Literature DB >> 17445045

Human uric acid transporter 1 gene analysis in familial renal hypo-uricemia associated with exercise-induced acute renal failure.

Yasufumi Ohtsuka1, Masafumi Zaitsu, Kimiyoshi Ichida, Naoko Isomura, Kosuke Tsuji, Tadashi Sato, Yuhei Hamasaki.   

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Year:  2007        PMID： 17445045     DOI： 10.1111/j.1442-200X.2007.02337.x

Source DB:  PubMed          Journal:  Pediatr Int        ISSN： 1328-8067            Impact factor:   1.524


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  3 in total

1.  Renal hypouricemia caused by novel compound heterozygous mutations in the SLC22A12 gene: a case report with literature review.

Authors:  Zhaowei Zhou; Lidan Ma; Juan Zhou; Zhijian Song; Jinmai Zhang; Ke Wang; Boyu Chen; Dun Pan; Zhiqiang Li; Changgui Li; Yongyong Shi
Journal:  BMC Med Genet       Date:  2018-08-10       Impact factor: 2.103

2.  Non-urate transporter 1, non-glucose transporter member 9-related renal hypouricemia and acute renal failure accompanied by hyperbilirubinemia after anaerobic exercise: a case report.

Authors:  Yoshitaka Furuto; Mariko Kawamura; Akio Namikawa; Hiroko Takahashi; Yuko Shibuya; Takayasu Mori; Eisei Sohara
Journal:  BMC Nephrol       Date:  2019-11-26       Impact factor: 2.388

3.  Transplantation of a kidney with a heterozygous mutation in the SLC22A12 (URAT1) gene causing renal hypouricemia: a case report.

Authors:  Kiyokazu Tsuji; Mineaki Kitamura; Kumiko Muta; Yasushi Mochizuki; Takayasu Mori; Eisei Sohara; Shinichi Uchida; Hideki Sakai; Hiroshi Mukae; Tomoya Nishino
Journal:  BMC Nephrol       Date:  2020-07-16       Impact factor: 2.388
  3 in total

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