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Clinica Chimica Acta; International Journal of Clinical Chemistry|January 22, 2022
Congenital dysfibrinogenemia in major surgery: A description of four cases and review of the literatureJie Yan, Meiling Luo, Liqun Xiang, et al.
Laboratory Medicine|November 14, 2025
Congenital hypofibrinogenemia with bleeding risk: mutations in the FGA, FGB, and FGG genesYangyang Wu, Kaili Qin, Liqun Xiang, et al.
Plos One|November 1, 2023
Association between total bilirubin/Albumin ratio and all-cause mortality in acute kidney injury patients: A retrospective cohort studyXimei Huang, Yunhua Huang, Min Chen, et al.
Medicine|September 27, 2024
Evaluation of alarm notification of artificial intelligence in automated analyzer detection of parasitesZila Wang, Lin Liao, Ximei Huang, et al.
Hematology (Amsterdam, Netherlands)|March 5, 2021
Congenital dysfibrinogenemia caused by γAla327Val mutation: structural abnormality of D regionAiqiu Wei, Yangyang Wu, Liqun Xiang, et al.
Journal of Clinical Laboratory Analysis|September 27, 2017
Management of dysfibrinogenemia in pregnancy: A case reportJie Yan, Donghong Deng, Peng Cheng, et al.
Genetic Testing and Molecular Biomarkers|March 29, 2022
Clinical Significance and Prognostic Value of Lactate Dehydrogenase Expression in Cervical CancerYuping Ye, Min Chen, Xinyan Chen, et al.
Cell Proliferation|October 15, 2025
Pulmonary Vascular Endothelial Cells in Lung Diseases: Mechanisms, Therapeutic Strategies, and Future DirectionsQianyue Liu, Hongshuai Zheng, Jing Liu, et al.
International Journal of Hematology|December 10, 2016
A novel mutation in the fibrinogen Aα chain (Gly13Arg, fibrinogen Nanning) causes congenital dysfibrinogenemia associated with defective peptide A releaseJie Yan, Meiling Luo, Peng Cheng, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 10, 2016
[Analysis of a family with congenital dysfibrinogenemia caused by an Arg275His mutation in the gamma chain of fibrinogen]Jie Yan, Donghong Deng, Xuelian Deng, et al.
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