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Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system.
Rao J, Liu X, Mao J, Tang X, Shen Q, Li G, Sun L, Bi Y, Wang X, Qian Y, Wu B, Wang H, Zhou W, Ma D, Zheng B, Shen Y, Chen Z, Luan J, Wang X, Wang M, Dang X, Wang Y, Wu Y, Hou L, Sun S, Li Q, Liu X, Bai H, Yang Y, Shao X, Li Y, Zheng S, Han M, Liu C, Cao G, Zhao L, Qiu S, Dong Y, Zhu Y, Wang F, Zhang D, Li Y, Zhao L, Yang C, Luo X, Chen L, Jiang X, Zhang A, Xu H; for “Internet Plus” Nephrology Alliance of National Center for Children's Care. Rao J, et al. Among authors: zhang a, zhang d. Clin Genet. 2019 Nov;96(5):402-410. doi: 10.1111/cge.13606. Epub 2019 Jul 25. Clin Genet. 2019. PMID: 31328266
Advance of autophagy in chronic kidney diseases.
Deng X, Xie Y, Zhang A. Deng X, et al. Among authors: zhang a. Ren Fail. 2017 Nov;39(1):306-313. doi: 10.1080/0886022X.2016.1274662. Ren Fail. 2017. PMID: 28085532 Free PMC article. Review.
Acute Kidney Injury among Hospitalized Children in China.
Xu X, Nie S, Zhang A, Mao J, Liu HP, Xia H, Xu H, Liu Z, Feng S, Zhou W, Liu X, Yang Y, Tao Y, Feng Y, Chen C, Wang M, Zha Y, Feng JH, Li Q, Ge S, Chen J, He Y, Teng S, Hao C, Liu BC, Tang Y, He W, He P, Hou FF. Xu X, et al. Among authors: zhang a. Clin J Am Soc Nephrol. 2018 Dec 7;13(12):1791-1800. doi: 10.2215/CJN.00800118. Epub 2018 Oct 4. Clin J Am Soc Nephrol. 2018. PMID: 30287424 Free PMC article.
Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease.
Ye Q, Shen Q, Rao J, Zhang A, Zheng B, Liu X, Shen Y, Chen Z, Wu Y, Hou L, Jian S, Wei M, Ma M, Sun S, Li Q, Dang X, Wang Y, Xu H, Mao J; for Chinese Children Genetic Kidney Disease Database (CCGKDD), “Internet Plus” Nephrology Alliance of National Center for Children's Care. Ye Q, et al. Among authors: zhang a. Clin Genet. 2020 Mar;97(3):407-417. doi: 10.1111/cge.13663. Epub 2020 Jan 13. Clin Genet. 2020. PMID: 31674016
Phenotype and genotype spectra of a Chinese cohort with nephronophthisis-related ciliopathy.
Tang X, Liu C, Liu X, Chen J, Fan X, Liu J, Ma D, Cao G, Chen Z, Xu D, Zhu Y, Jiang X, Cheng L, Wu Y, Hou L, Li Y, Shao X, Zheng S, Zhang A, Zheng B, Jian S, Rong Z, Su Q, Gao X, Rao J, Shen Q, Xu H; Chinese Children Genetic Kidney Disease Database (CCGKDD); “Internet Plus” Nephrology Alliance of the National Center for Children’s Care. Tang X, et al. Among authors: zhang a. J Med Genet. 2022 Feb;59(2):147-154. doi: 10.1136/jmedgenet-2020-107184. Epub 2020 Dec 15. J Med Genet. 2022. PMID: 33323469
Multi-centre study of the clinical features and gene variant spectrum of Gitelman syndrome in Chinese children.
Shen Q, Chen J, Yu M, Lin Z, Nan X, Dong B, Fang X, Chen J, Ding G, Zhang A, Gao C, Miao L, Xu Y, Jiang X, Bai H, Zhuang J, Gao X, Xu H; for Chinese Children Genetic Kidney Disease Database (CCGKDD). Shen Q, et al. Among authors: zhang a. Clin Genet. 2021 Apr;99(4):558-564. doi: 10.1111/cge.13913. Epub 2021 Feb 2. Clin Genet. 2021. PMID: 33382082
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