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5 in total

Review 1. Pharmacogenetic determinants of mercaptopurine disposition in children with acute lymphoblastic leukemia.

Authors: Tiphaine Adam de Beaumais; Evelyne Jacqz-Aigrain
Journal: Eur J Clin Pharmacol Date: 2012-03-16 Impact factor: 2.953

2. Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria.

Authors: K Ichida; Y Amaya; N Kamatani; T Nishino; T Hosoya; O Sakai
Journal: J Clin Invest Date: 1997-05-15 Impact factor: 14.808

3. Modern diagnostic approach to hereditary xanthinuria.

Authors: Martin Mraz; Olha Hurba; Josef Bartl; Zdenek Dolezel; Anthony Marinaki; Lynette Fairbanks; Blanka Stiburkova
Journal: Urolithiasis Date: 2014-11-06 Impact factor: 3.436

Review 4. Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans.

Authors: Kimiyoshi Ichida; Yoshihiro Amaya; Ken Okamoto; Takeshi Nishino
Journal: Int J Mol Sci Date: 2012-11-21 Impact factor: 5.923

5. Association between xanthine dehydrogenase tag single nucleotide polymorphisms and essential hypertension.

Authors: Baogang Wu; Ying Hao; Jin Shi; Ning Geng; Tiejun Li; Yanli Chen; Zhaoqing Sun; Liqiang Zheng; Hong Li; Naijing Li; Xingang Zhang; Yingxian Sun
Journal: Mol Med Rep Date: 2015-07-29 Impact factor: 2.952

5 in total