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Journal Abstract Search

113 related items for PubMed ID: 9590085

  • 21. Acyl-CoA dehydrogenase 9 (ACAD 9) is the long-chain acyl-CoA dehydrogenase in human embryonic and fetal brain.
    Oey NA, Ruiter JP, Ijlst L, Attie-Bitach T, Vekemans M, Wanders RJ, Wijburg FA.
    Biochem Biophys Res Commun; 2006 Jul 21; 346(1):33-7. PubMed ID: 16750164
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  • 22. Commentary on a Delphi clinical practice protocol for the diagnosis and management of very long chain acyl-CoA dehydrogenase deficiency by Arnold et al.
    Marsden DL.
    Mol Genet Metab; 2009 Mar 21; 96(3):81-2. PubMed ID: 19081279
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  • 23. Reye syndrome and reye-like syndrome.
    Gosalakkal JA, Kamoji V.
    Pediatr Neurol; 2008 Sep 21; 39(3):198-200. PubMed ID: 18725066
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  • 24. [Acyl-CoA dehydrogenase deficiency (very-long-chain, long-chain, medium-chain, short-chain), mitochondrial].
    Yamaguchi S.
    Ryoikibetsu Shokogun Shirizu; 2001 Sep 21; (33):144-7. PubMed ID: 11462373
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  • 26. [Very-long-chain acyl-CoA dehydrogenase deficiency].
    Uchiyama A, Takusa Y, Yamaguchi S.
    Ryoikibetsu Shokogun Shirizu; 2001 Sep 21; (36):65-7. PubMed ID: 11596452
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  • 30. 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 21; 83(4):322-9. PubMed ID: 15589119
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  • 32. Perioperative measures in very long chain acyl-CoA dehydrogenase deficiency.
    Vellekoop P, Diekman EF, van Tuijl I, de Vries MM, van Hasselt PM, Visser G.
    Mol Genet Metab; 2011 May 21; 103(1):96-7. PubMed ID: 21333574
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  • 33. Intermittent rhabdomyolysis with adult onset associated with a mutation in the ACADVL gene.
    Antunes AP, Nogueira C, Rocha H, Vilarinho L, Evangelista T.
    J Clin Neuromuscul Dis; 2013 Dec 21; 15(2):69-72. PubMed ID: 24263034
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  • 35. A simple spectrophotometric assay for long-chain acyl-CoA dehydrogenase activity measurements in human skin fibroblasts.
    Ijlst L, Wanders RJ.
    Ann Clin Biochem; 1993 May 21; 30 ( Pt 3)():293-7. PubMed ID: 8517612
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  • 36. Breath-holding spell and macrocytic anaemia in a toddler.
    Ramachandran S, Alessandri A, Price J, Balasubramaniam S.
    Br J Haematol; 2014 Jul 21; 166(2):156. PubMed ID: 24797152
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  • 37. Very long-chain acyl coenzyme A dehydrogenase deficiency presenting with exercise-induced myoglobinuria.
    Ogilvie I, Pourfarzam M, Jackson S, Stockdale C, Bartlett K, Turnbull DM.
    Neurology; 1994 Mar 21; 44(3 Pt 1):467-73. PubMed ID: 8145917
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  • 38. Screening of the most common medium-chain acyl CoA dehydrogenase (MCAD) deficiency mutation (K329E) in the Czech newborn population.
    Kozàk L, Hrabincovà E, Rudolfoà J, Vràbelovà S, Freiberger T.
    Southeast Asian J Trop Med Public Health; 1999 Mar 21; 30 Suppl 2():49-50. PubMed ID: 11400780
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