Li X - Search Results

1

Analysis of an Inherited Dysfibrinogenemia Pedigree Associated with a Heterozygous Mutation in the FGA Gene.

Li S, Wang M, Li X, Xu Q, Liu S, Luo S, Chen Y. Li S, et al. Among authors: li x. Hamostaseologie. 2020 Dec;40(5):642-648. doi: 10.1055/a-1261-3884. Epub 2020 Dec 29. Hamostaseologie. 2020. PMID: 33374030

2

[Analysis of a pedigree affected with congenital hypofibrinogenemia due to heterozygous Ser313Ile mutation of fibrinogen γ chain gene].

Zhu L, Zhao M, Cheng X, Yu D, Li X, Xu F, Wang J, Wang M. Zhu L, et al. Among authors: li x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10;35(2):179-183. doi: 10.3760/cma.j.issn.1003-9406.2018.02.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29652987 Chinese.

3

Genetic analysis of a pedigree with hereditary coagulation factor XI deficiency.

Zhou X, Zhang H, Wang M, Luo S, Liu S, Jin Y, Li X, Yang L. Zhou X, et al. Among authors: li x. Blood Coagul Fibrinolysis. 2019 Dec;30(8):413-418. doi: 10.1097/MBC.0000000000000857. Blood Coagul Fibrinolysis. 2019. PMID: 31567266

4

Phenotypic and Genotypic Analysis of a Hereditary Antithrombin Deficiency Pedigree Due to a Novel SERPINC1 Mutation (p.Met281Thr).

Liu S, Luo S, Yang L, Wang M, Jin Y, Li X, Xu Q. Liu S, et al. Among authors: li x. Hamostaseologie. 2020 Dec;40(5):687-690. doi: 10.1055/a-1145-4224. Epub 2020 May 25. Hamostaseologie. 2020. PMID: 32450575

5

[Analysis of a Chinese pedigree affected with hereditary factor VII deficiency caused by compound heterozygous variants of F7 gene].

Liu M, Jin Y, Yang L, Xie H, Li X, Liu S, Luo S, Wang M. Liu M, et al. Among authors: li x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Jun 10;37(6):633-636. doi: 10.3760/cma.j.issn.1003-9406.2020.06.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32472540 Chinese.

6

Analysis of phenotype and genotype of a family with hereditary coagulation factor V deficiency caused by the compound heterozygous mutations.

Luo S, Liu S, Xu M, Li X, Zhang H, Jin Y, Yang L, Wang M. Luo S, et al. Among authors: li x. Blood Coagul Fibrinolysis. 2020 Oct;31(7):485-489. doi: 10.1097/MBC.0000000000000946. Blood Coagul Fibrinolysis. 2020. PMID: 32833806

7

A novel heterozygous mutation (γIIe367Thr) causes congenital dysfibrinogenemia in a Chinese family.

Luo S, Xu Q, Xie Y, Li X, Jin Y, Yang L, Liu S, Wang M. Luo S, et al. Among authors: li x. Blood Coagul Fibrinolysis. 2020 Dec;31(8):569-574. doi: 10.1097/MBC.0000000000000948. Blood Coagul Fibrinolysis. 2020. PMID: 32833807

8

[Phenotypic and genotypic analysis of a pedigree affected with hereditary protein C deficiency due to heterozygous deletional mutation of PROC gene].

Liu S, Yu F, Luo S, Li X, Jin Y, Yang L, Zhou X, Zhang H, Wang M. Liu S, et al. Among authors: li x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Oct 10;37(10):1108-1112. doi: 10.3760/cma.j.cn511374-20190625-00312. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32924112 Chinese.

9

[Genetic analysis and clinical features of a pedigree affected with hereditary coagulation factor Ⅶ deficiency caused by compound heterozygotic mutations].

Jin Y, Yang L, Zhang F, Liu M, Su K, Li X, Wang M. Jin Y, et al. Among authors: li x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Oct 10;36(10):1006-1009. doi: 10.3760/cma.j.issn.1003-9406.2019.10.014. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31598947 Chinese.

10

A novel homozygous mutation (Gly1715Ser) causing hereditary factor V deficiency in a Chinese patient.

Liu S, Luo S, Yang L, Jin Y, Xie H, Xie Y, Li X, Wang M. Liu S, et al. Among authors: li x. Blood Coagul Fibrinolysis. 2020 Jan;31(1):71-76. doi: 10.1097/MBC.0000000000000871. Blood Coagul Fibrinolysis. 2020. PMID: 31789663

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