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Journal Abstract Search

159 related items for PubMed ID: 3339736

  • 1. Hereditary xanthinuria in 2 Pakistani sisters: asymptomatic in one with beta-thalassemia but causing xanthine stone, obstructive uropathy and hypertension in the other.
    Maynard J, Benson P.
    J Urol; 1988 Feb; 139(2):338-9. PubMed ID: 3339736
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  • 5. A new case with hereditary xanthinuria: response to exercise.
    Landaas S, Borch K, Aagaard E.
    Clin Chim Acta; 1989 May 15; 181(2):119-24. PubMed ID: 2736776
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  • 6. Excretion of hypoxanthine and xanthine in a genetic disease of purine metabolism.
    Sweetman L, Nyhan WL.
    Nature; 1967 Aug 19; 215(5103):859-60. PubMed ID: 6049739
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  • 7. Decreased xanthine oxidase activities and increased urinary oxypurines in heterozygotes for hereditary xanthinuria.
    Kawachi M, Kono N, Mineo I, Yamada Y, Tarui S.
    Clin Chim Acta; 1990 Apr 30; 188(2):137-46. PubMed ID: 2379312
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  • 14. Comparison of capillary electrophoretic and liquid chromatographic determination of hypoxanthine and xanthine for the diagnosis of xanthinuria.
    Bory C, Chantin C, Boulieu R.
    J Chromatogr A; 1996 Apr 12; 730(1-2):329-31. PubMed ID: 8680593
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  • 15. Purine excretion during tumor lysis in children with acute lymphocytic leukemia receiving allopurinol: relationship to acute renal failure.
    Andreoli SP, Clark JH, McGuire WA, Bergstein JM.
    J Pediatr; 1986 Aug 12; 109(2):292-8. PubMed ID: 3461147
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  • 16. [Xanthine oxidase deficiency (hereditary xanthinuria), molybdenum cofactor deficiency].
    Sumi S, Wada Y.
    Nihon Rinsho; 1996 Dec 12; 54(12):3333-6. PubMed ID: 8976115
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