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Journal Abstract Search

168 related items for PubMed ID: 6790859

  • 1.
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  • 2. [Hyperammonemias of childhood. I. Enzymopathies of the urea cycle].
    Kopieczna-Grzebieniak E, Toborek M, Tarnawski R, Jakubowska D.
    Pediatr Pol; 1987 Oct; 62(10):727-32. PubMed ID: 3328149
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  • 3. The ornithine-urea cycle: biosynthesis and regulation of carbamyl phosphate synthetase I and ornithine transcarbamylase.
    Cohen PP.
    Curr Top Cell Regul; 1981 Oct; 18():1-19. PubMed ID: 7023854
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  • 8. [Hereditary hyperammonemia due to qualitative abnormality of hepatic and intestinal ornithine carbamoyl-transferase].
    Cathelineau L, Navarro J, Aymard P, Baudon JJ, Mondet Y, Polonovski C, Laplane R.
    Arch Fr Pediatr; 1972 Oct; 29(7):713-36. PubMed ID: 4644461
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  • 10. Partial ornithine transcarbamylase deficiency in females: diagnosis by an immunohistochemical method.
    Hayasaka K, Metoki K, Ishiguro S, Kato S, Chiba T, Hirooka M, Kikuchi M, Kurobane I, Narisawa K, Tada K.
    Eur J Pediatr; 1987 Jul; 146(4):370-2. PubMed ID: 3308467
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  • 11. [Prenatal diagnosis of carbamyl phosphate synthetase deficiency by fetal liver biopsy].
    Murotsuki J, Uehara S, Okamura K, Yajima A, Kikuchi M, Oura T, Miyabayashi S.
    Nihon Sanka Fujinka Gakkai Zasshi; 1991 Dec; 43(12):1613-6. PubMed ID: 1744457
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  • 13. 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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  • 14. [Hyperammonemia].
    Arashima S.
    Nihon Rinsho; 1978 May 15; Suppl():1352-3. PubMed ID: 691351
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  • 15. Enzymatic analysis of citrullinemia (12 cases) in Japan.
    Saheki T, Ueda A, Hosoya M, Sase M, Nakano K, Katsunuma T.
    Adv Exp Med Biol; 1982 May 15; 153():63-76. PubMed ID: 7164923
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  • 18. Synthesis, intracellular transport, and processing of the precursors for mitochondrial ornithine transcarbamylase and carbamoyl-phosphate synthetase I in isolated hepatocytes.
    Mori M, Morita T, Ikeda F, Amaya Y, Tatibana M, Cohen PP.
    Proc Natl Acad Sci U S A; 1981 Oct 15; 78(10):6056-60. PubMed ID: 6947214
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  • 19. [Molecular genetics of urea cycle diseases].
    Ohtake A, Mori M.
    Seikagaku; 1990 Sep 15; 62(9):1170-7. PubMed ID: 2258657
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  • 20. Prospective treatment of urea cycle disorders.
    Maestri NE, Hauser ER, Bartholomew D, Brusilow SW.
    J Pediatr; 1991 Dec 15; 119(6):923-8. PubMed ID: 1720458
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