BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 9932958)

  • 21. An acyl-coenzyme A dehydrogenase assay utilizing the ferricenium ion.
    Lehman TC; Hale DE; Bhala A; Thorpe C
    Anal Biochem; 1990 May; 186(2):280-4. PubMed ID: 2363500
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Medium chain acyl-CoA dehydrogenase deficiency. Apropos of a case with demonstration of this enzyme deficiency].
    Collet JP; Divry P; Blanc JF; Guibaud P; David M; Macabeo V; Vibert J; Hermier M
    Pediatrie; 1984 Dec; 39(8):661-8. PubMed ID: 6535973
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A case report of short-chain acyl-CoA dehydrogenase deficiency (SCADD).
    Lampret BR; Murko S; Debeljak M; Tansek MZ; Fister P; Battelino T
    Biochem Med (Zagreb); 2015; 25(2):279-84. PubMed ID: 26110041
    [TBL] [Abstract][Full Text] [Related]  

  • 24. ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.
    Olsen RK; Olpin SE; Andresen BS; Miedzybrodzka ZH; Pourfarzam M; Merinero B; Frerman FE; Beresford MW; Dean JC; Cornelius N; Andersen O; Oldfors A; Holme E; Gregersen N; Turnbull DM; Morris AA
    Brain; 2007 Aug; 130(Pt 8):2045-54. PubMed ID: 17584774
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Perioperative management of a child with short-chain acyl-CoA dehydrogenase deficiency.
    Turpin B; Tobias JD
    Paediatr Anaesth; 2005 Sep; 15(9):771-7. PubMed ID: 16101709
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Hydroxylated Long-Chain Acylcarnitines are Biomarkers of Mitochondrial Myopathy.
    Vissing CR; Dunø M; Wibrand F; Christensen M; Vissing J
    J Clin Endocrinol Metab; 2019 Dec; 104(12):5968-5976. PubMed ID: 31294795
    [TBL] [Abstract][Full Text] [Related]  

  • 27. An unusually high frequency of SCAD deficiency caused by two pathogenic variants in the ACADS gene and its relationship to the ethnic structure in Slovakia.
    Lisyová J; Chandoga J; Jungová P; Repiský M; Knapková M; Machková M; Dluholucký S; Behúlová D; Šaligová J; Potočňáková Ľ; Lysinová M; Böhmer D
    BMC Med Genet; 2018 Apr; 19(1):64. PubMed ID: 29678161
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Rhabdomyolysis and acute encephalopathy in late onset medium chain acyl-CoA dehydrogenase deficiency.
    Ruitenbeek W; Poels PJ; Turnbull DM; Garavaglia B; Chalmers RA; Taylor RW; Gabreëls FJ
    J Neurol Neurosurg Psychiatry; 1995 Feb; 58(2):209-14. PubMed ID: 7876853
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency.
    Corydon MJ; Vockley J; Rinaldo P; Rhead WJ; Kjeldsen M; Winter V; Riggs C; Babovic-Vuksanovic D; Smeitink J; De Jong J; Levy H; Sewell AC; Roe C; Matern D; Dasouki M; Gregersen N
    Pediatr Res; 2001 Jan; 49(1):18-23. PubMed ID: 11134486
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Multiple acyl-CoA dehydrogenase deficiency (MADD): a curable cause of genetic muscular lipidosis].
    Maillart E; Acquaviva-Bourdain C; Rigal O; Brivet M; Jardel C; Lombès A; Eymard B; Vianey-Saban C; Laforêt P
    Rev Neurol (Paris); 2010 Mar; 166(3):289-94. PubMed ID: 19592060
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Rapid degradation of short-chain acyl-CoA dehydrogenase variants with temperature-sensitive folding defects occurs after import into mitochondria.
    Corydon TJ; Bross P; Jensen TG; Corydon MJ; Lund TB; Jensen UB; Kim JJ; Gregersen N; Bolund L
    J Biol Chem; 1998 May; 273(21):13065-71. PubMed ID: 9582344
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein.
    Goodman SI; McCabe ER; Fennessey PV; Mace JW
    Pediatr Res; 1980 Jan; 14(1):12-7. PubMed ID: 7360517
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Assay of acyl-CoA dehydrogenases in muscle and liver and identification of four new cases of medium-chain acyl-CoA dehydrogenase deficiency associated with systemic carnitine deficiency.
    Zierz S; Engel AG; Romshe CA
    Adv Neurol; 1988; 48():231-7. PubMed ID: 3334785
    [No Abstract]   [Full Text] [Related]  

  • 34. Decompensation of hepatic and cerebral acyl-CoA metabolism in BALB/cByJ mice by chronic riboflavin deficiency: restoration by acetyl-L-carnitine.
    Rao KV; Qureshi IA
    Can J Physiol Pharmacol; 1997 May; 75(5):423-30. PubMed ID: 9250376
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency.
    Pourfarzam M; Morris A; Appleton M; Craft A; Bartlett K
    Lancet; 2001 Sep; 358(9287):1063-4. PubMed ID: 11589939
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Acylcarnitine removal in a patient with acyl-CoA beta-oxidation deficiency disorder: effect of L-carnitine therapy and starvation.
    Fontaine M; Briand G; Vallée L; Ricart G; Degand P; Divry P; Vianey-Saban C; Vamecq J
    Clin Chim Acta; 1996 Aug; 252(2):109-22. PubMed ID: 8853559
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Evaluation of newborn screening for medium chain acyl-CoA dehydrogenase deficiency in 275 000 babies.
    Carpenter K; Wiley V; Sim KG; Heath D; Wilcken B
    Arch Dis Child Fetal Neonatal Ed; 2001 Sep; 85(2):F105-9. PubMed ID: 11517203
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Short-chain acyl-coenzyme A dehydrogenase deficiency in mice.
    Wood PA; Amendt BA; Rhead WJ; Millington DS; Inoue F; Armstrong D
    Pediatr Res; 1989 Jan; 25(1):38-43. PubMed ID: 2919115
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Characterization of two ETFDH mutations in a novel case of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
    Missaglia S; Tavian D; Moro L; Angelini C
    Lipids Health Dis; 2018 Nov; 17(1):254. PubMed ID: 30424791
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 9.