Clinical practice guideline for renal hypouricemia (1st edition)-Reference-Cited by-同舟云学术

Clinical practice guideline for renal hypouricemia (1st edition)

Published:2019-02-19 Issue:2 Volume:32 Page:83-87
ISSN:1749-0774
Container-title:Human Cell
language:en
Short-container-title:Human Cell

Author:

Nakayama Akiyoshi,Matsuo Hirotaka,Ohtahara Akira,Ogino Kazuhide,Hakoda Masayuki,Hamada Toshihiro,Hosoyamada Makoto,Yamaguchi Satoshi,Hisatome Ichiro,Ichida Kimiyoshi,Shinomiya Nariyoshi

Funder

Ministry of Health, Labour and Welfare

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Cell Biology

Link

http://link.springer.com/article/10.1007/s13577-019-00239-3/fulltext.html

Reference15 articles.

1. Akaoka I, Nishizawa T, Yano E, Takeuchi A, Nishida Y. Familial hypouricaemia due to renal tubular defect of urate transport. Ann Clin Res. 1975;7(5):318–24.

2. Wakasugi M, Kazama JJ, Narita I, Konta T, Fujimoto S, Iseki K, et al. Association between hypouricemia and reduced kidney function: a cross-sectional population-based study in Japan. Am J Nephrol. 2015;41(2):138–46. https://doi.org/10.1159/000381106 .

3. Matsuo H, Chiba T, Nagamori S, Nakayama A, Domoto H, Phetdee K, et al. Mutations in glucose transporter 9 gene SLC2A9 cause renal hypouricemia. Am J Hum Genet. 2008;83(6):744–51. https://doi.org/10.1016/j.ajhg.2008.11.001 .

4. Suzuki T, Kidoguchi K, Hayashi A. Genetic heterogeneity of familial hypouricemia due to isolated renal tubular defect. Jinrui Idengaku Zasshi. 1981;26(3):243–8. https://doi.org/10.1007/BF01896136 .

5. Stiburkova B, Gabrikova D, Cepek P, Simek P, Kristian P, Cordoba-Lanus E, et al. Prevalence of URAT1 allelic variants in the Roma population. Nucleosides Nucleotides Nucleic Acids. 2016;35(10–12):529–35. https://doi.org/10.1080/15257770.2016.1168839 .

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