Increased urinary prostaglandin E2 metabolite: A potential therapeutic target of Gitelman syndrome.

in: PLoS ONE | 2017

von Xiaoyan Peng | Lanping Jiang | Chen Chen | +7

Clinical and Genetic Analysis of Multiple Endocrine Neoplasia Type 1-Related Primary Hyperparathyroidism in Chinese.

in: PLoS ONE | 2016

von Jing Kong | Ou Wang | Min Nie | +7

Novel mutations in FKBP10 and PLOD2 cause rare Bruck syndrome in Chinese patients.

in: PLoS ONE | 2014

von Peiran Zhou | Yi Liu | Fang Lv | +6

Novel HRPT2/CDC73 gene mutations and loss of expression of parafibromin in Chinese patients with clinically sporadic parathyroid carcinomas.

in: PLoS ONE | 2012

von Ou Wang | Chunyan Wang | Min Nie | +7

Novel and recurrent mutations of WISP3 in two Chinese families with progressive pseudorheumatoid dysplasia.

in: PLoS ONE | 2012

von Jing Sun | Weibo Xia | Shuli He | +8

Association of six single nucleotide polymorphisms with gestational diabetes mellitus in a Chinese population.

in: PLoS ONE | 2011

von Ying Wang | Min Nie | Wei Li | +5