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32. Overproduction of uric acid in hypoxanthine-guanine phosphoribosyltransferase deficiency. Contribution by impaired purine salvage. Edwards NL; Recker D; Fox IH J Clin Invest; 1979 May; 63(5):922-30. PubMed ID: 447834 [TBL] [Abstract][Full Text] [Related]
33. Genotypic and phenotypic spectrum in attenuated variants of Lesch-Nyhan disease. Fu R; Chen CJ; Jinnah HA Mol Genet Metab; 2014 Aug; 112(4):280-5. PubMed ID: 24930028 [TBL] [Abstract][Full Text] [Related]
34. [Xanthinuria with xanthine lithiasis in a patient with Lesch-Nyhan syndrome under allopurinol therapy]. Rebentisch G; Stolz S; Muche J Aktuelle Urol; 2004 Jun; 35(3):215-21. PubMed ID: 15258855 [TBL] [Abstract][Full Text] [Related]
35. Asymptomatic hyperuricemia: to treat or not to treat. Dincer HE; Dincer AP; Levinson DJ Cleve Clin J Med; 2002 Aug; 69(8):594, 597, 600-2 passim. PubMed ID: 12184468 [TBL] [Abstract][Full Text] [Related]
36. Plasma and urinary oxypurines in Lesch-Nyhan patient after allopurinol treatment. Roscioni G; Farnetani MA; Pagani R; Pizzichini M; Marinello E; Porcelli B Adv Exp Med Biol; 1994; 370():357-61. PubMed ID: 7660928 [No Abstract] [Full Text] [Related]
37. [Report of a patient with Lesch-Nyhan syndrome caused by total deficiency of HGPRT and with normal activity in female family members]. Ferrández A; Mayayo E; Nyhan WL; Bakay B An Esp Pediatr; 1982 Jul; 17(1):60-4. PubMed ID: 7137725 [TBL] [Abstract][Full Text] [Related]
38. HGPRT structural gene mutation in Lesch-Nyhan-syndrome as indicated by antigenic activity and reversion of the enzyme deficiency. Strauss M; Lübbe L; Geissler E Hum Genet; 1981; 57(2):185-8. PubMed ID: 7228031 [TBL] [Abstract][Full Text] [Related]