Last Posted: Jul 23, 2019
- Risk of bleeding and thrombosis in inherited qualitative fibrinogen disorders.
Castaman Giancarlo, et al. European journal of haematology 2019 7
- Diagnosis of congenital fibrinogen disorders.
Lebreton Aurélien, et al. Annales de biologie clinique 2016 8 (4) 405-412
- Dysfibrinogenemia developed in a pregnant woman who has fibrinogen A?Thr312Ala (ACT/GCT) polymorphism.
Yamaguchi Ayaka, et al. [Rinsho? ketsueki] The Japanese journal of clinical hematology 2016 0 (1) 31-5
- Thromboelastography predicts risks of obstetric complication occurrence in (hypo)dysfibrinogenemia patients under non-pregnant state.
Zhou Jingyi, et al. Clinical and experimental pharmacology & physiology 2015 10
- [Congenital hypofibrinogenemia associated with a novel mutation in FGG gene].
Wang Yingyu, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2015 6 (3) 331-4
- Two symptomatic cases of dysfibrinogenemia in China: one with gamma-chain Arg275Cys mutation and another without detectable mutation in fibrinogen genes.
Bin Qiong, et al. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2015 7 (5) 564-71
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