These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
4. [Gene therapy for genetic disorders of purine metabolism]. Hidaka Y Nihon Rinsho; 1996 Dec; 54(12):3374-8. PubMed ID: 8976123 [TBL] [Abstract][Full Text] [Related]
5. Gene replacement therapy for inborn errors of purine metabolism. Nelson DL; Chang SM; Henkel-Tigges J; Wager-Smith K; Belmont JW; Caskey CT Cold Spring Harb Symp Quant Biol; 1986; 51 Pt 2():1065-71. PubMed ID: 3555977 [TBL] [Abstract][Full Text] [Related]
6. Genetic defects in human purine and pyrimidine metabolism. Boss GR; Seegmiller JE Annu Rev Genet; 1982; 16():297-328. PubMed ID: 6297375 [No Abstract] [Full Text] [Related]
7. [Hereditary anomalies of purine metabolism. Current biochemical aspects]. Perignon JL; Cartier P Arch Fr Pediatr; 1980 Oct; 37(8):487-90. PubMed ID: 6255885 [No Abstract] [Full Text] [Related]
9. First trimester diagnosis of Lesch-Nyhan syndrome: applications to other disorders of purine metabolism. Stout JT; Jackson LG; Caskey CT Prenat Diagn; 1985; 5(3):183-9. PubMed ID: 3927283 [TBL] [Abstract][Full Text] [Related]
10. Disorders associated with purine and pyrimidine metabolism. Edwards NL; Fox IH Spec Top Endocrinol Metab; 1984; 6():95-140. PubMed ID: 6098039 [TBL] [Abstract][Full Text] [Related]
12. Heberden oration 1979: human aberrations of purine metabolism and their significance for rheumatology. Seegmiller JE Ann Rheum Dis; 1980 Apr; 39(2):103-17. PubMed ID: 6247984 [No Abstract] [Full Text] [Related]
14. EHNA is a poor inhibitor of deoxyadenosine catabolism in cultured human lymphocytes. Goday A; Simmonds HA; Webster DR; Morris GS Rev Esp Fisiol; 1985 Mar; 41(1):49-54. PubMed ID: 3923578 [TBL] [Abstract][Full Text] [Related]
15. Efficacy and safety of allopurinol in patients with the Lesch-Nyhan syndrome and partial hypoxanthine- phosphoribosyltransferase deficiency: a follow-up study of 18 Spanish patients. Torres RJ; Prior C; Puig JG Nucleosides Nucleotides Nucleic Acids; 2006; 25(9-11):1077-82. PubMed ID: 17065067 [TBL] [Abstract][Full Text] [Related]
16. 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 [TBL] [Abstract][Full Text] [Related]
17. Decreased S-adenosylhomocysteine hydrolase in inborn errors of purine metabolism. Kaminska JE; Fox IH J Lab Clin Med; 1980 Jul; 96(1):141-7. PubMed ID: 7391654 [TBL] [Abstract][Full Text] [Related]
18. Purine metabolism in cultured human fibroblasts derived from patients deficient in enzymes of the purine salvage pathway. Thompson LF; Willis RC; Stoop JW; Seegmiller JE Monogr Hum Genet; 1978; 10():100-3. PubMed ID: 102920 [No Abstract] [Full Text] [Related]
19. Purine and pyrimidine metabolism. Ciba Found Symp; 1977; (48):331-55. PubMed ID: 245993 [No Abstract] [Full Text] [Related]
20. Efficacy and safety of allopurinol in patients with hypoxanthine-guanine phosphoribosyltransferase deficiency. Torres RJ; Prior C; Puig JG Metabolism; 2007 Sep; 56(9):1179-86. PubMed ID: 17697859 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]