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Journal Abstract Search

168 related items for PubMed ID: 86873

  • 1. Organic acids and Reye's syndrome.
    Applegarth DA, MacLeod PM, Toone JR, Kirby LT, MacLean JR, Mamer OA, Montgomery JA.
    Lancet; 1979 May 26; 1(8126):1147. PubMed ID: 86873
    [No Abstract] [Full Text] [Related]

  • 2. beta-Hydroxy-beta-methyglutaricaciduria presenting as Reye's syndrome.
    Leonard JV, Seakins JW, Griffin NK.
    Lancet; 1979 Mar 24; 1(8117):680. PubMed ID: 85928
    [No Abstract] [Full Text] [Related]

  • 3. Partial carbamyl phosphate synthetase deficiency, simulating Reye's syndrome, in a 9-year-old girl.
    Granot E, Matoth I, Lotan C, Shvil Y, Lijovetzky G, Yatziv S.
    Isr J Med Sci; 1986 Jun 24; 22(6):463-5. PubMed ID: 3759432
    [No Abstract] [Full Text] [Related]

  • 4. [Remarks on a clinical case of partial carbamyl phosphate synthetase deficiency].
    Gomirato G, Giaretto G, Bonomi A, Rossi E, Rovere A, Radeschi G, Crosato M.
    Minerva Pediatr; 1989 Feb 24; 41(2):105-8. PubMed ID: 2739630
    [Abstract] [Full Text] [Related]

  • 5. Recurrent Reye's syndrome without liver lipid deposition.
    Cox KL, Cannon RA.
    Hosp Pract (Hosp Ed); 1981 Feb 24; 16(2):45-51. PubMed ID: 7193176
    [No Abstract] [Full Text] [Related]

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  • 8. [Reye's syndrome].
    Tomaszewski L.
    Pediatr Pol; 1982 Nov 24; 57(11):981-8. PubMed ID: 6763187
    [No Abstract] [Full Text] [Related]

  • 9. Reye's syndrome and aspirin: epidemiological associations and inborn errors of metabolism.
    Lancet; 1987 Aug 22; 2(8556):429-31. PubMed ID: 2887729
    [No Abstract] [Full Text] [Related]

  • 10. Masking by enzyme inhibitor of raised serum glutamate dehydrogenase activity in Reye's syndrome.
    Holt JT, Arvan DA, Mayer TK.
    Lancet; 1983 Jul 02; 2(8340):4-7. PubMed ID: 6134899
    [Abstract] [Full Text] [Related]

  • 11. [Congenital deficiency of ornithine transcarbamylase. Description of 2 clinical cases].
    D'Eufemia P, Corrado G, Sabetta G, Castro M, Martino F, Cantani A, Ruberto U.
    Minerva Pediatr; 1983 Mar 15; 35(5):219-24. PubMed ID: 6343831
    [No Abstract] [Full Text] [Related]

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  • 13. Carbamylphosphate synthetase-I deficiency in a newborn: survival after early diagnosis and therapy.
    Raghavan K, Chabra S, Mondkar J, Aiyar R, Ambani LM, Fernandez A.
    Indian Pediatr; 1991 May 15; 28(5):551-4. PubMed ID: 1752685
    [No Abstract] [Full Text] [Related]

  • 14. Liver ultrastructure in mitochondrial urea cycle enzyme deficiencies and comparison with Reye's syndrome.
    Latham PS, LaBrecque DR, McReynolds JW, Klatskin G.
    Hepatology; 1984 May 15; 4(3):404-7. PubMed ID: 6724509
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  • 16. Postpartum coma and death due to carbamoyl-phosphate synthetase I deficiency.
    Wong LJ, Craigen WJ, O'Brien WE.
    Ann Intern Med; 1994 Feb 01; 120(3):216-7. PubMed ID: 8273985
    [No Abstract] [Full Text] [Related]

  • 17. Use of citrulline as a diagnostic marker in the prospective treatment of urea cycle disorders.
    Batshaw ML, Berry GT.
    J Pediatr; 1991 Jun 01; 118(6):914-7. PubMed ID: 2040929
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