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Thrombosis and Haemostasis|December 2, 1991
Antithrombin III: a database of mutationsD A Lane, H Ireland, R J Olds, 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.FEBS Letters|June 18, 1990
Antithrombin Rouen-IV 24 Arg----Cys. The amino-terminal contribution to heparin bindingJ Y Borg, S O Brennan, R W Carrell, 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.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|April 1, 1997
Asymptomatic coinheritance of heterozygous plasminogen deficiency and the factor VLeiden mutationM D McColl, R C Tait, I D Walker, et al.FEBS Letters|October 29, 1990
Antithrombin Dublin (-3 Val----Glu): an N-terminal variant which has an aberrant signal peptidase cleavage siteM Daly, D Bruce, D J Perry, 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.Journal of Thrombosis and Haemostasis : JTH|November 29, 2015
Thrombotic microangiopathy without renal involvement: two novel mutations in complement-regulator genesF Peyvandi, R Rossio, B Ferrari, et al.Pageof 24