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 *

183 related articles for article (PubMed ID: 1962058)

  • 21. [Clinical protocols concerned with disorders of fatty acid beta oxidation].
    Kania M
    Przegl Lek; 1994; 51(1):25-8. PubMed ID: 8208992
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Excess lipid availability increases mitochondrial fatty acid oxidative capacity in muscle: evidence against a role for reduced fatty acid oxidation in lipid-induced insulin resistance in rodents.
    Turner N; Bruce CR; Beale SM; Hoehn KL; So T; Rolph MS; Cooney GJ
    Diabetes; 2007 Aug; 56(8):2085-92. PubMed ID: 17519422
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prenatal diagnosis of mitochondrial fatty acid oxidation defects.
    Nada MA; Vianey-Saban C; Roe CR; Ding JH; Mathieu M; Wappner RS; Bialer MG; McGlynn JA; Mandon G
    Prenat Diagn; 1996 Feb; 16(2):117-24. PubMed ID: 8650121
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Lactic acid acidosis with mitochondrial myopathy due to a pyruvate dehydrogenase deficiency].
    Sperl W; Maurer H; Dworschak E; Höpfel I; Hammerer I
    Padiatr Padol; 1985; 20(1):55-67. PubMed ID: 3919358
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mitochondrial myopathies.
    DiMauro S; Bonilla E; Zeviani M; Nakagawa M; DeVivo DC
    Ann Neurol; 1985 Jun; 17(6):521-38. PubMed ID: 3927817
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Fatty acid oxidation disorders: maternal health and neonatal outcomes.
    Rector RS; Ibdah JA
    Semin Fetal Neonatal Med; 2010 Jun; 15(3):122-8. PubMed ID: 19926542
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Regulation of mitochondrial fatty acid β-oxidation in human: what can we learn from inborn fatty acid β-oxidation deficiencies?
    Bastin J
    Biochimie; 2014 Jan; 96():113-20. PubMed ID: 23764392
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mitochondrial fatty acid oxidation disorders in Thai infants: a report of 3 cases.
    Wasant P; Matsumoto I; Naylor E; Liammongkolkul S
    J Med Assoc Thai; 2002 Aug; 85 Suppl 2():S710-9. PubMed ID: 12403251
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Influence of dietary fatty acid chain-length on metabolic tolerance in mouse models of inherited defects in mitochondrial fatty acid beta-oxidation.
    Schuler AM; Gower BA; Matern D; Rinaldo P; Wood PA
    Mol Genet Metab; 2004 Dec; 83(4):322-9. PubMed ID: 15589119
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mitochondrial fatty acid oxidation and acute fatty liver of pregnancy.
    Treem WR
    Semin Gastrointest Dis; 2002 Jan; 13(1):55-66. PubMed ID: 11944635
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Progressive infantile neurodegeneration caused by 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency: a novel inborn error of branched-chain fatty acid and isoleucine metabolism.
    Zschocke J; Ruiter JP; Brand J; Lindner M; Hoffmann GF; Wanders RJ; Mayatepek E
    Pediatr Res; 2000 Dec; 48(6):852-5. PubMed ID: 11102558
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Metabolic studies on normal and pyruvate dehydrogenase deficient cultured human fibroblasts.
    Borud O; Stroomme JH
    Scand J Clin Lab Invest; 1977 Sep; 37(5):419-23. PubMed ID: 412246
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Systemic deficiency of the first component of the pyruvate dehydrogenase complex.
    Kerr DS; Ho L; Berlin CM; Lanoue KF; Towfighi J; Hoppel CL; Lusk MM; Gondek CM; Patel MS
    Pediatr Res; 1987 Sep; 22(3):312-8. PubMed ID: 3116495
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. 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]  

  • 36. [A case of congenital lactic acidosis caused by deficiency of pyruvate dehydrogenase].
    Salti R; Galluzzi F; Liguri GF; Marianelli L; Zammarchi E; La Cauza C
    Minerva Pediatr; 1979 Nov; 31(21):1539-46. PubMed ID: 118331
    [No Abstract]   [Full Text] [Related]  

  • 37. The enzymes of mitochondrial fatty acid oxidation.
    Bennett MJ
    Clin Chim Acta; 1994 May; 226(2):211-24. PubMed ID: 7923814
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Inborn errors of mitochondrial fatty acid oxidation.
    Bennett MJ; Rinaldo P; Strauss AW
    Crit Rev Clin Lab Sci; 2000 Feb; 37(1):1-44. PubMed ID: 10737439
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Fatal lactic acidosis due to deficiency of E1 component of the pyruvate dehydrogenase complex.
    Birch-Machin MA; Shepherd IM; Solomon M; Yeaman SJ; Gardner-Medwin D; Sherratt HS; Lindsay JG; Aynsley-Green A; Turnbull DM
    J Inherit Metab Dis; 1988; 11(2):207-17. PubMed ID: 3139934
    [TBL] [Abstract][Full Text] [Related]  

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

    [Previous]   [Next]    [New Search]
    of 10.