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Journal Abstract Search

315 related items for PubMed ID: 8583741

  • 21. Ornithine transcarbamylase deficiency in the newborn infant.
    Kang ES, Snodgrass PJ, Gerald PS.
    J Pediatr; 1973 Apr; 82(4):642-9. PubMed ID: 4698340
    [No Abstract] [Full Text] [Related]

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  • 24. Inborn errors of urea synthesis.
    Batshaw ML.
    Ann Neurol; 1994 Feb; 35(2):133-41. PubMed ID: 7906500
    [Abstract] [Full Text] [Related]

  • 25. Ornithine transcarbamylase deficiency: a case report.
    Martland T, Mbamali AC, Rittey C, Tanner S, Bonham JR, Griffiths PD.
    Neuropediatrics; 1998 Dec; 29(6):331-2. PubMed ID: 10029357
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  • 27. Double deficiencies of urea cycle enzymes in human liver.
    Raijman L.
    Biochem Med; 1979 Apr; 21(2):226-33. PubMed ID: 465019
    [No Abstract] [Full Text] [Related]

  • 28. Diagnosis of urea cycle disorders.
    Palmer T, Oberholzer VG.
    Ann Clin Biochem; 1977 May; 14(3):136-8. PubMed ID: 17345
    [No Abstract] [Full Text] [Related]

  • 29. [Hereditary enzyme defects of the urea cycle].
    Colombo JP.
    Ergeb Inn Med Kinderheilkd; 1971 May; 31():97-130. PubMed ID: 4933544
    [No Abstract] [Full Text] [Related]

  • 30. [Inborn metabolic errors of urea cycle synthesis. Present possibilities of treatment].
    Sarnavka V, Gjurić G, Milicić D, Granić P, Mardesić D.
    Lijec Vjesn; 1990 May; 112(11-12):397-403. PubMed ID: 2097476
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  • 31. [Metabolic inborn error with acute debut in newborns].
    Reigstad H.
    Tidsskr Nor Laegeforen; 2008 Jun 26; 128(13):1537. PubMed ID: 18604904
    [No Abstract] [Full Text] [Related]

  • 32. Hyperammonemia due to a mutant enzyme of ornithine transcarbamylase.
    Matsuda I, Arashima S, Nambu H, Takekoshi Y, Anakura M.
    Pediatrics; 1971 Oct 26; 48(4):595-600. PubMed ID: 5114747
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  • 34. [Neonatal hyperammonemia].
    Jaeken J, Devlieger H, Evens M, Casaer P, Eggermont E.
    Tijdschr Kindergeneeskd; 1983 Jun 26; 51(3):101-4. PubMed ID: 6636106
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  • 37. Lethal neonatal deficiency of carbamyl phosphate synthetase.
    Gelehrter TD, Snodgrass PJ.
    N Engl J Med; 1974 Feb 21; 290(8):430-3. PubMed ID: 4811018
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  • 39. 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
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  • 40. The sparse fur mouse: an animal model for a human inborn error of metabolism of the urea cycle.
    Spector EB, Mazzocchi RA.
    Prog Clin Biol Res; 1983 Feb 21; 127():85-96. PubMed ID: 6889405
    [No Abstract] [Full Text] [Related]

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