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Journal Abstract Search

205 related items for PubMed ID: 8208992

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  • 4. Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake.
    Stanley CA, DeLeeuw S, Coates PM, Vianey-Liaud C, Divry P, Bonnefont JP, Saudubray JM, Haymond M, Trefz FK, Breningstall GN.
    Ann Neurol; 1991 Nov; 30(5):709-16. PubMed ID: 1763895
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  • 5. Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndrome.
    Chapoy PR, Angelini C, Brown WJ, Stiff JE, Shug AL, Cederbaum SD.
    N Engl J Med; 1980 Dec 11; 303(24):1389-94. PubMed ID: 7432384
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  • 6. Reye syndrome: rate of oxidation of fatty acids in leukocytes and serum levels of lipid peroxides.
    Yoshida Y, Singh I, Singh AK, Tecklenberg FW, Brown FR, Darby CP.
    J Exp Pathol; 1989 Dec 11; 4(3):133-9. PubMed ID: 2769452
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  • 7. Inherited disorders of mitochondrial fatty acid oxidation: a new responsibility for the neonatologist.
    Roe CR.
    Semin Neonatol; 2002 Feb 11; 7(1):37-47. PubMed ID: 12069537
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  • 8. Defects in mitochondrial fatty acid oxidation: clinical presentations and their role in sudden infant death.
    Pollitt RJ.
    Padiatr Padol; 1993 Feb 11; 28(1):13-7. PubMed ID: 8446423
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  • 9. [Mitochondrial beta-oxidation defects: overview].
    Yamaguchi S.
    Ryoikibetsu Shokogun Shirizu; 2001 Feb 11; (36):60-4. PubMed ID: 11596451
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  • 10. [Mitochondrial beta-oxidation defects].
    Woldseth B, Rootwelt T.
    Tidsskr Nor Laegeforen; 2006 Mar 09; 126(6):756-9. PubMed ID: 16541168
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  • 11. Implications of impaired ketogenesis in fatty acid oxidation disorders.
    Olpin SE.
    Prostaglandins Leukot Essent Fatty Acids; 2004 Mar 09; 70(3):293-308. PubMed ID: 14769488
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  • 15. Mass spectrometric identification of abnormal aromatic compounds in the urine of a child with Reye's like syndrome.
    Rocchiccioli F, Cartier PH, Bougnères PF.
    Biomed Mass Spectrom; 1984 Mar 09; 11(3):127-31. PubMed ID: 6722284
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  • 16. [Reye's syndrome].
    Berghuis M, van Vught AJ, de Klerk JB, Huber J.
    Tijdschr Kindergeneeskd; 1987 Dec 09; 55(6):216-25. PubMed ID: 3327194
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  • 17. Mitochondrial fatty acid oxidation disorders and cyclic vomiting syndrome.
    Rinaldo P.
    Dig Dis Sci; 1999 Aug 09; 44(8 Suppl):97S-102S. PubMed ID: 10490047
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  • 19. Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.
    Treem WR, Rinaldo P, Hale DE, Stanley CA, Millington DS, Hyams JS, Jackson S, Turnbull DM.
    Hepatology; 1994 Feb 09; 19(2):339-45. PubMed ID: 8294091
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