Jin Y - Search Results

1

[A Meta-analysis of high-dose epinephrine in children with cardiopulmonary arrest].

Gu J, Jin Y, Yang KH, Liu YL, Tian JH, Ma B, Tan JY. Gu J, et al. Among authors: jin y. Zhonghua Er Ke Za Zhi. 2007 Sep;45(9):650-4. Zhonghua Er Ke Za Zhi. 2007. PMID: 18021553 Chinese.

2

The association between urinary tract infection during pregnancy and preeclampsia: A meta-analysis.

Yan L, Jin Y, Hang H, Yan B. Yan L, et al. Among authors: jin y. Medicine (Baltimore). 2018 Sep;97(36):e12192. doi: 10.1097/MD.0000000000012192. Medicine (Baltimore). 2018. PMID: 30200124 Free PMC article. Review.

3

[Association between the C46T polymorphism of coagulation factor Ⅻ gene and the involvement of factor Ⅻ activity in patients with unexplained recurrent spontaneous abortion].

Jin YH, Shen XL, Wang MS, Xu XM, Liu MN, Zhao ZS, Zheng JY. Jin YH, et al. Zhonghua Fu Chan Ke Za Zhi. 2016 Aug 25;51(8):597-601. doi: 10.3760/cma.j.issn.0529-567X.2016.08.009. Zhonghua Fu Chan Ke Za Zhi. 2016. PMID: 27561939 Chinese.

4

[Analysis of the molecular pathogenesis and clinical phenotypes of 10 patients with inherited coagulation factor Ⅺ deficiency].

Li SX, Jin YH, Yang LL, Xu QY, Li XL, Wang MS. Li SX, et al. Among authors: jin yh. Zhonghua Xue Ye Xue Za Zhi. 2020 Dec 14;41(12):1041-1043. doi: 10.3760/cma.j.issn.0253-2727.2020.12.013. Zhonghua Xue Ye Xue Za Zhi. 2020. PMID: 33445854 Free PMC article. Chinese. No abstract available.

5

[A family with hereditary FⅪ deficiency caused by compound heterozygous mutation].

Zheng XY, Jin YH, Xu YY, Yang LL, Zhu LQ, Wang HH, Jiang ST, Wang MS. Zheng XY, et al. Among authors: jin yh. Zhonghua Xue Ye Xue Za Zhi. 2021 Aug 14;42(8):687-689. doi: 10.3760/cma.j.issn.0253-2727.2021.08.014. Zhonghua Xue Ye Xue Za Zhi. 2021. PMID: 34547878 Free PMC article. Chinese. No abstract available.

6

[Phenotypic and genetic analysis of a pedigree with inherited antithrombin deficiency].

Xu QY, Jin YH, Zheng XY, Yang LL, Li XL, Zhang HY, Wang MS. Xu QY, et al. Among authors: jin yh. Zhonghua Xue Ye Xue Za Zhi. 2020 Jul 14;41(7):589-592. doi: 10.3760/cma.j.issn.0253-2727.2020.07.010. Zhonghua Xue Ye Xue Za Zhi. 2020. PMID: 32810967 Free PMC article. Chinese. No abstract available.

7

[Clinical phenotype and gene mutation analysis of 12 patients with hereditary protein C deficiency in different families].

Xu QY, Yang LL, Xie HX, Jin YH, Li XL, Zhou XX, Liu MN, Wang MS. Xu QY, et al. Among authors: jin yh. Zhonghua Xue Ye Xue Za Zhi. 2022 Jan 14;43(1):35-40. doi: 10.3760/cma.j.issn.0253-2727.2022.01.008. Zhonghua Xue Ye Xue Za Zhi. 2022. PMID: 35231991 Free PMC article. Chinese.

8

[A homozygous variant in a consanguineous pedigree with inherited protein S deficiency].

Xie HX, Jin YH, Yang LL, Xie YY, Liu SQ, Luo SS, Wang MS. Xie HX, et al. Among authors: jin yh. Zhonghua Jie He He Hu Xi Za Zhi. 2021 Apr 12;44(4):360-364. doi: 10.3760/cma.j.cn112147-20200511-00584. Zhonghua Jie He He Hu Xi Za Zhi. 2021. PMID: 33832024 Chinese.

9

[Analysis of a pedigree with inherited factor V deficiency caused by compound heterozygous mutation].

Guo YL, Kong WZ, Wan Q, Zheng WJY, Xi JQ, Liu SQ, Wang MS, Jin YH. Guo YL, et al. Among authors: jin yh. Zhonghua Xue Ye Xue Za Zhi. 2021 Feb 14;42(2):135-139. doi: 10.3760/cma.j.issn.0253-2727.2021.02.008. Zhonghua Xue Ye Xue Za Zhi. 2021. PMID: 33858044 Free PMC article. Chinese.

10

Reversible left ventricular dyssynchrony and dysfunction resulting from right ventricular pre-excitation.

Shan Q, Jin Y, Cao K. Shan Q, et al. Among authors: jin y. Europace. 2007 Aug;9(8):697-701. doi: 10.1093/europace/eum138. Epub 2007 Jul 14. Europace. 2007. PMID: 17630390

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