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Factor V Leiden mutation, prothrombin gene mutation, and deficiencies in coagulation inhibitors associated with Budd-Chiari syndrome and portal vein thrombosis: results of a case-control study

机译：因子V莱顿突变，凝血酶原基因突变以及与Budd-Chiari综合征和门静脉血栓形成相关的凝血抑制剂缺乏：病例对照研究的结果

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Janssen H.L.A. (Harry); Vandenbroucke J.P.; Rosendaal F.R. (Frits); Hoek B. (Bart) van; Meinardi J.R.; Vleggaar F.P. (Frank); Uum S.H. van; Haagsma E.B. (Els); Meer F.J.M. van der; Hattum J. (Jan) van; Chamuleau R.A.; Adang R.P.R. (Rob);
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1. Associations of Coagulation Factor V Leiden and Prothrombin G20210A Mutations With Budd-Chiari Syndrome and Portal Vein Thrombosis: A Systematic Review and Meta-analysis [J] . Qi Xingshun, Ren Weirong, De Stefano Valerio, Clinical gastroenterology and hepatology: the official clinical practice journal of the American Gastroenterological Association . 2014,第11期

机译：凝血因子V Leiden和凝血酶原G20210A突变与Budd-Chiari综合征和门静脉血栓形成的关联：系统评价和荟萃分析
2. Associations of Coagulation Factor V Leiden and Prothrombin G20210A Mutations With Budd-Chiari Syndrome and Portal Vein Thrombosis: A Systematic Review and Meta-analysis [J] . Qi Xingshun, Ren Weirong, De Stefano Valerio, Clinical gastroenterology and hepatology: the official clinical practice journal of the American Gastroenterological Association . 2014,第11期

机译：凝血因子V Leiden和凝血酶原G20210A突变与Budd-Chiari综合征和门静脉血栓形成的关联：系统评价和荟萃分析
3. Thrombophilic Genetic Factors PAI-1, MTHFRC677T, V Leiden 506Q, and Prothrombin 20210A in Noncirrhotic Portal Vein Thrombosis and Budd-Chiari Syndrome in a Caucasian Population [J] . MarioD’Amico, PietroSammarco, LindaPasta International Journal of Vascular Medicine . 2013,第287期

机译：高加索人群非肝硬化门静脉血栓形成和Budd-Chiari综合征的亲血性遗传因素PAI-1，MTHFRC677T，V Leiden 506Q和凝血酶原20210A
4. Deep Venoys Thrombosis of the Lower Extremity In a 16-Year-OIcl Girl with Homozygous MTHFR- and Heterozygous Factor? Leiden-Mutation [C] . B. Roschitz, W. Muntean, C. Mannhalter, Hemophilie-Symposion . 2004

机译：一个16岁女孩纯合的MTHFR和杂合因子的16岁女孩下肢深静脉血栓形成？莱顿突变
5. Risk factors for clinical manifestation in carriers of Factor V Leiden and prothrombin gene mutations. [D] . De Sancho, Maria. 2009

机译：因子V Leiden和凝血酶原基因突变携带者临床表现的危险因素。
6. Thrombophilic Genetic Factors PAI-1 MTHFRC677T V Leiden 506Q and Prothrombin 20210A in Noncirrhotic Portal Vein Thrombosis and Budd-Chiari Syndrome in a Caucasian Population [O] . Mario DAmico, Pietro Sammarco, Linda Pasta 2013

机译：高加索人群非肝硬化门静脉血栓形成和Budd-Chiari综合征中的血栓形成遗传因素PAI-1MTHFRC677TV Leiden 506Q和凝血酶原20210A
7. Prevalence of factor V Leiden mutation and other hereditary thrombophilic factors in Egyptian children with portal vein thrombosis: results of a single-center case-control study [O] . Hanaa El-Karaksy, Nehal El-Koofy, Manal El-Hawary, 2004

机译：埃及脉络血栓形成埃及儿童因子V林肯突变与其他遗传性血栓因子的患病率：单中心案例对照研究的结果

Factor V Leiden mutation, prothrombin gene mutation, and deficiencies in coagulation inhibitors associated with Budd-Chiari syndrome and portal vein thrombosis: results of a case-control study

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