155 related articles for article (PubMed ID: 35491177)
1. Xanthinuria Type 1 with a Novel Mutation in Xanthine Dehydrogenase and a Normal Endothelial Function.
Miyazaki S; Hamada T; Sugihara S; Mizuta E; Endo Y; Ohtahara A; Komatsu K; Kuwabara M; Fukuuchi T; Kaneko K; Ichida K; Ogino K; Ninomiya H; Yamamoto K; Nakamura T; Hisatome I
Intern Med; 2022; 61(9):1383-1386. PubMed ID: 35491177
[TBL] [Abstract][Full Text] [Related]
2. Mutational analysis of the xanthine dehydrogenase gene in a Turkish family with autosomal recessive classical xanthinuria.
Gok F; Ichida K; Topaloglu R
Nephrol Dial Transplant; 2003 Nov; 18(11):2278-83. PubMed ID: 14551354
[TBL] [Abstract][Full Text] [Related]
3. A case of xanthinuria type I with a novel mutation in xanthine dehydrogenase.
Iguchi A; Sato T; Yamazaki M; Tasaki K; Suzuki Y; Iino N; Hasegawa H; Ichida K; Narita I
CEN Case Rep; 2016 Nov; 5(2):158-162. PubMed ID: 28508967
[TBL] [Abstract][Full Text] [Related]
4. Identification of a xanthinuria type I case with mutations of xanthine dehydrogenase in an Afghan child.
Nakamura M; Yuichiro Y; Sass JO; Tomohiro M; Schwab KO; Takeshi N; Tatsuo H; Ichida K
Clin Chim Acta; 2012 Dec; 414():158-60. PubMed ID: 22981351
[TBL] [Abstract][Full Text] [Related]
5. [Xanthinuria type 1 in a woman with arthralgias: a combined clinical and molecular genetic investigation].
Därr RW; Lenzner S; Eggermann T; Därr WH
Dtsch Med Wochenschr; 2016 Apr; 141(8):571-4. PubMed ID: 27078247
[TBL] [Abstract][Full Text] [Related]
6. Xanthine dehydrogenase deficiency with novel sequence variations presenting as rheumatoid arthritis in a 78-year-old patient.
Jurecka A; Stiburkova B; Krijt J; Gradowska W; Tylki-Szymanska A
J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S21-4. PubMed ID: 20077140
[TBL] [Abstract][Full Text] [Related]
7. Multi-exon deletion in the XDH gene as a cause of classical xanthinuria.
Eggermann T; Spengler S; Denecke B; Zerres K; Mache CJ
Clin Nephrol; 2013 Jan; 79(1):78-80. PubMed ID: 23249873
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [Type 1 xanthinuria: Report on three cases].
Diss M; Ranchin B; Broly F; Pottier N; Cochat P
Arch Pediatr; 2015 Dec; 22(12):1288-91. PubMed ID: 26521682
[TBL] [Abstract][Full Text] [Related]
10. A case of hereditary xanthinuria type 1 accompanied by bilateral renal calculi.
Fujiwara Y; Kawakami Y; Shinohara Y; Ichida K
Intern Med; 2012; 51(14):1879-84. PubMed ID: 22821105
[TBL] [Abstract][Full Text] [Related]
11. A novel mutation in xanthine dehydrogenase in a case with xanthinuria in Hunan province of China.
Xu T; Xie X; Zhang Z; Zhao N; Deng Y; Li P
Clin Chim Acta; 2020 May; 504():168-171. PubMed ID: 32067994
[TBL] [Abstract][Full Text] [Related]
12. XDH gene mutation is the underlying cause of classical xanthinuria: a second report.
Levartovsky D; Lagziel A; Sperling O; Liberman U; Yaron M; Hosoya T; Ichida K; Peretz H
Kidney Int; 2000 Jun; 57(6):2215-20. PubMed ID: 10844591
[TBL] [Abstract][Full Text] [Related]
13. Using Next-Generation Sequencing to Identify a Mutation in Human MCSU that is Responsible for Type II Xanthinuria.
Zhou Y; Zhang X; Ding R; Li Z; Hong Q; Wang Y; Zheng W; Geng X; Fan M; Cai G; Chen X; Wu D
Cell Physiol Biochem; 2015; 35(6):2412-21. PubMed ID: 25967871
[TBL] [Abstract][Full Text] [Related]
14. Xanthinuria type I with a novel mutation of xanthine dehydrogenase.
Tanaka K; Kanazawa I; Yamasaki H; Hasegawa H; Ichida K; Sugimoto T
Am J Med Sci; 2015 Aug; 350(2):155-6. PubMed ID: 26110747
[No Abstract] [Full Text] [Related]
15. Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans.
Ichida K; Amaya Y; Okamoto K; Nishino T
Int J Mol Sci; 2012 Nov; 13(11):15475-95. PubMed ID: 23203137
[TBL] [Abstract][Full Text] [Related]
16. Xanthinuria type I: a rare cause of urolithiasis.
Arikyants N; Sarkissian A; Hesse A; Eggermann T; Leumann E; Steinmann B
Pediatr Nephrol; 2007 Feb; 22(2):310-4. PubMed ID: 17115198
[TBL] [Abstract][Full Text] [Related]
17. Candidate causative variant for xanthinuria in a Domestic Shorthair cat.
Pritchard E; Samaha G; Mizzi K; Boland L; ; Haase B
Anim Genet; 2023 Aug; 54(4):576-580. PubMed ID: 36970934
[TBL] [Abstract][Full Text] [Related]
18. Thiopurine-induced toxicity is associated with dysfunction variant of the human molybdenum cofactor sulfurase gene (xanthinuria type II).
Stiburkova B; Pavelcova K; Petru L; Krijt J
Toxicol Appl Pharmacol; 2018 Aug; 353():102-108. PubMed ID: 29935280
[TBL] [Abstract][Full Text] [Related]
19. [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]
20. Modern diagnostic approach to hereditary xanthinuria.
Mraz M; Hurba O; Bartl J; Dolezel Z; Marinaki A; Fairbanks L; Stiburkova B
Urolithiasis; 2015 Feb; 43(1):61-7. PubMed ID: 25370766
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]