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Journal Abstract Search

175 related items for PubMed ID: 6724509

  • 1. Liver ultrastructure in mitochondrial urea cycle enzyme deficiencies and comparison with Reye's syndrome.
    Latham PS, LaBrecque DR, McReynolds JW, Klatskin G.
    Hepatology; 1984; 4(3):404-7. PubMed ID: 6724509
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  • 2. Transiently reduced activity of carbamyl phosphate synthetase and ornithine transcarbamylase in liver of children with Reye's syndrome.
    Brown T, Hug G, Lansky L, Bove K, Scheve A, Ryan M, Brown H, Schubert WK, Partin JC, Lloyd-Still J.
    N Engl J Med; 1976 Apr 15; 294(16):861-7. PubMed ID: 175276
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  • 6. Carbamyl phosphate synthetase and ornithine transcarbamylase activities in enzyme-deficient human liver measured by radiochromatography and correlated with outcome.
    Tuchman M, Tsai MY, Holzknecht RA, Brusilow SW.
    Pediatr Res; 1989 Jul 15; 26(1):77-82. PubMed ID: 2771513
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  • 7. Autosomal recessive inheritance of human mitochondrial carbamyl phosphate synthetase deficiency.
    McReynolds JW, Crowley B, Mahoney MJ, Rosenberg LE.
    Am J Hum Genet; 1981 May 15; 33(3):345-53. PubMed ID: 7246541
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  • 8. Editorial: Ammonia disposal in Reye's syndrome.
    Smith AL.
    N Engl J Med; 1976 Apr 15; 294(16):897-8. PubMed ID: 1250317
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  • 10. [Reye's syndrome].
    Tomaszewski L.
    Pediatr Pol; 1982 Nov 15; 57(11):981-8. PubMed ID: 6763187
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  • 12. Ultrastructural abnormalities of liver cells in Reye's syndrome.
    Iancu TC, Mason WH, Neustein HB.
    Hum Pathol; 1977 Jul 15; 8(4):421-31. PubMed ID: 892794
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  • 14. Hyperornithinemia, hyperammonemia, and homocitrullinuria associated with decreased carbamyl phosphate synthetase I activity.
    Gatfield PD, Taller E, Wolfe DM, Haust MD.
    Pediatr Res; 1975 May 15; 9(5):488-97. PubMed ID: 166348
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  • 15. Immunochemical analysis of carbamyl phosphate synthetase I and ornithine transcarbamylase deficient livers: elevated N-acetylglutamate level in a liver lacking carbamyl phosphate synthetase protein.
    Zhang W, Holzknecht RA, Butkowski RJ, Tuchman M.
    Clin Invest Med; 1990 Aug 15; 13(4):183-8. PubMed ID: 2208834
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  • 16. Abnormalities of hepatic mitochondrial urea-cycle enzyme activities and hepatic ultrastructure in acute fatty liver of pregnancy.
    Weber FL, Snodgrass PJ, Powell DE, Rao P, Huffman SL, Brady PG.
    J Lab Clin Med; 1979 Jul 15; 94(1):27-41. PubMed ID: 469376
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  • 18. Pathology of the liver in Reye's syndrome.
    Svoboda DJ, Reddy JK.
    Lab Invest; 1975 May 15; 32(5):571-9. PubMed ID: 1127876
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  • 20. Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.
    Brusilow SW.
    J Clin Invest; 1984 Dec 15; 74(6):2144-8. PubMed ID: 6511918
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