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Haemophilia : the Official Journal of the World Federation of Hemophilia|June 25, 2008
Rare bleeding disordersF Peyvandi, M Cattaneo, A Inbal, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|May 9, 2015
Long-term prophylaxis in severe factor VII deficiencyS M Siboni, E Biguzzi, C Mistretta, et al.Human Mutation|September 21, 2005
Role of the 2 adenine (g.11293_11294insAA) insertion polymorphism in the 3' untranslated region of the factor VII (FVII) gene: molecular characterization of a patient with severe FVII deficiencyF Peyvandi, I Garagiola, R Palla, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|April 26, 2014
Joint WFH-ISTH session: issues in clinical trial designF Peyvandi, A Farrugia, A Iorio, et al.International Journal of Laboratory Hematology|May 11, 2016
Report on the International Society for Laboratory Hematology Survey on guidelines to support clinical hematology laboratory practiceC P M Hayward, K A Moffat, T I George, et al.Journal of Thrombosis and Haemostasis : JTH|January 20, 2006
Platelet function analyzer (PFA)-100 closure time in the evaluation of platelet disorders and platelet functionC P M Hayward, P Harrison, M Cattaneo, et al.Thrombosis and Haemostasis|May 1, 1996
Factor V (Arg 506-->Gln) mutation in young survivors of myocardial infarctionD Ardissino, F Peyvandi, P A Merlini, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|July 6, 2007
Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in IndiaG Jayandharan, M Spreafico, A Viswabandya, et al.Journal of Thrombosis and Haemostasis : JTH|June 30, 2011
Fibrinogen replacement therapy for congenital fibrinogen deficiencyL Bornikova, F Peyvandi, G Allen, et al.American Journal of Hematology|September 25, 2004
Presentation and pattern of symptoms in 382 patients with Glanzmann thrombasthenia in IranG Toogeh, R Sharifian, M Lak, et al.Pageof 15