Jin YH - Search Results

1

[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.

2

[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.

3

[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.

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 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.

6

[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.

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

Comparison of Idiopathic Macular Hole Interventions Using Frequency Domain Optical Coherence Tomography and Optical Coherence Tomography Angiography.

Liu M, Jin Y, Li L, Yuan F, Xu Y. Liu M, et al. Dis Markers. 2022 Aug 13;2022:7749605. doi: 10.1155/2022/7749605. eCollection 2022. Dis Markers. 2022. PMID: 35996716 Free PMC article.

9

Diagnostic strategy of metagenomic next-generation sequencing for gram negative bacteria in respiratory infections.

Liang W, Zhang Q, Qian Q, Wang M, Ding Y, Zhou J, Zhu Y, Jin Y, Chen X, Kong H, Song W, Lu X, Wu X, Xu X, Dai S, Sun W. Liang W, et al. Ann Clin Microbiol Antimicrob. 2024 Feb 1;23(1):10. doi: 10.1186/s12941-024-00670-x. Ann Clin Microbiol Antimicrob. 2024. PMID: 38302964 Free PMC article.

10

[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. Zhonghua Er Ke Za Zhi. 2007 Sep;45(9):650-4. Zhonghua Er Ke Za Zhi. 2007. PMID: 18021553 Chinese.

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