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.
165 related articles for article (PubMed ID: 5416258)
21. Renal handling of hypoxanthine and xanthine in normal subjects and in cases of idiopathic renal hypouricemia. Kaneko K; Fujimori S; Kanbayashi T; Akaoka I Adv Exp Med Biol; 1989; 253A():309-15. PubMed ID: 2624208 [No Abstract] [Full Text] [Related]
24. Hyperuricosuria and central nervous system dysfunction. Berman PH; Balis ME; Krakoff IH; Dancis J Trans Am Neurol Assoc; 1967; 92():138-42. PubMed ID: 5634009 [No Abstract] [Full Text] [Related]
25. Treatment of gout and hyperuricaemia by benzbromarone, ethyl 2 (dibromo-3,5 hydroxy-4 benzoyl)-3 benzofuran. de Gery A; Auscher C; Saporta L; Delbarre F Adv Exp Med Biol; 1974; 41():683-9. PubMed ID: 4598966 [No Abstract] [Full Text] [Related]
26. 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]
27. Renal excretion of hypoxanthine and xanthine in primary gout. Puig JG; Mateos FA; Jiménez ML; Ramos TH Am J Med; 1988 Oct; 85(4):533-7. PubMed ID: 3177401 [TBL] [Abstract][Full Text] [Related]
28. [Three cases of hereditary xanthinuria: review of the literature (author's transl)]. Temperville B; Godin M; Dubois D; Fillastre JP Sem Hop; 1979 Dec 8-15; 55(41-42):1899-902. PubMed ID: 231309 [TBL] [Abstract][Full Text] [Related]
29. 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 [TBL] [Abstract][Full Text] [Related]
30. [A further case of familial xanthinuria]. Castro-Mendoza HJ; Cifuentes Delatte L; Rapado Errazti A Rev Clin Esp; 1972 Feb; 124(4):341-52. PubMed ID: 5022297 [No Abstract] [Full Text] [Related]
31. [A family of hereditary xanthinuria: two siblings with peptic ulcer and hypouricemia due to xanthine oxidase deficiency, and a heterozygote (father) with gout]. Kawachi M; Kono N; Mineo I; Hara N; Yamada Y; Kiyokawa H; Himeno S; Tarui S; Miyazaki T Nihon Naika Gakkai Zasshi; 1988 Jan; 77(1):47-52. PubMed ID: 3373096 [No Abstract] [Full Text] [Related]
32. [Routine urinary oxypurine assays for the detection of xanthine-oxidase deficiency (author's transl)]. Brault D; Etienne J; Ragot J; Yonger P; Laruelle P Nouv Presse Med; 1982 Mar; 11(14):1059-61. PubMed ID: 7079120 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. [Treatment of gouty purine metabolism disorder with mercapto-pyrazolo-pyrimidine (thiopurinol)]. Delbarre F; Auscher C; de Gery A; Brouilhet H; Olivier JL Presse Med (1893); 1968 Dec; 76(49):2329. PubMed ID: 5737251 [No Abstract] [Full Text] [Related]
36. Hypoxanthine-guanine phosphoribosyltransferase deficiency in gout. Kelley WN; Greene ML; Rosenbloom FM; Henderson JF; Seegmiller JE Ann Intern Med; 1969 Jan; 70(1):155-206. PubMed ID: 4884382 [No Abstract] [Full Text] [Related]
37. 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]