Showing results (541-550 of 1,150) with videos related to
Sort By:
Pageof 115
Thrombosis and Haemostasis|November 3, 1998
High prevalence of hyperchomocysteinemia in patients with inflammatory bowel disease: a pathogenic link with thromboembolic complications?M Cattaneo, M Vecchi, M L Zighetti, et al.Blood|May 26, 1999
Low platelet alpha2beta1 levels in type I von Willebrand disease correlate with impaired platelet function in a high shear stress systemJ Di Paola, A B Federici, P M Mannucci, et al.Scandinavian Journal of Haematology|January 1, 1978
Sensitivity and precision of activated partial thromboplastin time (APTT) methods. A multicenter studyN Refsum, D Collen, H C Godal, et al.British Journal of Haematology|February 26, 2000
A novel polymorphism in intron 1a of the human factor VII gene (G73A): study of a healthy Italian population and of 190 young survivors of myocardial infarctionF Peyvandi, P M Mannucci, P Bucciarelli, et al.European Journal of Neurology|May 21, 2010
Effect of prothrombin 19911 A>G polymorphism on the risk of cerebral sinus-venous thrombosisI Martinelli, P Bucciarelli, V De Stefano, et al.Blood|November 11, 1999
Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (factor V Leiden)E M Faioni, F Franchi, P Bucciarelli, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|February 19, 2014
Integrated postural analysis in children with haemophiliaE Boccalandro, G Pasta, P M Mannucci, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|April 13, 2017
Kreuth IV: European consensus proposals for treatment of haemophilia with coagulation factor concentratesP L F Giangrande, F Peyvandi, B O'Mahony, et al.Journal of Thrombosis and Haemostasis : JTH|June 28, 2005
The first ambulatory screening on thromboembolism: a multicentre, cross-sectional, observational study on risk factors for venous thromboembolismG Di Minno, P M Mannucci, A Tufano, et al.Blood|September 26, 2000
Afibrinogenemia: first identification of a splicing mutation in the fibrinogen gamma chain gene leading to a major gamma chain truncationR Asselta, S Duga, T Simonic, et al.Pageof 115