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3. Lesch-Nyhan syndrome. Arima M; Aoki N; Ono K Paediatr Univ Tokyo; 1970 Dec; 18():25-31. PubMed ID: 5514644 [No Abstract] [Full Text] [Related]
4. [Lesh-Nyhan syndrome. A congenital defect of purine metabolism with the clinical symptoms of gout and central nervous disorders]. Kaiser W; Zöllner N Dtsch Med Wochenschr; 1970 May; 95(19):1077-80. PubMed ID: 5424954 [No Abstract] [Full Text] [Related]
7. Studies on the adenine phosphoribosyltransferase enzyme in human fibroblasts lacking hypoxanthine-guanine phosphoribosyltransferase. Kelley WN J Lab Clin Med; 1971 Jan; 77(1):33-8. PubMed ID: 4250494 [No Abstract] [Full Text] [Related]
8. Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase: intermediate enzyme deficiency in heterozygote red cells. Emmerson BT; Wallace DC; Thompson CJ Ann Intern Med; 1972 Feb; 76(2):285-7. PubMed ID: 5009595 [No Abstract] [Full Text] [Related]
9. Seminars on Lesch-Nyhan syndrome. Aspects of purine metabolism. Balis ME Fed Proc; 1968; 27(4):1067-74. PubMed ID: 4968794 [No Abstract] [Full Text] [Related]
10. 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]
11. Hypoxanthine-guanine phosphoribosyltransferase deficiency in the Lesch-Nyhan syndrome and gout. Kelley WN Fed Proc; 1968; 27(4):1047-52. PubMed ID: 5658470 [No Abstract] [Full Text] [Related]
12. Further studies of the enzyme composition of mutant cells in X-linked uric aciduria. Sweetman L; Nyhan WL Arch Intern Med; 1972 Aug; 130(2):214-20. PubMed ID: 5065734 [No Abstract] [Full Text] [Related]
13. [Hyperuricemia and gout in childhood (Lesch-Nyhan syndrome)]. Kölle G Med Klin; 1971 Apr; 66(17):626-30. PubMed ID: 4251840 [No Abstract] [Full Text] [Related]
14. Alterations in the activity of hypoxanthine and adenine phosphoribosyltransferase in patients with hyperuricaemia and gout. Boyle JA; Greene ML; Seegmiller JE Q J Med; 1971 Oct; 40(160):574-5. PubMed ID: 5157418 [No Abstract] [Full Text] [Related]
15. Alteration of purine control mechanisms in patients with the Lesch-Nyhan mutation. Benke PJ Wis Med J; 1971 Jul; 70(7):174-5. PubMed ID: 5560233 [No Abstract] [Full Text] [Related]
16. Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis. Seegmiller JE; Rosenbloom FM; Kelley WN Science; 1967 Mar; 155(3770):1682-4. PubMed ID: 6020292 [TBL] [Abstract][Full Text] [Related]
17. 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 [No Abstract] [Full Text] [Related]
18. [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]
19. 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; 59(3):259-64. PubMed ID: 5444710 [No Abstract] [Full Text] [Related]