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.
129 related articles for article (PubMed ID: 7452437)
1. Two successive pregnancies in a woman with xanthinuria: unexpected increase in serum uric acid levels. Uzan S; Beaufils M; Ragot J; Brault D; Donsimoni R J Perinat Med; 1980; 8(6):284-7. PubMed ID: 7452437 [TBL] [Abstract][Full Text] [Related]
2. Asymptomatic xanthinuria detected as a result of routine analysis of serum for urate. Bennett MJ; Carpenter KH; Hill PG Clin Chem; 1985 Mar; 31(3):492. PubMed ID: 3971577 [No Abstract] [Full Text] [Related]
4. A new case with hereditary xanthinuria: response to exercise. Landaas S; Borch K; Aagaard E Clin Chim Acta; 1989 May; 181(2):119-24. PubMed ID: 2736776 [TBL] [Abstract][Full Text] [Related]
6. [Hypouricemia and xanthinuria. Observation of 3 cases]. Morini PL; Bandinelli R; Curiel P Minerva Med; 1979 Mar; 70(12):873-8. PubMed ID: 431842 [TBL] [Abstract][Full Text] [Related]
7. [Unmeasurable uric acid in blood and urine; xanthine dehydrogenase deficiency (or hereditary xanthinuria)]. Mayaudon H; Bauduceau B; Dupuy O; Ceppa F; Roul G; Burnat P Rev Med Interne; 1999 May; 20(5):445. PubMed ID: 10365419 [No Abstract] [Full Text] [Related]
8. 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]
9. Effect of fructose infusion in hereditary xanthinuria. Mateos FA; Puig JG; Ramos TH; Fox IH Adv Exp Med Biol; 1986; 195 Pt A():115-21. PubMed ID: 3728145 [No Abstract] [Full Text] [Related]
10. [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]
11. [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]
12. 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]
15. 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]
16. Xanthinuria: a new case. Kennedy JH; Semmence AM Clin Chem; 1980 Nov; 26(12):1758-9. PubMed ID: 7428164 [No Abstract] [Full Text] [Related]
17. 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]
18. 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]
19. [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]
20. [A case of Xanthinuria in a patient with marked hypouricemia]. Martella V; Sozzo E; Montagna E; Stefanizzi S; Cito A; Marinello E; Terzuoli L; Micheli V; Napoli M G Ital Nefrol; 2011; 28(6):648-53. PubMed ID: 22167616 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]