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Journal Abstract Search

209 related items for PubMed ID: 3315071

  • 1. Inborn errors of the urea cycle.
    Walter JH, Leonard JV.
    Br J Hosp Med; 1987 Sep; 38(3):176-83. PubMed ID: 3315071
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  • 6. New approaches to the diagnosis and treatment of inborn errors or urea synthesis.
    Batshaw ML, Thomas GH, Brusilow SW.
    Pediatrics; 1981 Aug; 68(2):290-7. PubMed ID: 7267240
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  • 7. Inborn errors of organic acid metabolism.
    Green A.
    Br J Hosp Med; 1989 May; 41(5):426-30, 432, 434. PubMed ID: 2663104
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  • 10. Inborn errors of urea synthesis.
    Batshaw ML.
    Ann Neurol; 1994 Feb; 35(2):133-41. PubMed ID: 7906500
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  • 13. [Diagnosis and acute treatment of inborn metabolic diseases in infants].
    Lund AM, Christensen E, Skovby F.
    Ugeskr Laeger; 2002 Nov 25; 164(48):5613-9. PubMed ID: 12523004
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  • 14. [Inherited hyperammonemia].
    Bik-Multanowski M.
    Przegl Lek; 1998 Nov 25; 55(6):337-41. PubMed ID: 9857711
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  • 17. Organic acidemias.
    Mahoney MJ.
    Clin Perinatol; 1976 Mar 25; 3(1):61-78. PubMed ID: 8230
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  • 19. Congenital disorders of the urea cycle and ammonia detoxication.
    Colombo JP.
    Monogr Paediatr; 1971 Mar 25; 1():1-150. PubMed ID: 4946766
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  • 20. Potential for the prenatal diagnosis of hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome.
    Chadefaux B, Bonnefont JP, Rabier D, Shih VE, Saudubray JM, Kamoun P.
    Am J Med Genet; 1989 Feb 25; 32(2):264. PubMed ID: 2929667
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