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.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
145 related items for PubMed ID: 4832599
1. The clinical significance of hypouricemia. Ramsdell CM, Kelley WN. Adv Exp Med Biol; 1974; 41():709-16. PubMed ID: 4832599 [No Abstract] [Full Text] [Related]
3. [Typing of hypouricemia (uric acid clearance)]. Tsutani H, Takagi K. Nihon Rinsho; 2003 Jan 20; 61 Suppl 1():357-60. PubMed ID: 12629746 [No Abstract] [Full Text] [Related]
4. Hypouricemia due to renal uricosuria. A case study. Khachadurian AK, Arslanian MJ. Ann Intern Med; 1973 Apr 20; 78(4):547-50. PubMed ID: 4694039 [No Abstract] [Full Text] [Related]
6. Efficacy and safety of allopurinol in patients with hypoxanthine-guanine phosphoribosyltransferase deficiency. Torres RJ, Prior C, Puig JG. Metabolism; 2007 Sep 20; 56(9):1179-86. PubMed ID: 17697859 [Abstract] [Full Text] [Related]
7. The pig as an animal model for purine metabolic studies. Cameron JS, Simmonds HA, Hatfield PJ, Jones AS, Cadenhead A. Adv Exp Med Biol; 1974 Sep 20; 41():691-2. PubMed ID: 4832596 [No Abstract] [Full Text] [Related]
8. Xanthine oxidase deficiency: studies of a previously unreported case. Holmes EW, Mason DH, Goldstein LI, Blount RE, Kelley WN. Clin Chem; 1974 Aug 20; 20(8):1076-9. PubMed ID: 4369449 [No Abstract] [Full Text] [Related]
9. Allopurinol, purines, and pyrimidines. Lancet; 1971 Jan 09; 1(7689):73. PubMed ID: 4099227 [No Abstract] [Full Text] [Related]
10. Hereditary xanthinuria is not so rare disorder of purine metabolism. Sebesta I, Stiburkova B, Krijt J. Nucleosides Nucleotides Nucleic Acids; 2018 Jan 09; 37(6):324-328. PubMed ID: 29723117 [Abstract] [Full Text] [Related]
11. 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 30; 188(2):137-46. PubMed ID: 2379312 [Abstract] [Full Text] [Related]
12. Suppression of uric acid secretion in a patient with renal hypouricemia. Simkin PA, Skeith MD, Healey LA. Adv Exp Med Biol; 1974 Apr 30; 41():723-8. PubMed ID: 4832601 [No Abstract] [Full Text] [Related]
13. The physiologic approach to hyperuricemia. Rastegar A, Thier SO. N Engl J Med; 1972 Mar 02; 286(9):470-6. PubMed ID: 4550616 [No Abstract] [Full Text] [Related]
14. [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 14; 76(49):2329. PubMed ID: 5737251 [No Abstract] [Full Text] [Related]
15. 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 Dec 14; 253A():309-15. PubMed ID: 2624208 [No Abstract] [Full Text] [Related]
16. The influence of allopurinol on renal deterioration in familial nepropathy associated with hyperuricemia (FNAH). The Spanish Group for the Study of FNAH. Miranda ME. Adv Exp Med Biol; 1994 Dec 14; 370():61-4. PubMed ID: 7660979 [No Abstract] [Full Text] [Related]
17. [Hypouricemia--definition and classification]. Fujimori S. Nihon Rinsho; 2003 Jan 14; 61 Suppl 1():353-6. PubMed ID: 12629745 [No Abstract] [Full Text] [Related]
18. Variations in allopurinol metabolism by xanthinuric subjects. Simmonds HA, Levin B, Cameron JS. Clin Sci Mol Med; 1974 Aug 14; 47(2):173-8. PubMed ID: 4416848 [No Abstract] [Full Text] [Related]
19. Two siblings with classical xanthinuria type 1: significance of allopurinol loading test. Ichida K, Yoshida M, Sakuma R, Hosoya T. Intern Med; 1998 Jan 14; 37(1):77-82. PubMed ID: 9510406 [Abstract] [Full Text] [Related]
20. Some genetical aspects of hyperuricaemia and xanthinuria. Tobias PV. S Afr Med J; 1972 Apr 29; 46(18):552-4. PubMed ID: 5034963 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]