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Journal Abstract Search

170 related items for PubMed ID: 5009595

  • 21. [Treatment of congenital purine-pyrimidine metabolism anomalies].
    Wada Y.
    Horumon To Rinsho; 1971 Jan; 19(1):16-22. PubMed ID: 4926455
    [No Abstract] [Full Text] [Related]

  • 22. Mechanism of excessive purine biosynthesis in hypoxanthine-guanine phosphoribosyltransferase deficiency.
    Sorensen LB.
    J Clin Invest; 1970 May; 49(5):968-78. PubMed ID: 5441549
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  • 23. Hypoxanthine-guanine phosphoribosyltransferase: characteristics of the mutant enzyme in erythrocytes from patients with the Lesch-Nyhan syndrome.
    Arnold WJ, Meade JC, Kelley WN.
    J Clin Invest; 1972 Jul; 51(7):1805-12. PubMed ID: 4624352
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  • 26. [Lesch-Nyhan syndrome. Heterozygote detection by biochemical selection of the mutant cells and autoradiography].
    Hagemeijer AM, Dodinval P, Andrien JM.
    Humangenetik; 1972 Jul; 15(2):126-35. PubMed ID: 5049065
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  • 31. Determination of urinary purines in hyperuricosuric children by thin-layer chromatography.
    Jones CE, Smith EE, Hicks W, Crowell JW.
    J Lab Clin Med; 1970 Jul; 76(1):163-70. PubMed ID: 5425360
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  • 32. Studies of skin fibroblasts from 10 families with HGPRT deficiency, with reference in X-chromosomal inactivation.
    Migeon BR.
    Am J Hum Genet; 1971 Mar; 23(2):199-210. PubMed ID: 5092480
    [No Abstract] [Full Text] [Related]

  • 33. Rarity of X-linked partial hypoxanthine-guanine phosphoribosyltransferase deficiency in a large gouty population.
    Yü TF, Balis ME, Krenitsky TA, Dancis J, Silvers DN, Elion GB, Gutman AB.
    Ann Intern Med; 1972 Feb; 76(2):255-64. PubMed ID: 5009592
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  • 34. Lesch-Nyhan syndrome: preventive control by prenatal diagnosis.
    Boyle JA, Raivio KO, Astrin KH, Schulman JD, Graf ML, Seegmiller JE, Jacobsen CB.
    Science; 1970 Aug 14; 169(3946):688-9. PubMed ID: 5464303
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  • 35. Disorder of purine metabolism due to partial deficiency of hypoxanthine-guanine phosphoribosyltransferase. A study of a family.
    Kogut MD, Donnell GN, Nyhan WL, Sweetman L.
    Am J Med; 1970 Feb 14; 48(2):148-61. PubMed ID: 5416258
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  • 36. Hyperuricaemia and choreoathetosis in a child without mental retardation or self-mutilation - a new HPRT variant.
    Gottlieb RP, Koppel MM, Nyhan WL, Bakay B, Nissinen E, Borden M, Page T.
    J Inherit Metab Dis; 1982 Feb 14; 5(4):183-6. PubMed ID: 6820438
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  • 38. Gout with purine overproduction due to increased phosphoribosylpyrophosphate synthetase activity.
    Becker MA, Meyer LJ, Seegmiller JE.
    Am J Med; 1973 Aug 14; 55(2):232-42. PubMed ID: 4722859
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  • 40. The influence of adenine on the clinical features and purine metabolism in the Lesch-Nyhan syndrome.
    van der Zee SP, Lommen EJ, Trijbels JM, Schretlen ED.
    Acta Paediatr Scand; 1970 May 14; 59(3):259-64. PubMed ID: 5444710
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