Marbet G A, Duckert F, Biland L, Widmer L K
Schweiz Med Wochenschr. 1985 Oct 26;115(43):1505-6.
Extensive haemostasis analysis in 373 patients with recurrent idiopathic venous thrombosis revealed insufficient fibrinolysis activation by the venous occlusion test in 48%. A case with antithrombin III dysfunction was the only inherited anomaly.
对373例复发性特发性静脉血栓形成患者进行的广泛止血分析显示,48%的患者通过静脉闭塞试验发现纤溶激活不足。1例抗凝血酶III功能障碍患者是唯一的遗传性异常病例。