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A prospective cohort study on the absolute risks of venous thromboembolism and predictive value of screening asymptomatic relatives of patients with hereditary deficiencies of protein S, protein C or antithrombin

机译：一项前瞻性队列研究，探讨了遗传性蛋白质S，蛋白质C或抗凝血酶缺乏症患者静脉血栓栓塞的绝对风险和筛查无症状亲属的预测价值

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Mahmoodi, B. K.; Brouwer, J-L P.; Ten Kate, M. K.; Lijfering, W. M.; Veeger, N. J. G. M.; Mulder, A. B.; Kluin-Nelemans, H. C.; van der Meer, J.;
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年度 2010
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正文语种 eng
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1. A prospective cohort study on the absolute risks of venous thromboembolism and predictive value of screening asymptomatic relatives of patients with hereditary deficiencies of protein S, protein C or antithrombin [J] . MahmoodiB.K., BrouwerJ.-L.P., TenKateM.K., Journal of thrombosis and haemostasis: JTH . 2010,第6期

机译：前瞻性队列研究：遗传性蛋白质S，C或抗凝血酶缺乏症患者静脉血栓栓塞的绝对风险和筛查无症状亲属的预测价值
2. High long-term absolute risk of recurrent venous thromboembolism in patients with hereditary deficiencies of protein S, protein C or antithrombin. [J] . Brouwer JL, Lijfering WM, Ten-Kate MK, Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis . 2009,第1期

机译：患有遗传性S蛋白，C蛋白或抗凝血酶缺乏症的患者，长期复发性静脉血栓栓塞的绝对风险较高。
3. beta-Antithrombin, subtype of antithrombin deficiency and the risk of venous thromboembolism in hereditary antithrombin deficiency: A family cohort study [J] . Croles Frederik Nanne, Mulder Rene, Mulder Andre B., Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis . 2018,第期

机译：β-抗凝血酶，抗凝血酶缺乏的亚型和遗传性抗血栓缺乏症的静脉血栓栓塞风险：家庭队列研究
4. Resistin Protein Analysis Using Receiver Operating Characteristics Curve in Predicting the Occurrence of Type 2 Diabetes Mellitus in Respondents of Cohort Study of Risk Factors for Noncommunicable Diseases in Bogor [C] . Uly Alfi Nikmah, Asri Werdhasari, Frans Dany, International Symposium on Health Research;National Congress of The Indonesian Public Health Association . 2020

机译：使用接收器操作特性曲线预测茂物危险疾病危险因素群体患者患者2型糖尿病患者的抗性蛋白质分析
5. High prevalence of protein C protein S antithrombin deficiency and Factor V Leiden mutation as a cause of hereditary thrombophilia in patients of venous thromboembolism and cerebrovascular accident [O] . Nadir Ali, Muhammad Ayyub, Saleem Ahmed Khan 2014

机译：静脉血栓栓塞和脑血管意外患者中蛋白C蛋白S抗凝血酶缺乏症和因子V莱顿突变的高患病率是遗传性血栓形成的原因
6. A prospective cohort study on the absolute risks of venous thromboembolism and predictive value of screening asymptomatic relatives of patients with hereditary deficiencies of protein S, protein C or antithrombin [O] . Mahmoodi, B. K., Brouwer, J-L P., Ten Kate, M. K., 2010

机译：一项前瞻性队列研究，探讨了遗传性蛋白质S，蛋白质C或抗凝血酶缺乏症患者静脉血栓栓塞的绝对风险和筛查无症状亲属的预测价值

A prospective cohort study on the absolute risks of venous thromboembolism and predictive value of screening asymptomatic relatives of patients with hereditary deficiencies of protein S, protein C or antithrombin

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