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British Journal of Haematology|June 1, 1993
Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381-->Ser) in the substrate-binding pocketG Marchetti, P Patracchini, D Gemmati, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|January 5, 2008
Management of menorrhagia in women with inherited bleeding disorders: general principles and use of desmopressinF RodeghieroHaemophilia : the Official Journal of the World Federation of Hemophilia|May 16, 2002
von Willebrand disease: still an intriguing disorder in the era of molecular medicineF RodeghieroClinical Chemistry|May 1, 1991
Fibrinogen assays: a collaborative study of six different methods. C.I.S.M.E.L. Comitato Italiano per la Standardizzazione dei Metodi in Ematologia e LaboratorioG Palareti, M Maccaferri, C Manotti, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|January 5, 2008
Desmopressin for the treatment of haemophiliaG CastamanThrombosis and Haemostasis|September 1, 1994
Clinical manifestations and management of inherited thrombophilia: retrospective analysis and follow-up after diagnosis of 238 patients with congenital deficiency of antithrombin III, protein C, protein SV De Stefano, G Leone, S Mastrangelo, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|November 22, 2007
Molecular characterization of five Italian families with inherited severe factor XIII deficiencyG Castaman, S H Giacomelli, V Ivaskevicius, et al.Journal of Thrombosis and Haemostasis : JTH|June 22, 2011
Deep intronic variations may cause mild hemophilia AG Castaman, S H Giacomelli, M E Mancuso, et al.Thrombosis and Haemostasis|February 11, 2000
Von Willebrand Disease type 2M "Vicenza" in Italian and German patients: identification of the first candidate mutation (G3864A; R1205H) in 8 familiesR Schneppenheim, A B Federici, U Budde, et al.Pageof 81