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Thrombosis and Haemostasis|February 1, 1993
The genetic defect of type I von Willebrand disease "Vicenza" is linked to the von Willebrand factor geneA M Randi, E Sacchi, G C Castaman, et al.
European Journal of Internal Medicine|June 17, 2018
Implementation of the Frailty Index in hospitalized older patients: Results from the REPOSI registerM Cesari, C Franchi, L Cortesi, et al.
Journal of Thrombosis and Haemostasis : JTH|May 20, 2008
High thrombin generation measured in the presence of thrombomodulin is associated with an increased risk of recurrent venous thromboembolismA Tripodi, C Legnani, V Chantarangkul, et al.
Thrombosis Research|October 1, 1990
A prothrombin time-based functional assay of protein SL Preda, A Tripodi, C Valsecchi, et al.
Journal of Neurosurgical Sciences|January 1, 1983
Intracranial bleeding in haemophilia. A study of eleven casesA Federici, P M Mannucci, D Minetti, et al.
Human Genetics|May 1, 1988
Characterization of a partial deletion of the factor VIII gene in a haemophiliac with inhibitorB Bardoni, M Sampietro, M Romano, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 3, 2004
Comparison of attitudes towards prenatal diagnosis and termination of pregnancy for haemophilia in Iran and ItalyM Karimi, F Peyvandi, S Siboni, et al.
Thrombosis and Haemostasis|November 3, 1998
The post-thrombotic syndrome in young women: retrospective evaluation of prognostic factorsE Biguzzi, E Mozzi, A Alatri, et al.
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