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Haemophilia : the Official Journal of the World Federation of Hemophilia|October 28, 2016
von Willebrand disease type 1 mutation p.Arg1379Cys and the variant p.Ala1377Val synergistically determine a 2M phenotype in four Italian patientsM T Pagliari, L Baronciani, F Stufano, et al.Journal of Thrombosis and Haemostasis : JTH|January 30, 2009
Platelet adhesion to multimerin 1 in vitro: influences of platelet membrane receptors, von Willebrand factor and shearS Tasneem, F Adam, I Minullina, et al.International Journal of Laboratory Hematology|April 23, 2014
Evaluation of an automated method for measuring von Willebrand factor activity in clinical samples without ristocetinL Graf, K A Moffat, S A Carlino, et al.Journal of Thrombosis and Haemostasis : JTH|April 21, 2016
Reduced fibrinolytic resistance in patients with factor XI deficiency. Evidence of a thrombin-independent impairment of the thrombin-activatable fibrinolysis inhibitor pathwayM Colucci, F Incampo, A Cannavò, et al.Journal of Thrombosis and Haemostasis : JTH|July 23, 2003
Severe factor V deficiency: exon skipping in the factor V gene causing a partial deletion of the C1 domainR Asselta, M C Montefusco, S Duga, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|September 3, 2013
Orthopaedic surgery in patients with von Willebrand diseaseS M Siboni, E Biguzzi, L P Solimeno, et al.Thrombosis and Haemostasis|November 1, 2000
Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand diseaseL Baronciani, G Cozzi, M T Canciani, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|October 22, 2014
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 womenE Biguzzi, F Franchi, B Acaia, et al.Thrombosis and Haemostasis|August 26, 2000
Molecular characterisation and three-dimensional structural analysis of mutations in 21 unrelated families with inherited factor VII deficiencyF Peyvandi, P V Jenkins, P M Mannucci, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|July 23, 2011
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiencyE M Paraboschi, S M Kayiran, N Özbek, et al.Pageof 15