants with inborn metabolic errors.
Morrow G
Clin Perinatol; 1975 Sep; 2(2):361-72. PubMed ID: 1102228
[TBL] [Abstract][Full Text] [Related]
34. Long chain fatty acid oxidation defects in children: importance of detection and treatment options.
Hayes B; Lynch B; O'Keefe M; Monavari AA; Treacy EP
Ir J Med Sci; 2007 Sep; 176(3):189-92. PubMed ID: 17431731
[TBL] [Abstract][Full Text] [Related]
35. Analysis of fatty acid oxidation intermediates in cultured fibroblasts to detect mitochondrial oxidation disorders.
Pourfarzam M; Schaefer J; Turnbull DM; Bartlett K
Clin Chem; 1994 Dec; 40(12):2267-75. PubMed ID: 7988014
[TBL] [Abstract][Full Text] [Related]
36. Complications in early diagnosis and treatment of two infants with long-chain fatty acid beta-oxidation defects.
Skladal D; Sass JO; Geiger H; Geiger R; Mann C; Vreken P; Wanders RJ; Trawöger R
J Pediatr Gastroenterol Nutr; 2000 Oct; 31(4):448-52. PubMed ID: 11045847
[No Abstract] [Full Text] [Related]
37. Molecular basis of mitochondrial fatty acid oxidation defects.
Coates PM; Tanaka K
J Lipid Res; 1992 Aug; 33(8):1099-110. PubMed ID: 1431593
[TBL] [Abstract][Full Text] [Related]
38. [INBORN ERRORS OF FATTY ACID METABOLISM (REVIEW)].
Zharmakhanova G; Syrlybayeva L; Nurbaulina E; Baikadamova L; Eshtayeva G
Georgian Med News; 2020 Jun; (303):161-167. PubMed ID: 32841199
[TBL] [Abstract][Full Text] [Related]
39. Role of carnitine and fatty acid oxidation and its defects in infantile epilepsy.
Tein I
J Child Neurol; 2002 Dec; 17 Suppl 3():3S57-82; discussion 3S82-3. PubMed ID: 12597056
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
