Li J - Search Results

1

[Study on novel mutations of MEF2A gene in Chinese patients with coronary artery disease].

Li J, Yang JG, Li W, Du R, Gui L, Tian L, Guo QH. Li J, et al. Among authors: li w. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Jun;23(3):265-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16767660 Chinese.

2

[Gene mutation in secundum atrial septal defect: analysis of a Chinese family with 3 patients].

Tian L, Zhu JF, Yang JG, Zhu QH, Du R, Li J, Li W. Tian L, et al. Among authors: li j, li w. Zhonghua Yi Xue Za Zhi. 2008 Jan 22;88(4):250-3. Zhonghua Yi Xue Za Zhi. 2008. PMID: 18361836 Chinese.

3

[Relationship between congenital long QT syndrome and Brugada syndrome gene mutation].

Du R, Ren FX, Yang JG, Yuan GH, Zhang SY, Kang CL, Li W, Gui L, Li J. Du R, et al. Among authors: li j, li w. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005 Jun;27(3):289-94. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005. PMID: 16038262 Chinese.

4

Effects of telmisartan on paroxysmal atrial fibrillation in hypertensive patients.

Li J, Chen H, Zhou Q, Hu L, Ma L, Han H, Li W, Du R, Tian L. Li J, et al. Among authors: li w. Pak J Pharm Sci. 2017 Sep;30(5):1651-1655. Pak J Pharm Sci. 2017. PMID: 29084686 Clinical Trial.

5

Inhibitory effect of rhynchophylline on human ether-a-go-go related gene channel.

Gui L, Li ZW, Du R, Yuan GH, Li W, Ren FX, Li J, Yang JG. Gui L, et al. Among authors: li zw, li j, li w. Sheng Li Xue Bao. 2005 Oct 25;57(5):648-52. Sheng Li Xue Bao. 2005. PMID: 16220205 Free article.

6

[Mutation analysis of GCH1 gene in Chinese patients with dopa responsive dystonia].

Li J, Tang BS, Guo JF, Zhang YH, Xie ZG, Yan XX, Shen L, Jiang H, Zhang XW, Xia K, Pan Q. Li J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Jun;24(3):302-4. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007. PMID: 17557242 Chinese.

7

[Mutation analysis of the PAX6 gene in a family with congenital aniridia and cataract].

Lin Y, Li J, Yang Y, Yang JY, Zhang B, Tang X, Liu XQ, Lu F, Yang ZL. Lin Y, et al. Among authors: li j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):542-5. doi: 10.3760/cma.j.issn.1003-9406.2009.05.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19806578 Chinese.

8

[Linkage analysis of a Chinese family with autosomal dominant congenital retinaochoroidal coloboma].

Dong JM, Bu J, Li J, Zhuo YL, Wang LJ. Dong JM, et al. Among authors: li j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Jun;26(3):263-6. doi: 10.3760/cma.j.issn.1003-9406.2009.03.006. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19504436 Chinese.

9

Identification of novel mutations in Chinese Hans with autosomal dominant polycystic kidney disease.

Yu C, Yang Y, Zou L, Hu Z, Li J, Liu Y, Ma Y, Ma M, Su D, Zhang S. Yu C, et al. Among authors: li j. BMC Med Genet. 2011 Dec 20;12:164. doi: 10.1186/1471-2350-12-164. BMC Med Genet. 2011. PMID: 22185115 Free PMC article.

10

[Identification of a novel PHOX2A gene mutation in a Chinese family with congenital fibrosis of extraocular muscles type 2].

Dong JM, Shen Q, Li J, Du W, Pang HL, Lin SF, Bu J. Dong JM, et al. Among authors: li j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Feb;29(1):5-8. doi: 10.3760/cma.j.issn.1003-9406.2012.01.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 22311481 Chinese.

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