These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

81 related articles for article (PubMed ID: 12014007)

  • 21. Defects of fatty acid oxidation in skeletal muscle.
    Turnbull DM; Bartlett K; Watmough NJ; Shepherd IM; Sherratt HS
    J Inherit Metab Dis; 1987; 10 Suppl 1():105-12. PubMed ID: 3119934
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Bezafibrate increases very-long-chain acyl-CoA dehydrogenase protein and mRNA expression in deficient fibroblasts and is a potential therapy for fatty acid oxidation disorders.
    Djouadi F; Aubey F; Schlemmer D; Ruiter JP; Wanders RJ; Strauss AW; Bastin J
    Hum Mol Genet; 2005 Sep; 14(18):2695-703. PubMed ID: 16115821
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Inherited defects of mitochondrial fatty acid oxidation.
    Turnbull DM; Shepherd IM; Aynsley-Green A
    Biochem Soc Trans; 1988 Jun; 16(3):424-7. PubMed ID: 3181618
    [No Abstract]   [Full Text] [Related]  

  • 24. Medium chain acyl-coenzyme A dehydrogenase deficiency.
    Bennett MJ; Hale DE
    N J Med; 1992 Sep; 89(9):675-8. PubMed ID: 1436730
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. [Metabolic crisis in an infant--is the problem in the mitochondria?].
    Tyni T; Pihko H
    Duodecim; 2002; 118(13):1331-9. PubMed ID: 12239878
    [No Abstract]   [Full Text] [Related]  

  • 28. Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency.
    Duran M; Hofkamp M; Rhead WJ; Saudubray JM; Wadman SK
    Pediatrics; 1986 Dec; 78(6):1052-7. PubMed ID: 3786030
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Mitochondrial trifunctional protein].
    Uchiyama A; Yamaguchi S
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():109-12. PubMed ID: 12013829
    [No Abstract]   [Full Text] [Related]  

  • 30. Clinical diagnosis of long-chain acyl-coenzyme A-dehydrogenase deficiency: use of stress and fat-loading tests.
    Parini R; Garavaglia B; Saudubray JM; Bardelli P; Melotti D; Zecca G; Di Donato S
    J Pediatr; 1991 Jul; 119(1 Pt 1):77-80. PubMed ID: 2066862
    [No Abstract]   [Full Text] [Related]  

  • 31. Cloning of human very-long-chain acyl-coenzyme A dehydrogenase and molecular characterization of its deficiency in two patients.
    Aoyama T; Souri M; Ueno I; Kamijo T; Yamaguchi S; Rhead WJ; Tanaka K; Hashimoto T
    Am J Hum Genet; 1995 Aug; 57(2):273-83. PubMed ID: 7668252
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Methods for the investigation of hypoglycaemia with particular reference to inherited disorders of mitochondrial beta-oxidation.
    Bartlett K
    Baillieres Clin Endocrinol Metab; 1993 Jul; 7(3):643-67. PubMed ID: 8379909
    [No Abstract]   [Full Text] [Related]  

  • 33. Very-long-chain acyl-coenzyme A dehydrogenase (VLCAD) deficiency: monitoring of treatment by carnitine/acylcarnitine analysis in blood spots.
    Spiekerkötter U; Schwahn B; Korall H; Trefz FK; Andresen BS; Wendel U
    Acta Paediatr; 2000 Apr; 89(4):492-5. PubMed ID: 10830467
    [No Abstract]   [Full Text] [Related]  

  • 34. The frequency of MCAD mutation (K329E) in the Finnish population.
    Schwartz EI; Ilonen J; Skobeleva NA; Akerblom HK
    Eur J Pediatr; 1995 Jun; 154(6):501. PubMed ID: 7671954
    [No Abstract]   [Full Text] [Related]  

  • 35. [Enzymes of mitochondrial beta-oxidation].
    Yamaguchi S
    Nihon Rinsho; 2002 Apr; 60 Suppl 4():88-93. PubMed ID: 12014005
    [No Abstract]   [Full Text] [Related]  

  • 36. Inborn errors of mitochondrial acyl-coenzyme a metabolism: acyl-CoA biology meets the clinic.
    Yang H; Zhao C; Tang MC; Wang Y; Wang SP; Allard P; Furtos A; Mitchell GA
    Mol Genet Metab; 2019; 128(1-2):30-44. PubMed ID: 31186158
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Diagnostic tests for acyl-coenzyme A dehydrogenase deficiency.
    Elpeleg ON
    J Pediatr; 1992 Oct; 121(4):667-8. PubMed ID: 1403411
    [No Abstract]   [Full Text] [Related]  

  • 38. Mitochondrial myopathies: defects in beta-oxidation.
    Turnbull DM; Sherratt HS
    Biochem Soc Trans; 1985 Aug; 13(4):645-7. PubMed ID: 3161765
    [No Abstract]   [Full Text] [Related]  

  • 39. Defects in mitochondrial beta-oxidation of fatty acids.
    Wood PA
    Curr Opin Lipidol; 1999 Apr; 10(2):107-12. PubMed ID: 10327278
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Fatty acid metabolism in mitochondria: defects and genetics.
    Coates PM
    Biofactors; 1998; 7(3):201-2. PubMed ID: 9568246
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.