Zou Y - Search Results

1

Malignant effects of multiple rare variants in sarcomere genes on the prognosis of patients with hypertrophic cardiomyopathy.

Wang J, Wang Y, Zou Y, Sun K, Wang Z, Ding H, Yuan J, Wei W, Hou Q, Wang H, Liu X, Zhang H, Ji Y, Zhou X, Sharma RK, Wang D, Ahmad F, Hui R, Song L. Wang J, et al. Among authors: zou y. Eur J Heart Fail. 2014 Sep;16(9):950-7. doi: 10.1002/ejhf.144. Epub 2014 Jul 31. Eur J Heart Fail. 2014. PMID: 25132132 Free article.

2

Prevalence of idiopathic hypertrophic cardiomyopathy in China: a population-based echocardiographic analysis of 8080 adults.

Zou Y, Song L, Wang Z, Ma A, Liu T, Gu H, Lu S, Wu P, Zhang dagger Y, Shen dagger L, Cai Y, Zhen double dagger Y, Liu Y, Hui R. Zou Y, et al. Am J Med. 2004 Jan 1;116(1):14-8. doi: 10.1016/j.amjmed.2003.05.009. Am J Med. 2004. PMID: 14706660

3

[Clinical and genetic characteristics of a Chinese family of primary pulmonary hypertension].

Jing ZC, Lu LH, Zou YB, You SJ, Han ZY, Zhang Q, Yang YJ, Hui RT, Cheng XS. Jing ZC, et al. Zhonghua Yi Xue Za Zhi. 2004 Feb 2;84(3):199-202. Zhonghua Yi Xue Za Zhi. 2004. PMID: 15059534 Chinese.

4

Mutations profile in Chinese patients with hypertrophic cardiomyopathy.

Song L, Zou Y, Wang J, Wang Z, Zhen Y, Lou K, Zhang Q, Wang X, Wang H, Li J, Hui R. Song L, et al. Among authors: zou y. Clin Chim Acta. 2005 Jan;351(1-2):209-16. doi: 10.1016/j.cccn.2004.09.016. Clin Chim Acta. 2005. PMID: 15563892

5

MYBPC3 polymorphism is a modifier for expression of cardiac hypertrophy in patients with hypertrophic cardiomyopathy.

Wang P, Zou Y, Fu C, Zhou X, Hui R. Wang P, et al. Among authors: zou y. Biochem Biophys Res Commun. 2005 Apr 8;329(2):796-9. doi: 10.1016/j.bbrc.2005.02.004. Biochem Biophys Res Commun. 2005. PMID: 15737656 Clinical Trial.

6

[A novel LMNA gene mutation E82K associated with familial dilated cardiomyopathy].

Wang H, Zheng WY, Wang JZ, Wang XJ, Zhen YS, Song L, Zou YB, Hui RT. Wang H, et al. Zhonghua Xin Xue Guan Bing Za Zhi. 2005 Oct;33(10):875-9. Zhonghua Xin Xue Guan Bing Za Zhi. 2005. PMID: 16266469 Chinese.

7

Mutation Glu82Lys in lamin A/C gene is associated with cardiomyopathy and conduction defect.

Wang H, Wang J, Zheng W, Wang X, Wang S, Song L, Zou Y, Yao Y, Hui R. Wang H, et al. Among authors: zou y. Biochem Biophys Res Commun. 2006 May 26;344(1):17-24. doi: 10.1016/j.bbrc.2006.03.149. Biochem Biophys Res Commun. 2006. PMID: 16630578

8

[Familiar hypertrophic cardiomyopathy caused by a IVS15-1G > A mutation in cardiac myosin-binding protein C gene].

Zou YB, Wang JZ, Wu GR, Song L, Wang SX, Yu H, Zhang Q, Wang H, Hui RT. Zou YB, et al. Zhonghua Xin Xue Guan Bing Za Zhi. 2006 Aug;34(8):699-702. Zhonghua Xin Xue Guan Bing Za Zhi. 2006. PMID: 17081393 Chinese.

9

[Clinical features of dilated cardiomyopathy-like hypertrophic cardiomyopathy caused by a 13261 G > A mutation in cardiac myosin-binding protein C gene].

Wang SX, Zou YB, Fu CY, Wang H, Wang JZ, Song XD, Chen JZ, Hui RT. Wang SX, et al. Zhonghua Xin Xue Guan Bing Za Zhi. 2007 Jan;35(1):17-20. Zhonghua Xin Xue Guan Bing Za Zhi. 2007. PMID: 17386157 Chinese.

10

[Family hypertrophic cardiomyopathy caused by a 14035c > t mutation in cardiac troponin T gene].

Wang SX, Zou YB, Fu CY, Song L, Wang H, Wang JZ, Song XD, Chen JZ, Hui RT. Wang SX, et al. Zhonghua Yi Xue Za Zhi. 2007 Feb 6;87(6):371-4. Zhonghua Yi Xue Za Zhi. 2007. PMID: 17456375 Chinese.

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