Zhang W - Search Results

1

[Association of single nucleotide polymorphism of megsin gene with IgA nephropathy].

Wang ZH, Chen N, Pan XX, Ren H, Wang WM, Zhang W, Hao CL, Zhu J, Lu Y, Han B. Wang ZH, et al. Among authors: zhang w. Zhonghua Yi Xue Za Zhi. 2006 May 23;86(19):1337-41. Zhonghua Yi Xue Za Zhi. 2006. PMID: 16796905 Chinese.

2

Predicting progression of IgA nephropathy: new clinical progression risk score.

Xie J, Kiryluk K, Wang W, Wang Z, Guo S, Shen P, Ren H, Pan X, Chen X, Zhang W, Li X, Shi H, Li Y, Gharavi AG, Chen N. Xie J, et al. Among authors: zhang w. PLoS One. 2012;7(6):e38904. doi: 10.1371/journal.pone.0038904. Epub 2012 Jun 14. PLoS One. 2012. PMID: 22719981 Free PMC article.

3

IgA Nephropathy Susceptibility Loci and Disease Progression.

Shi M, Ouyang Y, Yang M, Yang M, Zhang X, Huang W, Wang W, Wang Z, Zhang W, Chen X, Pan X, Ren H, Chen N, Xie J. Shi M, et al. Among authors: zhang w, zhang x. Clin J Am Soc Nephrol. 2018 Sep 7;13(9):1330-1338. doi: 10.2215/CJN.13701217. Epub 2018 Jul 24. Clin J Am Soc Nephrol. 2018. PMID: 30042224 Free PMC article.

4

Detection of COL4A5 gene mutations in Chinese patients with Alport's syndrome.

Pan X, Yan J, Ren H, Zhang W, Shi H, Yu H, Wang C, Hao C, Chen X, Chen N. Pan X, et al. Among authors: zhang w. Nephrol Dial Transplant. 2004 May;19(5):1123-8. doi: 10.1093/ndt/gfh099. Epub 2004 Feb 19. Nephrol Dial Transplant. 2004. PMID: 14993485

5

Effect of MDR1 gene polymorphism on progression of end-stage renal disease.

Zhang WX, Chen B, Zhang W, Chen N, Yu ZC, Cai WM. Zhang WX, et al. Among authors: zhang w. Acta Pharmacol Sin. 2007 Apr;28(4):579-83. doi: 10.1111/j.1745-7254.2007.00517.x. Acta Pharmacol Sin. 2007. PMID: 17376299

6

Propylthiouracil-associated antineutrophil cytoplasmic autoantibody-positive vasculitis: retrospective study of 19 cases.

Chen YX, Yu HJ, Ni LY, Zhang W, Xu YW, Ren H, Chen XN, Wang XL, Li X, Pan XX, Wang WM, Chen N. Chen YX, et al. Among authors: zhang w. J Rheumatol. 2007 Dec;34(12):2451-6. Epub 2007 Nov 1. J Rheumatol. 2007. PMID: 17985400

7

Novel SLC12A3 mutations in Chinese patients with Gitelman's syndrome.

Shao L, Ren H, Wang W, Zhang W, Feng X, Li X, Chen N. Shao L, et al. Among authors: zhang w. Nephron Physiol. 2008;108(3):p29-36. doi: 10.1159/000117815. Epub 2008 Feb 21. Nephron Physiol. 2008. PMID: 18287808

8

Identification and functional analysis of a novel TRPC6 mutation associated with late onset familial focal segmental glomerulosclerosis in Chinese patients.

Zhu B, Chen N, Wang ZH, Pan XX, Ren H, Zhang W, Wang WM. Zhu B, et al. Among authors: zhang w. Mutat Res. 2009 May 12;664(1-2):84-90. doi: 10.1016/j.mrfmmm.2008.11.021. Epub 2008 Dec 13. Mutat Res. 2009. PMID: 19124028

9

Identification of five novel variants in the thiazide-sensitive NaCl co-transporter gene in Chinese patients with Gitelman syndrome.

Qin L, Shao L, Ren H, Wang W, Pan X, Zhang W, Wang Z, Shen P, Chen N. Qin L, et al. Among authors: zhang w. Nephrology (Carlton). 2009 Feb;14(1):52-8. doi: 10.1111/j.1440-1797.2008.01042.x. Epub 2009 Jan 21. Nephrology (Carlton). 2009. PMID: 19207868

10

Clinicopathological characteristics and outcome of Chinese patients with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: a 9-year retrospective study.

Zhang W, Shi H, Ren H, Shen PY, Pan XX, Li X, Chen YX, Xu YW, Chen XN, Zhu P, Chen N. Zhang W, et al. Nephron Clin Pract. 2009;112(3):c177-83. doi: 10.1159/000218106. Epub 2009 May 13. Nephron Clin Pract. 2009. PMID: 19439988

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