Shi HY - Search Results

1

MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy.

Yuan F, Qiu ZH, Wang XH, Sun YM, Wang J, Li RG, Liu H, Zhang M, Shi HY, Zhao L, Jiang WF, Liu X, Qiu XB, Qu XK, Yang YQ. Yuan F, et al. Among authors: shi hy. Clin Chem Lab Med. 2018 Feb 23;56(3):502-511. doi: 10.1515/cclm-2017-0461. Clin Chem Lab Med. 2018. PMID: 28902616

2

Transcatheter coil embolization of multiple coronary artery-to-left ventricle fistulas: report of a rare case.

Li RG, Fang WY, Shi HY, Qu XK, Chen H, Qiu XB, Xu YJ, Dong JL, Guan SF, Jiang B, Wu WH. Li RG, et al. Among authors: shi hy. Chin Med J (Engl). 2008 Jul 20;121(14):1342-4. Chin Med J (Engl). 2008. PMID: 18713560 No abstract available.

3

Percutaneous repair of inadvertent subclavian artery cannulation: a case report.

Shi HY, Qiu XB, Chen H, Liu ZG, Ye Y, Fang WY. Shi HY, et al. Chin Med J (Engl). 2009 May 5;122(9):1117-8. Chin Med J (Engl). 2009. PMID: 19493453 No abstract available.

4

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: shi hy. Chin Med J (Engl). 2009 Sep 20;122(18):2184-5. Chin Med J (Engl). 2009. PMID: 19781308 No abstract available.

5

Spontaneous resolution of iatrogenic coronary artery to right ventricular fistula secondary to percutaneous coronary intervention.

Qiu XB, Liu L, Hou XM, Han WZ, Ye Y, Dai JJ, Shi HY, Fang WY. Qiu XB, et al. Among authors: shi hy. Chin Med J (Engl). 2013;126(11):2195-6. Chin Med J (Engl). 2013. PMID: 23769583 No abstract available.

6

TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy.

Zhang XL, Qiu XB, Yuan F, Wang J, Zhao CM, Li RG, Xu L, Xu YJ, Shi HY, Hou XM, Qu XK, Xu YW, Yang YQ. Zhang XL, et al. Among authors: shi hy. Biochem Biophys Res Commun. 2015 Mar 27;459(1):166-71. doi: 10.1016/j.bbrc.2015.02.094. Epub 2015 Feb 26. Biochem Biophys Res Commun. 2015. PMID: 25725155 Free article.

7

A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease.

Pan Y, Wang ZG, Liu XY, Zhao H, Zhou N, Zheng GF, Qiu XB, Li RG, Yuan F, Shi HY, Hou XM, Yang YQ. Pan Y, et al. Among authors: shi hy. Pediatr Cardiol. 2015 Oct;36(7):1400-10. doi: 10.1007/s00246-015-1173-x. Epub 2015 Apr 10. Pediatr Cardiol. 2015. PMID: 25860641

8

A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.

Sun YM, Wang J, Qiu XB, Yuan F, Li RG, Xu YJ, Qu XK, Shi HY, Hou XM, Huang RT, Xue S, Yang YQ. Sun YM, et al. Among authors: shi hy. G3 (Bethesda). 2016 Apr 7;6(4):987-92. doi: 10.1534/g3.115.026518. G3 (Bethesda). 2016. PMID: 26865696 Free PMC article.

9

TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome.

Guo DF, Li RG, Yuan F, Shi HY, Hou XM, Qu XK, Xu YJ, Zhang M, Liu X, Jiang JQ, Yang YQ, Qiu XB. Guo DF, et al. Among authors: shi hy. Mol Med Rep. 2016 May;13(5):4349-56. doi: 10.3892/mmr.2016.5043. Epub 2016 Mar 24. Mol Med Rep. 2016. PMID: 27035640 Clinical Trial.

10

CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy.

Qiu XB, Qu XK, Li RG, Liu H, Xu YJ, Zhang M, Shi HY, Hou XM, Liu X, Yuan F, Sun YM, Wang J, Huang RT, Xue S, Yang YQ. Qiu XB, et al. Among authors: shi hy. Clin Chem Lab Med. 2017 Aug 28;55(9):1417-1425. doi: 10.1515/cclm-2016-0612. Clin Chem Lab Med. 2017. PMID: 28099117

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