Liu WL - Search Results

1

[The mechanistic rote of KCNH2 gene L413P and L559H mutations in long QT syndrome].

Li CL, Hu DY, Liu WL, Qi SY, Wang HT, Li L, Gong QM, Zhou ZF. Li CL, et al. Among authors: liu wl. Zhonghua Nei Ke Za Zhi. 2007 Oct;46(10):838-41. Zhonghua Nei Ke Za Zhi. 2007. PMID: 18218237 Chinese.

2

[Association between pre-excitation syndrome and 7q3 D7S505 pseudonym gene].

Liu W, Liu G, Hu D, Qi Y, Shan Z, Luo L, Zhang M, Wang L, Yi J. Liu W, et al. Zhonghua Yi Xue Za Zhi. 2002 Jun 25;82(12):820-3. Zhonghua Yi Xue Za Zhi. 2002. PMID: 12126529 Chinese.

3

KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.

Liu W, Yang J, Hu D, Kang C, Li C, Zhang S, Li P, Chen Z, Qin X, Ying K, Li Y, Li Y, Li Z, Cheng X, Li L, Qi Y, Chen S, Wang Q. Liu W, et al. Hum Mutat. 2002 Dec;20(6):475-6. doi: 10.1002/humu.9085. Hum Mutat. 2002. PMID: 12442276 Free PMC article.

4

Familial Wolff-Parkinson-White syndrome is linked to the loci on chromosome 7q3.

Liu W, Liu G, Hu D, Qi Y, Shan Z, Yang D, Liu D, Wang Y. Liu W, et al. Chin Med J (Engl). 2002 Nov;115(11):1733-5. Chin Med J (Engl). 2002. PMID: 12609097

5

Mutation analysis of potassium channel genes KCNQ1 and KCNH2 in patients with long QT syndrome.

Liu W, Hu D, Li C, Li P, Li Y, Li Z, Li L, Qin X, Dong W, Qi Y, Chen S, Wang Q. Liu W, et al. Chin Med J (Engl). 2003 Sep;116(9):1333-5. Chin Med J (Engl). 2003. PMID: 14527360

6

Clinical features and management of congenital long QT syndrome: a report on 54 patients from a national registry.

Li C, Hu D, Qin X, Li Y, Li P, Liu W, Li Z, Li L, Wang L. Li C, et al. Heart Vessels. 2004 Jan;19(1):38-42. doi: 10.1007/s00380-003-0733-9. Heart Vessels. 2004. PMID: 14685754

7

[Spectrum of ST-T-wave changes in hereditary long-QT syndrome in Chinese].

Liu WL, Hu DY, Li ZM, Li CL, Li YT, Qin XG, Li L. Liu WL, et al. Zhonghua Nei Ke Za Zhi. 2004 May;43(5):352-5. Zhonghua Nei Ke Za Zhi. 2004. PMID: 15182506 Chinese.

8

[The mutation scanning of KCNQ1 gene for 31 long QT syndrome families].

Li P, Li CL, Hu DY, Liu WL, Qin XG, Li YT, Li ZM, Li L. Li P, et al. Among authors: liu wl. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Jun;21(3):236-9. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15192825 Chinese.

9

Association of genetic polymorphisms in the fibrinogen and platelet glycoprotein genes with unstable angina in Chinese patients.

Ni Y, Hu D, Yu H, Li C, Liu W, Wang H, Li L. Ni Y, et al. Clin Cardiol. 2004 Aug;27(8):455-8. doi: 10.1002/clc.4960270807. Clin Cardiol. 2004. PMID: 15346842 Free PMC article.

10

[Mutations in beta myosin heavy chain gene: two mutations in Chinese with familial hypertrophic cardiomyopathy and the correlation between the genotype and phenotype].

Xie WL, Liu WL, Hu DY, Cui W, Zhu TG, Li CL, Sun YH, Li L, Li TC, Bian H, Tong QG. Xie WL, et al. Among authors: liu wl. Zhonghua Yi Xue Za Zhi. 2004 Oct 2;84(19):1610-3. Zhonghua Yi Xue Za Zhi. 2004. PMID: 15569455 Chinese.

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