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Journal Abstract Search

128 related items for PubMed ID: 4863120

  • 1. [Inborn errors of purine and pyrimidine metabolism].
    Arakawa T, Wada Y.
    Horumon To Rinsho; 1967 Mar; 15(3):245-54. PubMed ID: 4863120
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  • 4. [Treatment of gouty purine metabolism disorder with mercapto-pyrazolo-pyrimidine (thiopurinol)].
    Delbarre F, Auscher C, de Gery A, Brouilhet H, Olivier JL.
    Presse Med (1893); 1968 Dec 14; 76(49):2329. PubMed ID: 5737251
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  • 6. [Attack of gout in a xanthinuric patient].
    Delbarre F, Weissenbach R, Auscher C, de Géry A.
    Nouv Presse Med; 1973 Oct 20; 2(37):2465-6. PubMed ID: 4748648
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  • 8. Pseudouridine metabolism. II. Urinary excretion in gout, psoriasis, leukemia, and heterozygous oroticaciduria.
    WEISSMAN S, EISEN AZ, KARON M.
    J Lab Clin Med; 1962 May 20; 59():852-8. PubMed ID: 14005930
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  • 10. Urinary and cerebrospinal fluid oxypurine levels and allopurinol metabolism in the Lesch-Nyhan syndrome.
    Sweetman L.
    Fed Proc; 1968 May 20; 27(4):1055-9. PubMed ID: 5658472
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  • 14. Hereditary orotic aciduria: long-term therapy with uridine and a trial of uracil.
    Becroft DM, Phillips LI, Simmonds A.
    J Pediatr; 1969 Nov 20; 75(5):885-91. PubMed ID: 5347440
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  • 16. Hereditary orotic aciduria: types I and II.
    Fox RM, Wood MH, Royse-Smith D, O'Sullivan WJ.
    Am J Med; 1973 Dec 20; 55(6):791-8. PubMed ID: 4753642
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  • 17. [Hereditary orotic aciduria].
    Mizuno H, Suchi M, Wada Y.
    Ryoikibetsu Shokogun Shirizu; 1998 Dec 20; (18 Pt 1):484-6. PubMed ID: 9590108
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  • 18. Cellular immune deficiency in two siblings with hereditary orotic aciduria.
    Girot R, Hamet M, Perignon JL, Guesnu M, Fox RM, Cartier P, Durandy A, Griscelli C.
    N Engl J Med; 1983 Mar 24; 308(12):700-4. PubMed ID: 6828110
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  • 19. Hereditary orotic aciduria with normal growth and development.
    Tubergen DG, Krooth RS, Heyn RM.
    Am J Dis Child; 1969 Dec 24; 118(6):864-70. PubMed ID: 5353014
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  • 20. Orotic aciduria, homocystinuria, formiminoglutamic aciduria and megaloblastosis associated with the formiminotransferase/cyclodeaminase deficiency.
    Shin YS, Reiter S, Zelger O, Brünstler I, von Rücker A.
    Adv Exp Med Biol; 1986 Dec 24; 195 Pt A():71-6. PubMed ID: 3728187
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