Zhang W - Search Results

1

Prevalence and spectrum of GATA5 mutations associated with congenital heart disease.

Jiang JQ, Li RG, Wang J, Liu XY, Xu YJ, Fang WY, Chen XZ, Zhang W, Wang XZ, Yang YQ. Jiang JQ, et al. Among authors: zhang w. Int J Cardiol. 2013 May 25;165(3):570-3. doi: 10.1016/j.ijcard.2012.09.039. Epub 2012 Sep 30. Int J Cardiol. 2013. PMID: 23031282 No abstract available.

2

A novel GATA4 loss-of-function mutation associated with congenital ventricular septal defect.

Yang YQ, Li L, Wang J, Liu XY, Chen XZ, Zhang W, Wang XZ, Jiang JQ, Liu X, Fang WY. Yang YQ, et al. Among authors: zhang w. Pediatr Cardiol. 2012 Apr;33(4):539-46. doi: 10.1007/s00246-011-0146-y. Epub 2011 Nov 20. Pediatr Cardiol. 2012. PMID: 22101736

3

Novel GATA4 mutations in patients with congenital ventricular septal defects.

Yang YQ, Wang J, Liu XY, Chen XZ, Zhang W, Wang XZ, Liu X, Fang WY. Yang YQ, et al. Among authors: zhang w. Med Sci Monit. 2012 Jun;18(6):CR344-50. doi: 10.12659/msm.882877. Med Sci Monit. 2012. PMID: 22648249 Free PMC article.

4

PITX2c loss-of-function mutations responsible for congenital atrial septal defects.

Yuan F, Zhao L, Wang J, Zhang W, Li X, Qiu XB, Li RG, Xu YJ, Xu L, Qu XK, Fang WY, Yang YQ. Yuan F, et al. Among authors: zhang w. Int J Med Sci. 2013 Aug 22;10(10):1422-9. doi: 10.7150/ijms.6809. eCollection 2013. Int J Med Sci. 2013. PMID: 23983605 Free PMC article.

5

Novel NKX2-5 mutations in patients with familial atrial septal defects.

Liu XY, Wang J, Yang YQ, Zhang YY, Chen XZ, Zhang W, Wang XZ, Zheng JH, Chen YH. Liu XY, et al. Among authors: zhang w, zhang yy. Pediatr Cardiol. 2011 Feb;32(2):193-201. doi: 10.1007/s00246-010-9859-6. Epub 2010 Dec 25. Pediatr Cardiol. 2011. PMID: 21188375

6

Mutation spectrum of GATA4 associated with congenital atrial septal defects.

Yang YQ, Wang J, Liu XY, Chen XZ, Zhang W, Wang XZ. Yang YQ, et al. Among authors: zhang w. Arch Med Sci. 2013 Dec 30;9(6):976-83. doi: 10.5114/aoms.2013.39788. Epub 2013 Dec 26. Arch Med Sci. 2013. PMID: 24482639 Free PMC article.

7

TBX1 loss-of-function mutation contributes to congenital conotruncal defects.

Zhang M, Li FX, Liu XY, Hou JY, Ni SH, Wang J, Zhao CM, Zhang W, Kong Y, Huang RT, Xue S, Yang YQ. Zhang M, et al. Among authors: zhang w. Exp Ther Med. 2018 Jan;15(1):447-453. doi: 10.3892/etm.2017.5362. Epub 2017 Oct 24. Exp Ther Med. 2018. PMID: 29250159 Free PMC article.

8

[Transcatheter closure of paraprosthetic valve leaks post surgical valve replacements].

Pan X, Zhang W, Wu WH, Lu J, Wang C, Feng Y, Fang WY. Pan X, et al. Among authors: zhang w. Zhonghua Xin Xue Guan Bing Za Zhi. 2011 Mar;39(3):217-20. Zhonghua Xin Xue Guan Bing Za Zhi. 2011. PMID: 21609525 Chinese.

9

Multiple aortico-cameral tunnels associated with bicuspid aortic valve in aged: a case report.

Qiu XB, Shi HY, Liu L, Chen H, Wu WH, Qiu ZK, Zhang W, Fang WY. Qiu XB, et al. Among authors: zhang w. Chin Med J (Engl). 2009 Sep 20;122(18):2184-5. Chin Med J (Engl). 2009. PMID: 19781308 No abstract available.

10

Left and right atrial size and the occurrence predictors in patients with paroxysmal atrial fibrillation.

Cui Q, Zhang W, Wang H, Sun X, Yang H, Meng X, Zhang Y, Wang H. Cui Q, et al. Among authors: zhang w, zhang y. Int J Cardiol. 2008 Oct 30;130(1):69-71. doi: 10.1016/j.ijcard.2007.07.006. Epub 2007 Aug 10. Int J Cardiol. 2008. PMID: 17692946

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

87,576 results

Search Page

Filters