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Blood|December 12, 2001
Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen A alpha-chain gene are not associated with the decay of the mutant mRNAsR Asselta, S Duga, S Spena, et al.Journal of Thrombosis and Haemostasis : JTH|July 15, 2010
The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature diseaseP M Mannucci, R Asselta, S Duga, et al.The British Journal of Surgery|June 12, 2013
Raised haematocrit concentration and the risk of death and vascular complications after major surgeryK M Musallam, J B Porter, P M Sfeir, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|August 23, 2011
Efficacy of prophylaxis and genotype-phenotype correlation in patients with severe Factor X deficiency in IranM Karimi, A Vafafar, S Haghpanah, et al.Journal of Thrombosis and Haemostasis : JTH|April 30, 2013
A synonymous (c.3390C>T) or a splice-site (c.3380-2A>G) mutation causes exon 26 skipping in four patients with von Willebrand disease (2A/IIE)M T Pagliari, L Baronciani, I Garcìa Oya, et al.Journal of Thrombosis and Haemostasis : JTH|April 27, 2017
Caplacizumab reduces the frequency of major thromboembolic events, exacerbations and death in patients with acquired thrombotic thrombocytopenic purpuraF Peyvandi, M Scully, J A Kremer Hovinga, et al.Journal of Thrombosis and Haemostasis : JTH|July 6, 2011
Platelet reactive conformation and multimeric pattern of von Willebrand factor in acquired thrombotic thrombocytopenic purpura during acute disease and remissionL A Lotta, R Lombardi, M Mariani, et al.Journal of Thrombosis and Haemostasis : JTH|October 13, 2018
Hemostatic abnormalities in patients with Ehlers-Danlos syndromeA Artoni, A Bassotti, M Abbattista, et al.Journal of Thrombosis and Haemostasis : JTH|May 25, 2011
Oxidized von Willebrand factor is efficiently cleaved by serine proteases from primary granules of leukocytes: divergence from ADAMTS-13S Lancellotti, V De Filippis, N Pozzi, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|May 5, 2011
Central nervous system bleeding in patients with rare bleeding disordersS M Siboni, E Zanon, G Sottilotta, et al.Pageof 15