[HTML] from revistanefrologia.comNE Martín… - Nefrología, 2011 - revistanefrologia.com ... From a nephrological point of view, it is worth highlighting the hypouricemia associated with hereditaryxanthinuria (autosomal recessive deficiency of the xanthine oxidase enzyme), as it is a severe hypouricemia of less than 1mg/dl associated with a decreased uric acid ... Related articles - Cached - All 3 versions
[PDF] from biomedcentral.comJ Buitkamp, S Joerdis… - BMC genetics, 2011 - biomedcentral.com ... 3177. 22. Simmonds HA, Reiter S, Nishino T: Hereditaryxanthinuria. In The metabolic and molecular bases of inherited disease. Edited by Scriver C, Beaudet A, Sly W, Valle D. New York: McGraw-Hill; 1995: 1781-1797 23. ... Related articles - All 7 versions
[PDF] from amuj.irA Eidi, M Al-Ebrahim, M Eidi, A Haeri Rohani… - Arak Medical University …, 2011 - amuj.ir Page 1. 69 Arak Medical University Journal (AMUJ) Original Article 2011; 14(54): 69-77 The effect of sodium molybdate on decreasing CCl4-induced tissue injury in rats Eidi A(PhD) 1*, Al-Ebrahim M(MSc) 2, Eidi M(PhD) 3, Haeri Rohani A(PhD) 1, Mortazavi P(PhD)4 ... All 4 versions
E Garattini… - Drug Metabolism Reviews, 2011 - informahealthcare.com ... 2008). Single genetic deficits of AOX1 have never been described in humans or other animals, whereas combined deficiency of human XOR and AOX1 is known as type II xanthinuria (Gok et al., 2003; Zannolli et al., 2003). The ... Cited by 1 - Related articles - All 2 versions
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