Author:
Arikyants Nina,Sarkissian Ashot,Hesse Albrecht,Eggermann Thomas,Leumann Ernst,Steinmann Beat
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology and Child Health
Reference17 articles.
1. Raivio KO, Saksela M, Lapatto R (2001) Xanthine oxidoreductase: role in human pathophysiology and in hereditary xanthinuria. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited diseases, 8th edn. McGraw-Hill, New York, pp 2639–2652
2. Watts RWE, Engelman K, Klinenberg JR, Seegmiller JE, Sjoerdsma A (1964) Enzyme defect in a case of xanthinuria. Nature 201:395–396
3. Ichida K, Amaya Y, Kamatani N, Nishino T, Hosoya T, Sakai O (1997) Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria. J Clin Invest 99:2391–2397
4. Bradbury MG, Henderson M, Brocklebank JT, Simmonds HA (1995) Acute renal failure due to xanthine stones. Pediatr Nephrol 9:476–477
5. Frayha RA, Salti IS, Arnaout A, Khatchadurian A, Uthman SM (1977) Hereditary xanthinuria: report on three patients and short review of the literature. Nephron 19:328–332
Cited by
56 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献