275 related articles for article (PubMed ID: 5801674)
1. The conversion of 4-hydroxypyrazolo[3,4-d]pyrimidine (allopurinol) into 4,6-dihroxypyrazolo[3,4-d]pyrimidine (Oxipurinol) in vivo in the absence of xanthine-oxen oxidoreductase.
Chalmers RA; Parker R; Simmonds HA; Snedden W; Watts RW
Biochem J; 1969 May; 112(4):527-32. PubMed ID: 5801674
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Liquid chromatography with multichannel ultraviolet detection used for studying disorders of purine metabolism.
Kojima T; Nishina T; Kitamura M; Kamatani N; Nishioka K
Clin Chem; 1987 Nov; 33(11):2052-6. PubMed ID: 3677379
[TBL] [Abstract][Full Text] [Related]
4. Biochemical studies on the purine metabolism of four cases with hereditary xanthinuria.
Kojima T; Nishina T; Kitamura M; Hosoya T; Nishioka K
Clin Chim Acta; 1984 Feb; 137(2):189-98. PubMed ID: 6423323
[TBL] [Abstract][Full Text] [Related]
5. Variations in allopurinol metabolism by xanthinuric subjects.
Simmonds HA; Levin B; Cameron JS
Clin Sci Mol Med; 1974 Aug; 47(2):173-8. PubMed ID: 4416848
[No Abstract] [Full Text] [Related]
6. [Studies on purine-pyrimidine metabolism (1)--Quantitation of purine-pyrimidine metabolites and allopurinol-oxipurinol in biological fluids].
Hiroshige K; Kunifuji Y; Takasugi M; Kuroiwa A
J UOEH; 1992 Sep; 14(3):211-8. PubMed ID: 1410939
[TBL] [Abstract][Full Text] [Related]
7. Allopurinol metabolism in a patient with xanthine oxidase deficiency.
Yamanaka H; Nishioka K; Suzuki T; Kohno K
Ann Rheum Dis; 1983 Dec; 42(6):684-6. PubMed ID: 6689118
[TBL] [Abstract][Full Text] [Related]
8. [The total absence of xanthine oxidase activity. Apropos 2 cases of the nonfamilial incidence of xanthinuria].
Sastre Pascual JF; Roca Villanueva B; Arenas Jiménez MD; Mengual Alarte MJ; Zamora Navarro S; Boronat Botella M; Arenas Adarve M
An Med Interna; 1991 Apr; 8(4):181-4. PubMed ID: 1912172
[TBL] [Abstract][Full Text] [Related]
9. [The influence of allopurinol on purine- and pyrimidinesynthesis (author's transl)].
Gröbner W; Zöllner N
Klin Wochenschr; 1978 Mar; 53(16):255-60. PubMed ID: 682520
[TBL] [Abstract][Full Text] [Related]
10. Two siblings with classical xanthinuria type 1: significance of allopurinol loading test.
Ichida K; Yoshida M; Sakuma R; Hosoya T
Intern Med; 1998 Jan; 37(1):77-82. PubMed ID: 9510406
[TBL] [Abstract][Full Text] [Related]
11. Metabolism of pyrazinamide and allopurinol in hereditary xanthine oxidase deficiency.
Yamamoto T; Higashino K; Kono N; Kawachi M; Nanahoshi M; Takahashi S; Suda M; Hada T
Clin Chim Acta; 1989 Feb; 180(2):169-75. PubMed ID: 2731378
[TBL] [Abstract][Full Text] [Related]
12. Urinary excretion of 6 hydroxylated metabolite and oxypurines in a xanthinuric man given allopurinol or thiopurinol.
Auscher C; Pasquier C; Mercier N; Delbarre F
Adv Exp Med Biol; 1974; 41():663-7. PubMed ID: 4832593
[No Abstract] [Full Text] [Related]
13. Excretion of hypoxanthine and xanthine in a genetic disease of purine metabolism.
Sweetman L; Nyhan WL
Nature; 1967 Aug; 215(5103):859-60. PubMed ID: 6049739
[No Abstract] [Full Text] [Related]
14. The quantitative determination of hypoxanthine and xanthine ("oxypurines") in skeletal muscle from two patients with congenital xanthine oxidase deficiency (xanthinuria).
Parker R; Snedden W; Watts RW
Biochem J; 1970 Jan; 116(2):317-8. PubMed ID: 5414104
[No Abstract] [Full Text] [Related]
15. Decreased xanthine oxidase activities and increased urinary oxypurines in heterozygotes for hereditary xanthinuria.
Kawachi M; Kono N; Mineo I; Yamada Y; Tarui S
Clin Chim Acta; 1990 Apr; 188(2):137-46. PubMed ID: 2379312
[TBL] [Abstract][Full Text] [Related]
16. [Hereditary xanthinuria. A clinical case report].
Pessano B; Davì S; La Brocca A; Leone L
Minerva Med; 1989 May; 80(5):507-9. PubMed ID: 2747979
[TBL] [Abstract][Full Text] [Related]
17. Hereditary xanthinuria. Evidence for enhanced hypoxanthine salvage.
Mateos FA; Puig JG; Jiménez ML; Fox IH
J Clin Invest; 1987 Mar; 79(3):847-52. PubMed ID: 3818951
[TBL] [Abstract][Full Text] [Related]
18. Xanthine oxidase deficiency: studies of a previously unreported case.
Holmes EW; Mason DH; Goldstein LI; Blount RE; Kelley WN
Clin Chem; 1974 Aug; 20(8):1076-9. PubMed ID: 4369449
[No Abstract] [Full Text] [Related]
19. Hereditary xanthinuria is not so rare disorder of purine metabolism.
Sebesta I; Stiburkova B; Krijt J
Nucleosides Nucleotides Nucleic Acids; 2018; 37(6):324-328. PubMed ID: 29723117
[TBL] [Abstract][Full Text] [Related]
20. Effects of allopurinol and oxipurinol on purine synthesis in cultured human cells.
Kelley WN; Wyngaarden JB
J Clin Invest; 1970 Mar; 49(3):602-9. PubMed ID: 5415686
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
