Zhang LW - Search Results

1

[Analysis of phenotype and genotype in four Chinese pedigrees with inherited coagulation factor V deficiency.].

Huang DD, Wang XF, Chen HY, Xu GQ, Zhang LW, Dai J, Lu YL, Ding QL, Xi XD, Wang HL. Huang DD, et al. Among authors: zhang lw. Zhonghua Xue Ye Xue Za Zhi. 2010 Mar;31(3):149-53. Zhonghua Xue Ye Xue Za Zhi. 2010. PMID: 20510101 Chinese.

2

[Identification of genetic defects in a Chinese pedigree with factor XIII deficiency: case report and literature review].

Xu G, Liang Q, Zhang L, Shen Y, Ding Q, Wang X, Wang H. Xu G, et al. Zhonghua Xue Ye Xue Za Zhi. 2015 Oct;36(10):844-8. doi: 10.3760/cma.j.issn.0253-2727.2015.10.008. Zhonghua Xue Ye Xue Za Zhi. 2015. PMID: 26477763 Free PMC article. Review. Chinese.

3

[The application of thrombin generation tests to warfarin anticoagulation monitoring].

Chen HY, Ding QL, Zhang LW, Xu GQ, Dai J, Wang XF, Xi XD, Wang HL. Chen HY, et al. Among authors: zhang lw. Zhonghua Xue Ye Xue Za Zhi. 2008 Mar;29(3):168-70. Zhonghua Xue Ye Xue Za Zhi. 2008. PMID: 18788615 Chinese.

4

[Phenotype and genotype analysis of three Chinese pedigrees with von Willebrand disease].

Qin HH, Wang XF, Ding QL, Xu GQ, Zhang LW, Dai J, Lu YL, Xi XD, Wang HL. Qin HH, et al. Among authors: zhang lw. Zhonghua Xue Ye Xue Za Zhi. 2011 Feb;32(2):99-102. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 21429375 Chinese.

5

[Analysis of phenotype and genotype in three Chinese pedigrees with inherited dysfibrinogenemia].

Ouyang Q, Ding QL, Huang DD, Xu GQ, Zhang LW, Dai J, Lu YL, Wang XF, Xi XD, Wang HL. Ouyang Q, et al. Among authors: zhang lw. Zhonghua Xue Ye Xue Za Zhi. 2011 Mar;32(3):153-7. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 21535951 Chinese.

6

[Molecular mechanisms of recurrent venous thrombosis in two pedigrees with type I antithrombin deficiency].

Xia Y, Ding QL, Xu GQ, Zhang LW, Dai J, Lu YL, Wang XF, Xi XD, Wang HL. Xia Y, et al. Among authors: zhang lw. Zhonghua Xue Ye Xue Za Zhi. 2011 Dec;32(12):848-53. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 22339960 Chinese.

7

[Genotype and function analyses of four inherited dysfibrinogenemia pedigree caused by Arg16 amino acid substitution in fibrinogen Aα chain].

Jiang LL, Wang XF, Ding QL, Xu GQ, Zhang LW, Dai J, Lu YL, Xi XD, Wang HL. Jiang LL, et al. Among authors: zhang lw. Zhonghua Xue Ye Xue Za Zhi. 2012 Jun;33(6):475-9. Zhonghua Xue Ye Xue Za Zhi. 2012. PMID: 22967385 Chinese.

8

[Phenotype and genotype analysis of two Chinese pedigrees with type 3 von Willebrand diseases].

Jiang LL, Wang XF, Ding QL, Xu GQ, Zhang LW, Dai J, Lu YL, Wang HL, Xi XD. Jiang LL, et al. Among authors: zhang lw. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Oct;29(5):524-8. doi: 10.3760/cma.j.issn.1003-9406.2012.05.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23042386 Chinese.

9

[The phenotypic and genotypic diagnosis of three Chinese patients with von Willebrand disease].

Jiang LL, Cao YN, Wang XF, Ding QL, Xu GQ, Zhang LW, Dai J, Lu YL, Wang HL, Xi XD. Jiang LL, et al. Among authors: zhang lw. Zhonghua Nei Ke Za Zhi. 2012 Oct;51(10):788-92. Zhonghua Nei Ke Za Zhi. 2012. PMID: 23290978 Chinese.

10

[Functional study of abnormal fibrinogen caused by Arg275His mutation in fibrinogen γ chain].

Zhou JY, Wang XF, Ding QL, Xu GQ, Zhang LW, Dai J, Lu YL, Xi XD, Wang HL. Zhou JY, et al. Among authors: zhang lw. Zhonghua Xue Ye Xue Za Zhi. 2013 Mar;34(3):190-4. doi: 10.3760/cma.j.issn.0253-2727.2013.03.002. Zhonghua Xue Ye Xue Za Zhi. 2013. PMID: 23683413 Chinese.

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