Xu K - Search Results

1

Incidence and cost of haemolytic uraemic syndrome in urban China: a national population-based analysis.

Feng J, Xu K, Shi X, Xu L, Liu L, Wang F, Zhong X, Liu G, Wang J, Gao P, Ding J, Wang S, Zhan S. Feng J, et al. Among authors: xu k, xu l. BMC Nephrol. 2022 Mar 30;23(1):122. doi: 10.1186/s12882-022-02746-2. BMC Nephrol. 2022. PMID: 35354386 Free PMC article.

2

Spectrum of thrombotic complications and their outcomes in Chinese children with primary nephrotic syndrome.

Lv YL, Guan N, Ding J, Yao Y, Xiao HJ, Zhong XH, Wang F, Liu XY, Zhang HW, Su BG, Xu K. Lv YL, et al. Among authors: xu k. Ital J Pediatr. 2020 Dec 9;46(1):182. doi: 10.1186/s13052-020-00942-0. Ital J Pediatr. 2020. PMID: 33298123 Free PMC article.

3

Spectrum of Mutations in Pediatric Non-glomerular Chronic Kidney Disease Stages 2-5.

Wang X, Xiao H, Yao Y, Xu K, Liu X, Su B, Zhang H, Guan N, Zhong X, Zhang Y, Ding J, Wang F. Wang X, et al. Among authors: xu k. Front Genet. 2021 Jul 6;12:697085. doi: 10.3389/fgene.2021.697085. eCollection 2021. Front Genet. 2021. PMID: 34295353 Free PMC article.

4

Interpretation of Autosomal Recessive Kidney Diseases With "Presumed Homozygous" Pathogenic Variants Should Consider Technical Pitfalls.

Deng H, Zhang Y, Yao Y, Xiao H, Su B, Xu K, Guan N, Ding J, Wang F. Deng H, et al. Among authors: xu k. Front Pediatr. 2020 Apr 17;8:165. doi: 10.3389/fped.2020.00165. eCollection 2020. Front Pediatr. 2020. PMID: 32363171 Free PMC article.

5

[A child with diffuse mesangial sclerosis caused by a missense mutation of TRPC6 gene].

Xu K, Yin M, Xiao H, Wang S, Liu L, Wang F. Xu K, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022 Mar 10;39(3):325-329. doi: 10.3760/cma.j.cn511374-20201211-00868. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2022. PMID: 35315046 Chinese.

6

Genetic and Functional Evidence Supports LPAR1 as a Susceptibility Gene for Hypertension.

Xu K, Ma L, Li Y, Wang F, Zheng GY, Sun Z, Jiang F, Chen Y, Liu H, Dang A, Chen X, Chun J, Tian XL. Xu K, et al. Hypertension. 2015 Sep;66(3):641-6. doi: 10.1161/HYPERTENSIONAHA.115.05515. Epub 2015 Jun 29. Hypertension. 2015. PMID: 26123684

7

Comprehensive Genetic Analysis Unraveled the Missing Heritability in a Chinese Cohort With Wolfram Syndrome 1: Clinical and Genetic Findings.

Zhang X, Xie Y, Xu K, Chang H, Zhang X, Li Y. Zhang X, et al. Among authors: xu k. Invest Ophthalmol Vis Sci. 2022 Sep 1;63(10):9. doi: 10.1167/iovs.63.10.9. Invest Ophthalmol Vis Sci. 2022. PMID: 36098976 Free PMC article.

8

Potential Alterations of Functional Connectivity Analysis in the Patients with Chronic Prostatitis/Chronic Pelvic Pain Syndrome.

Ge S, Hu Q, Guo Y, Xu K, Xia G, Sun C. Ge S, et al. Among authors: xu k. Neural Plast. 2021 May 7;2021:6690414. doi: 10.1155/2021/6690414. eCollection 2021. Neural Plast. 2021. PMID: 34035803 Free PMC article.

9

Doxazosin gastrointestinal therapeutic system versus tamsulosin for the treatment of benign prostatic hyperplasia: a study in Chinese patients.

Xue Z, Zhang Y, Ding Q, He Z, Wang J, Xu K. Xue Z, et al. Among authors: xu k. Int J Urol. 2007 Feb;14(2):118-22. doi: 10.1111/j.1442-2042.2007.01502.x. Int J Urol. 2007. PMID: 17302567 Clinical Trial.

10

Are EORTC risk tables suitable for Chinese patients with non-muscle-invasive bladder cancer?

Ding W, Chen Z, Gou Y, Sun C, Xu K, Tan J, Tong S, Xia G, Ding Q. Ding W, et al. Among authors: xu k. Cancer Epidemiol. 2014 Apr;38(2):157-61. doi: 10.1016/j.canep.2014.02.001. Epub 2014 Mar 11. Cancer Epidemiol. 2014. PMID: 24629527

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