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Recurrent deep vein thrombosis and two coagulation factor gene mutations: quo vadis? (comment)

机译：复发性深静脉血栓形成和两个凝血因子基因突变：vadis？（评论）

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《Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis》 |1999年第6期|共3页
作者
Lensing AW; Prins MH;
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原文格式 PDF
正文语种 eng
中图分类心脏、血管（循环系）疾病;神经病学;
关键词
Factor V; Mutation; Prothrombin; Thrombophlebitis; 因子Ⅴ; 突变; 凝血酶原; 血栓性静脉炎;

机译：Factor V;Mutation;Prothrombin;Thrombophlebitis;因子Ⅴ;突变;凝血酶原;血栓性静脉炎;

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专利

1. Recurrent deep vein thrombosis and two coagulation factor gene mutations: quo vadis? (comment) [J] . Lensing AW, Prins MH Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis . 1999,第6期

机译：复发性深静脉血栓形成和两个凝血因子基因突变：vadis？（评论）
2. Prothrombin G20210A, factor V Leiden, and factor XIII Val34Leu: common mutations of blood coagulation factors and deep vein thrombosis in Austria. [J] . Renner W, Koppel H, Hoffmann C, Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis . 2000,第1期

机译：凝血酶原G20210A，因子V莱顿和因子XIII Val34Leu：奥地利的凝血因子和深静脉血栓形成的常见突变。
3. Congenital absence of the inferior vena cava and genetic coagulation abnormalities: a rare associated risk factor for recurrent idiopathic deep vein thrombosis. [J] . Parma M, Belotti D, Marinoni S, Clinical and applied thrombosis/hemostasis . 2003,第4期

机译：先天性下腔静脉缺失和遗传性凝血异常：罕见的复发性特发性深静脉血栓形成相关危险因素。
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. Biophysical Mechanisms Regulating Von Willebrand Disease, Arterial Thrombosis, and Deep Vein Thrombosis in Microfluidic Models of Vascular Injury [D] . Lehmann, Marcus. 2017

机译：血管损伤微流体模型中von Willebrand病，动脉血栓性疾病，动脉血栓形成和深静脉血栓形成的生物物理机制
6. Low prevalence of activated protein C resistance and coagulation factor V Arg506 to Gln mutation among Korean patients with deep vein thrombosis. [O] . T. W. Kim, W. K. Kim, J. H. Lee, 1998

机译：韩国深静脉血栓形成患者中活化蛋白C抗性和凝血因子V Arg506对Gln突变的患病率较低。
7. Congenital Absence of the Inferior Vena Cava and Genetic Coagulation Abnormalities: A Rare Associated Risk Factor for Recurrent Idiopathic Deep Vein Thrombosis [O] . Matteo Parma, Daniela Belotti, Sara Marinoni, 2003

机译：先天性缺失较差的腔静脉和遗传凝血异常：罕见的特发性深静脉血栓形成的罕见相关危险因素

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