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British Journal of Haematology|September 21, 2000
Second malignancies in patients with essential thrombocythaemia treated with busulphan and hydroxyurea: long-term follow-up of a randomized clinical trialG Finazzi, M Ruggeri, F Rodeghiero, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|April 2, 2009
Severe spontaneous arterial thrombotic manifestations in patients with inherited hypo- and afibrinogenemiaG Castaman, M Lunardi, L Rigo, et al.British Journal of Haematology|March 1, 1995
A novel candidate mutation (Arg611-->His) in type I 'platelet discordant' von Willebrand's disease with desmopressin-induced thrombocytopeniaG Castaman, J C Eikenboom, F Rodeghiero, et al.American Journal of Hematology|December 1, 1993
Multimeric pattern of plasma and platelet von Willebrand factor is normal in uremic patientsG Castaman, F Rodeghiero, A Lattuada, et al.British Journal of Haematology|January 29, 2000
Heightened proteolysis of the von Willebrand factor subunit in patients with von Willebrand disease hemizygous or homozygous for the C2362F mutationG Castaman, J C Eikenboom, A Lattuada, et al.Acta Haematologica|January 1, 1987
Recurrent life-threatening epistaxis in a child with Bernard-Soulier syndrome controlled by bilateral ligation of external carotids and ethmoidal arteriesF Rodeghiero, G Castaman, G Pesavento, et al.Blood|May 16, 1998
Molecular mechanisms of type II factor XIII deficiency: novel Gly562-Arg mutation and C-terminal truncation of the A subunit cause factor XIII deficiency as characterized in a mammalian expression systemN Takahashi, H Tsukamoto, H Umeyama, et al.Thrombosis and Haemostasis|May 6, 1998
Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian originJ C Eikenboom, G Castaman, H L Vos, et al.Haematologica|January 4, 1998
Pilot study on the safety and efficacy of desmopressin for the treatment or prevention of bleeding in patients with hematologic malignanciesG Castaman, E D Bona, C Schiavotto, et al.Journal of Thrombosis and Haemostasis : JTH|January 20, 2006
Factor VIII and von Willebrand factor changes after desmopressin and during pregnancy in type 2M von Willebrand disease Vicenza: a prospective study comparing patients with single (R1205H) and double (R1205H-M740I) defectG Castaman, A B Federici, M Bernardi, et al.Pageof 81