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Journal Abstract Search

555 related items for PubMed ID: 18725066

  • 1. Reye syndrome and reye-like syndrome.
    Gosalakkal JA, Kamoji V.
    Pediatr Neurol; 2008 Sep; 39(3):198-200. PubMed ID: 18725066
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  • 2. [Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in 2 patients with symptoms of Reye syndrome].
    Brus F, Smit GP, Knoester H, Reijngoud DJ.
    Tijdschr Kindergeneeskd; 1988 Jun; 56(3):132-7. PubMed ID: 3046055
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  • 3. 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
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  • 6. Medium-chain acyl CoA dehydrogenase deficiency: electron microscopic differentiation from Reye syndrome.
    Santer R, Schmidt-Sommerfeld E, Leung YK, Fischer JE, Lebenthal E.
    Eur J Pediatr; 1990 Dec; 150(2):111-4. PubMed ID: 2279505
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  • 7. 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
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  • 9. Is autism a disorder of fatty acid metabolism? Possible dysfunction of mitochondrial beta-oxidation by long chain acyl-CoA dehydrogenase.
    Clark-Taylor T, Clark-Taylor BE.
    Med Hypotheses; 2004 Dec; 62(6):970-5. PubMed ID: 15142659
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  • 13. Medium-chain acyl-CoA dehydrogenase deficiency.
    Egidio RJ, Francis GL, Coates PM, Hale DE, Roesel A.
    Am Fam Physician; 1989 May; 39(5):221-6. PubMed ID: 2718899
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  • 14. Relationship between unusual hepatic acyl coenzyme A profiles and the pathogenesis of Reye syndrome.
    Corkey BE, Hale DE, Glennon MC, Kelley RI, Coates PM, Kilpatrick L, Stanley CA.
    J Clin Invest; 1988 Sep; 82(3):782-8. PubMed ID: 3417871
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  • 15. Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes.
    Coates PM, Hale DE, Stanley CA, Corkey BE, Cortner JA.
    Pediatr Res; 1985 Jul; 19(7):671-6. PubMed ID: 4022673
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  • 16. A novel disease with deficiency of mitochondrial very-long-chain acyl-CoA dehydrogenase.
    Aoyama T, Uchida Y, Kelley RI, Marble M, Hofman K, Tonsgard JH, Rhead WJ, Hashimoto T.
    Biochem Biophys Res Commun; 1993 Mar 31; 191(3):1369-72. PubMed ID: 8466512
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  • 18. Neonatal screening for very long-chain acyl-coA dehydrogenase deficiency: enzymatic and molecular evaluation of neonates with elevated C14:1-carnitine levels.
    Liebig M, Schymik I, Mueller M, Wendel U, Mayatepek E, Ruiter J, Strauss AW, Wanders RJ, Spiekerkoetter U.
    Pediatrics; 2006 Sep 31; 118(3):1065-9. PubMed ID: 16950999
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