Shu K - Search Results

1

[Analysis of a pedigree affected with congenital dysfibrinogenemia due to a novel Gly31Glu mutation of FGA gene].

Wang X, Yang X, Yang W, Shu K, Li F, Liu J, Zhang Z, Li S, Jiang M. Wang X, et al. Among authors: shu k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Sep 10;36(9):901-904. doi: 10.3760/cma.j.issn.1003-9406.2019.09.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31515786 Chinese.

2

[Clinical and genetic analysis of 8 Chinese pedigrees with inherited dysfibrinogenemia].

Jiang M, Wang X, Shu K, Jiang W, Huang Y, Lin Y, Li S, Hu Y. Jiang M, et al. Among authors: shu k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Apr;31(2):134-9. doi: 10.3760/cma.j.issn.1003-9406.2014.02.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 24711018 Chinese.

3

[Analysis on the novel compound heterozygous mutation FⅪ of a patient with hereditary factor Ⅺ deficiency].

Xu K, Shu KY, Li FF, Chen T, Liu J, Jin SS, Guo JJ, Zhang ZH, Jiang MH. Xu K, et al. Among authors: shu ky. Zhonghua Yi Xue Za Zhi. 2017 Dec 26;97(48):3774-3778. doi: 10.3760/cma.j.issn.0376-2491.2017.48.004. Zhonghua Yi Xue Za Zhi. 2017. PMID: 29325334 Chinese.

4

The analysis of false prolongation of the activated partial thromboplastin time (activator: silica): Interference of C-reactive protein.

Liu J, Li F, Shu K, Chen T, Wang X, Xie Y, Li S, Zhang Z, Jin S, Jiang M. Liu J, et al. Among authors: shu k. J Clin Lab Anal. 2018 Oct;32(8):e22571. doi: 10.1002/jcla.22571. Epub 2018 May 13. J Clin Lab Anal. 2018. PMID: 29756266 Free PMC article.

5

[Identification of compound heterozygous mutations p.Gly400Val and p.Arg532Ter of the F11 gene in a Chinese patient with hereditary factor XI deficiency].

Shu K, Xu K, Li F, Chen T, Liu J, Jin S, Guo J, Zhang Z, Jiang M. Shu K, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Aug 10;35(4):522-526. doi: 10.3760/cma.j.issn.1003-9406.2018.04.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30098248 Chinese.

6

[Genotypic and phenotypic analysis of a case with inherited coagulation factor X deficiency].

Chen T, Li F, Shu K, Liu J, Shen C, Zhang Z, Jin S, Wang X, Jiang M. Chen T, et al. Among authors: shu k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Aug 10;35(4):544-547. doi: 10.3760/cma.j.issn.1003-9406.2018.04.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30098253 Chinese.

7

[Phenotype and gene analysis of a hereditary coagulation factor Ⅻ deficiency].

Li SS, Liu J, Shen CF, Shu KY, Wang XO, Li FF, Yang X, Yang W, Wang JL, Jiang MH. Li SS, et al. Among authors: shu ky. Zhonghua Xue Ye Xue Za Zhi. 2018 Aug 14;39(8):679-681. doi: 10.3760/cma.j.issn.0253-2727.2018.08.014. Zhonghua Xue Ye Xue Za Zhi. 2018. PMID: 30180472 Free PMC article. Chinese. No abstract available.

8

[Phenotypic and genetic analysis of two pedigrees affected with hereditary coagulation FXII deficiency].

Li S, Shen C, Shu K, Liu J, Wang X, Li F, Yang X, Zhang Z, Chen B, Jiang M. Li S, et al. Among authors: shu k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Dec 10;35(6):800-803. doi: 10.3760/cma.j.issn.1003-9406.2018.06.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30512149 Chinese.

9

Acquired Factor V Inhibitor with Symptoms and Titer of Inhibitor Differences: Report of Two Cases.

Li F, Shu K, Liu J, Shen C, Wang X, Zhang Z, Jiang M. Li F, et al. Among authors: shu k. Acta Haematol. 2019;141(3):148-150. doi: 10.1159/000496080. Epub 2019 Feb 15. Acta Haematol. 2019. PMID: 30783058 Free article. No abstract available.

10

[Clinical and genotypic analysis of two Chinese pedigrees affected with hereditary coagulable factor VII deficiency].

Li F, Liu J, Zhu Q, Shen C, Shu K, Yang X, Yang W, Lin S, Chen B, Jiang M. Li F, et al. Among authors: shu k. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Mar 10;36(3):221-224. doi: 10.3760/cma.j.issn.1003-9406.2019.03.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30835350 Chinese.

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