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.
22. An immunoreactive xanthine oxidase protein-possessing xanthinuria and her family. Yamamoto T; Moriwaki Y; Suda M; Takahashi S; Hada T; Nanahoshi M; Agbedana EO; Higashino K Clin Chim Acta; 1992 Jun; 208(1-2):93-8. PubMed ID: 1638758 [TBL] [Abstract][Full Text] [Related]
23. [Some peculiarities of a family with xanthinuria]. Temperville B; Cavelier B; Godin M Nouv Presse Med; 1979 Mar; 8(13):1096-7. PubMed ID: 461140 [No Abstract] [Full Text] [Related]
24. Study of urinary pyrazinamide metabolites and their action on the renal excretion of xanthine and hypoxanthine in a xanthinuric patient. Auscher C; Pasquier C; Pehuet P; Delbarre F Biomedicine; 1978 May; 28(2):129-33. PubMed ID: 667278 [TBL] [Abstract][Full Text] [Related]
26. Pregnancy in and incidence of xanthine oxidase deficiency. Harkness RA; McCreanor GM; Simpson D; MacFadyen IR J Inherit Metab Dis; 1986; 9(4):407-8. PubMed ID: 3104682 [No Abstract] [Full Text] [Related]
27. Clinicobiochemical analysis of four cases of xanthine oxidase deficiency. Nishioka K; Yamanaka H; Nishina T; Hosoya T; Mikanagi K Adv Exp Med Biol; 1984; 165 Pt A():73-6. PubMed ID: 6547018 [No Abstract] [Full Text] [Related]
28. Demonstration of a combined deficiency of xanthine oxidase and aldehyde oxidase in xanthinuric patients not forming oxipurinol. Reiter S; Simmonds HA; Zöllner N; Braun SL; Knedel M Clin Chim Acta; 1990 Mar; 187(3):221-34. PubMed ID: 2323062 [TBL] [Abstract][Full Text] [Related]
29. Hereditary xanthinuria with severe urolithiasis occurring in infancy as renal tubular acidosis and hypercalciuria. Fildes RD J Pediatr; 1989 Aug; 115(2):277-80. PubMed ID: 2754557 [No Abstract] [Full Text] [Related]
30. Hypouricemia and malignant neoplasms. A new case of xanthinuria. Mitnick PD; Beck LH Arch Intern Med; 1979 Oct; 139(10):1186-7. PubMed ID: 485757 [TBL] [Abstract][Full Text] [Related]
31. Some genetical aspects of hyperuricaemia and xanthinuria. Tobias PV S Afr Med J; 1972 Apr; 46(18):552-4. PubMed ID: 5034963 [No Abstract] [Full Text] [Related]
32. The effect of allopurinol on oxypurine excretion in xanthinuria. Salti IS; Kattuah N; Alam S; Wehby V; Frayha R J Rheumatol; 1976 Jun; 3(2):201-4. PubMed ID: 950637 [TBL] [Abstract][Full Text] [Related]
33. [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]
34. [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]
35. Ureteral xanthine calculus and aberrant umbilical artery causing ureteral obstruction. Frankenschmidt A; Pohl M; Zimmerhackl LB; Sommerkamp H Urol Int; 1997; 58(3):189-91. PubMed ID: 9188142 [TBL] [Abstract][Full Text] [Related]
36. [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]
37. [A new method for the determination of xanthine oxidase activity by high-performance liquid chromatography with electrochemical detection]. Kojima T; Nishina T; Yamanaka H Rinsho Byori; 1992 Oct; 40(10):1096-100. PubMed ID: 1307615 [TBL] [Abstract][Full Text] [Related]
38. A xanthinuric family--the proposita having immunologically reactive xanthine oxidase but no xanthine oxidase activity. Yamamoto T; Moriwaki Y; Takahashi S; Hada T; Suda M; Imanishi H; Agbedana OE; Nanahoshi M; Higashino K Adv Exp Med Biol; 1991; 309A():369-72. PubMed ID: 1789246 [TBL] [Abstract][Full Text] [Related]
39. [Xanthinuria type I as the cause of nephrolithiasis in 17-years old girl]. Borucka B; Runowski D; Safranow K; Olszewska M; Jakubowska K; Chlubek D Pol Merkur Lekarski; 2010 Aug; 29(170):111-4. PubMed ID: 20842824 [TBL] [Abstract][Full Text] [Related]
40. Hereditary xanthinuria: report on three patients and short review of the literature. Frayha RA; Salti IS; Arnaout A; Khatchadurian A; Uthman SM Nephron; 1977; 19(6):328-32. PubMed ID: 927625 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]