Lu Y - Search Results

1

Clinical features and molecular basis of 102 Chinese patients with congenital dysfibrinogenemia.

Zhou J, Ding Q, Chen Y, Ouyang Q, Jiang L, Dai J, Lu Y, Wu X, Liang Q, Wang H, Wang X. Zhou J, et al. Among authors: lu y. Blood Cells Mol Dis. 2015 Dec;55(4):308-15. doi: 10.1016/j.bcmd.2015.06.002. Epub 2015 Jun 14. Blood Cells Mol Dis. 2015. PMID: 26460252

2

[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. Zhonghua Xue Ye Xue Za Zhi. 2011 Mar;32(3):153-7. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 21535951 Chinese.

3

Molecular basis of type I antithrombin deficiency in two women with recurrent venous thromboembolism in the first trimester of pregnancy.

Xia Y, Lu QY, Lu YL, Dai J, Ding QL, Wang XF, Xi XD, Wang HL. Xia Y, et al. Among authors: lu qy, lu yl. Blood Cells Mol Dis. 2012 Apr 15;48(4):254-9. doi: 10.1016/j.bcmd.2012.02.005. Epub 2012 Mar 15. Blood Cells Mol Dis. 2012. PMID: 22424603

4

[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. Zhonghua Xue Ye Xue Za Zhi. 2012 Jun;33(6):475-9. Zhonghua Xue Ye Xue Za Zhi. 2012. PMID: 22967385 Chinese.

5

[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. 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.

6

Thromboelastography predicts risks of obstetric complication occurrence in (hypo)dysfibrinogenemia patients under non-pregnant state.

Zhou J, Xin Y, Ding Q, Jiang L, Chen Y, Dai J, Lu Y, Wu X, Liang Q, Wang H, Wang X. Zhou J, et al. Among authors: lu y. Clin Exp Pharmacol Physiol. 2016 Feb;43(2):149-56. doi: 10.1111/1440-1681.12509. Clin Exp Pharmacol Physiol. 2016. PMID: 26510121

7

Clinical manifestations and mutation spectrum of 57 subjects with congenital factor XI deficiency in China.

Shao Y, Cao Y, Lu Y, Dai J, Ding Q, Wang X, Xi X, Wang H. Shao Y, et al. Among authors: lu y. Blood Cells Mol Dis. 2016 May;58:29-34. doi: 10.1016/j.bcmd.2016.01.004. Epub 2016 Jan 18. Blood Cells Mol Dis. 2016. PMID: 27067486

8

Dysfibrinogenemia-associated novel heterozygous mutation, Shanghai (FGA c.169_180+2 del), leads to N-terminal truncation of fibrinogen Aα chain and impairs fibrin polymerization.

Zhou J, Ding Q, Wu W, Ouyang Q, Xie Y, Wu X, Lu Y, Dai J, Liang Q, Wang H, Wang X, Hu Y. Zhou J, et al. Among authors: lu y. J Clin Pathol. 2017 Feb;70(2):145-153. doi: 10.1136/jclinpath-2016-203862. Epub 2016 Aug 23. J Clin Pathol. 2017. PMID: 27555433

9

[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. Zhonghua Xue Ye Xue Za Zhi. 2010 Mar;31(3):149-53. Zhonghua Xue Ye Xue Za Zhi. 2010. PMID: 20510101 Chinese.

10

[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. Zhonghua Xue Ye Xue Za Zhi. 2011 Feb;32(2):99-102. Zhonghua Xue Ye Xue Za Zhi. 2011. PMID: 21429375 Chinese.

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