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Journal Abstract Search

215 related items for PubMed ID: 6763345

  • 21. Hyperammonemia.
    Batshaw ML.
    Curr Probl Pediatr; 1984 Nov; 14(11):1-69. PubMed ID: 6510017
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  • 23. Hereditary urea cycle diseases in Finland.
    Keskinen P, Siitonen A, Salo M.
    Acta Paediatr; 2008 Oct; 97(10):1412-9. PubMed ID: 18616627
    [Abstract] [Full Text] [Related]

  • 24. Prospective treatment of urea cycle disorders.
    Maestri NE, Hauser ER, Bartholomew D, Brusilow SW.
    J Pediatr; 1991 Dec; 119(6):923-8. PubMed ID: 1720458
    [Abstract] [Full Text] [Related]

  • 25. Hereditary disorders of the urea cycle in man: biochemical and molecular approaches.
    Saheki T, Kobayashi K, Inoue I.
    Rev Physiol Biochem Pharmacol; 1987 Dec; 108():21-68. PubMed ID: 3306877
    [No Abstract] [Full Text] [Related]

  • 26. Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis.
    Brusilow SW, Danney M, Waber LJ, Batshaw M, Burton B, Levitsky L, Roth K, McKeethren C, Ward J.
    N Engl J Med; 1984 Jun 21; 310(25):1630-4. PubMed ID: 6427608
    [Abstract] [Full Text] [Related]

  • 27. Histopathological findings in livers of patients with urea cycle disorders.
    Yaplito-Lee J, Chow CW, Boneh A.
    Mol Genet Metab; 2013 Mar 21; 108(3):161-5. PubMed ID: 23403242
    [Abstract] [Full Text] [Related]

  • 28. Detection of urea cycle enzymopathies in childhood.
    Trauner DA, Self TW.
    Arch Neurol; 1984 Jul 21; 41(7):758-60. PubMed ID: 6743067
    [Abstract] [Full Text] [Related]

  • 29. Contrasting features of urea cycle disorders in human patients and knockout mouse models.
    Deignan JL, Cederbaum SD, Grody WW.
    Mol Genet Metab; 2008 Jan 21; 93(1):7-14. PubMed ID: 17933574
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  • 31. Urea cycle disorders: clinical presentation outside the newborn period.
    Smith W, Kishnani PS, Lee B, Singh RH, Rhead WJ, Sniderman King L, Smith M, Summar M.
    Crit Care Clin; 2005 Oct 21; 21(4 Suppl):S9-17. PubMed ID: 16227115
    [Abstract] [Full Text] [Related]

  • 32. Definitive cure of hyperammonemia by liver transplantation in urea cycle defects: report of three cases.
    Jan D, Poggi F, Jouvet P, Rabier D, Laurent J, Beringer A, Hubert P, Saudubray JM, Revillon Y.
    Transplant Proc; 1994 Feb 21; 26(1):188. PubMed ID: 8108934
    [No Abstract] [Full Text] [Related]

  • 33.
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  • 34. Transient hyperammonemias in infants with and without organic acidemia.
    Nyhan WL, Rubio V, Jordá A, Grisolia S, Gutierez F, Canosa C.
    Adv Exp Med Biol; 1982 Feb 21; 153():331-8. PubMed ID: 7164908
    [No Abstract] [Full Text] [Related]

  • 35. Inborn defects of the mitochondrial portion of the urea cycle.
    Colombo JP, Bachmann C, Schrämmli A.
    Ann N Y Acad Sci; 1986 Feb 21; 488():109-17. PubMed ID: 3555250
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  • 40. Diagnosis of urea cycle disorders.
    Palmer T, Oberholzer VG.
    Ann Clin Biochem; 1977 May 21; 14(3):136-8. PubMed ID: 17345
    [No Abstract] [Full Text] [Related]

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