Yan J - Search Results

1

Dysfibrinogenemia in a patient undergoing artificial abortion after misdiagnosis and review of the literature.

Yan J, Deng D, Luo M, Cheng P, Chi B, Yuan Y, Liao L, Lin F. Yan J, et al. Clin Chim Acta. 2015 Jul 20;447:86-9. doi: 10.1016/j.cca.2015.06.002. Epub 2015 Jun 6. Clin Chim Acta. 2015. PMID: 26057201

2

Lack of association between leptin G-2548A polymorphisms and obesity risk: Evidence based on a meta-analysis.

Yan J, Wang X, Tao H, Yang W, Luo M, Lin F. Yan J, et al. Obes Res Clin Pract. 2015 Jul-Aug;9(4):389-97. doi: 10.1016/j.orcp.2015.01.002. Epub 2015 Feb 27. Obes Res Clin Pract. 2015. PMID: 25733497

3

Meta-Analysis of the Relationship between XRCC1-Arg399Gln and Arg280His Polymorphisms and the Risk of Prostate Cancer.

Yan J, Wang X, Tao H, Deng Z, Yang W, Lin F. Yan J, et al. Sci Rep. 2015 Apr 30;5:9905. doi: 10.1038/srep09905. Sci Rep. 2015. PMID: 25927275 Free PMC article.

4

[Analysis of a family with congenital dysfibrinogenemia caused by an Arg275His mutation in the gamma chain of fibrinogen].

Yan J, Deng D, Deng X, Luo M, Cheng P, Liao L, Lin F. Yan J, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Apr;33(2):160-3. doi: 10.3760/cma.j.issn.1003-9406.2016.02.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27060305 Chinese.

5

Three cases of congenital dysfibrinogenemia in unrelated Chinese families: heterozygous missense mutation in fibrinogen alpha chain Argl6His.

Luo M, Deng D, Xiang L, Cheng P, Liao L, Deng X, Yan J, Lin F. Luo M, et al. Among authors: yan j. Medicine (Baltimore). 2016 Sep;95(39):e4864. doi: 10.1097/MD.0000000000004864. Medicine (Baltimore). 2016. PMID: 27684817 Free PMC article.

6

A novel mutation in the fibrinogen Aα chain (Gly13Arg, fibrinogen Nanning) causes congenital dysfibrinogenemia associated with defective peptide A release.

Yan J, Luo M, Cheng P, Liao L, Deng X, Deng D, Lin F. Yan J, et al. Int J Hematol. 2017 Apr;105(4):506-514. doi: 10.1007/s12185-016-2157-1. Epub 2016 Dec 8. Int J Hematol. 2017. PMID: 27933517

7

Combined use of Clauss and prothrombin time-derived methods for determining fibrinogen concentrations: Screening for congenital dysfibrinogenemia.

Xiang L, Luo M, Yan J, Liao L, Zhou W, Deng X, Deng D, Cheng P, Lin F. Xiang L, et al. Among authors: yan j. J Clin Lab Anal. 2018 May;32(4):e22322. doi: 10.1002/jcla.22322. Epub 2017 Sep 18. J Clin Lab Anal. 2018. PMID: 28922493 Free PMC article.

8

Management of dysfibrinogenemia in pregnancy: A case report.

Yan J, Deng D, Cheng P, Liao L, Luo M, Lin F. Yan J, et al. J Clin Lab Anal. 2018 Mar;32(3):e22319. doi: 10.1002/jcla.22319. Epub 2017 Sep 26. J Clin Lab Anal. 2018. PMID: 28948631 Free PMC article.

9

[Surgical treatment of two patients with asymptomatic hereditary abnormal fibrinogen].

Luo ML, Yan J, Lin FQ, Cheng P, Deng DH. Luo ML, et al. Among authors: yan j. Zhonghua Xue Ye Xue Za Zhi. 2017 Sep 14;38(9):797-798. doi: 10.3760/cma.j.issn.0253-2727.2017.09.013. Zhonghua Xue Ye Xue Za Zhi. 2017. PMID: 29081199 Free PMC article. Chinese. No abstract available.

10

Rare LPL gene missense mutation in an infant with hypertriglyceridemia.

Qin YY, Wei AQ, Shan QW, Xian XY, Wu YY, Liao L, Yan J, Lai ZF, Lin FQ. Qin YY, et al. Among authors: yan j. J Clin Lab Anal. 2018 Jul;32(6):e22414. doi: 10.1002/jcla.22414. Epub 2018 Feb 25. J Clin Lab Anal. 2018. PMID: 29479812 Free PMC article.

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