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F Peyvandi

Showing results (31-40 of 166) with videos related to

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Orphanet Journal of Rare Diseases|July 15, 2020
Evolution of Haemophilia Care in Europe: 10 years of the principles of careD Noone, B O'Mahony, F Peyvandi, et al.
Journal of Thrombosis and Haemostasis : JTH|May 1, 2017
Pregnancy outcome after a first episode of cerebral vein thrombosis: replyI Martinelli, M Abbattista, E Somigliana, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 21, 2016
Efficacy, safety and pharmacokinetics of a new high-purity factor X concentrate in subjects with hereditary factor X deficiencyS K Austin, K Kavakli, M Norton, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 13, 2010
Evaluation of an automated platelet-based assay of ristocetin cofactor activityA S Lawrie, I J Mackie, S J Machin, et al.
British Journal of Haematology|October 16, 1999
Bleeding and thrombosis in 55 patients with inherited afibrinogenaemiaM Lak, M Keihani, F Elahi, et al.
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.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 27, 2007
A novel mutation of alpha2-plasmin inhibitor gene causes an inherited deficiency and a bleeding tendencyA Maino, I Garagiola, A Artoni, et al.
Journal of Thrombosis and Haemostasis : JTH|April 18, 2012
Measurement of anti-ADAMTS13 neutralizing autoantibodies: a comparison between CBA and FRET assaysI Mancini, C Valsecchi, R Palla, et al.
Journal of Thrombosis and Haemostasis : JTH|October 3, 2003
Warfarin and acenocoumarol dose requirements according to CYP2C9 genotyping in North-Italian patientsM Spreafico, F Peyvandi, D Pizzotti, et al.
Pageof 17

Showing results (31-40 of 166) with videos related to

Sort By:
Pageof 17
Orphanet Journal of Rare Diseases|July 15, 2020
Evolution of Haemophilia Care in Europe: 10 years of the principles of careD Noone, B O'Mahony, F Peyvandi, et al.
Journal of Thrombosis and Haemostasis : JTH|May 1, 2017
Pregnancy outcome after a first episode of cerebral vein thrombosis: replyI Martinelli, M Abbattista, E Somigliana, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 21, 2016
Efficacy, safety and pharmacokinetics of a new high-purity factor X concentrate in subjects with hereditary factor X deficiencyS K Austin, K Kavakli, M Norton, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 13, 2010
Evaluation of an automated platelet-based assay of ristocetin cofactor activityA S Lawrie, I J Mackie, S J Machin, et al.
British Journal of Haematology|October 16, 1999
Bleeding and thrombosis in 55 patients with inherited afibrinogenaemiaM Lak, M Keihani, F Elahi, et al.
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.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 27, 2007
A novel mutation of alpha2-plasmin inhibitor gene causes an inherited deficiency and a bleeding tendencyA Maino, I Garagiola, A Artoni, et al.
Journal of Thrombosis and Haemostasis : JTH|April 18, 2012
Measurement of anti-ADAMTS13 neutralizing autoantibodies: a comparison between CBA and FRET assaysI Mancini, C Valsecchi, R Palla, et al.
Journal of Thrombosis and Haemostasis : JTH|October 3, 2003
Warfarin and acenocoumarol dose requirements according to CYP2C9 genotyping in North-Italian patientsM Spreafico, F Peyvandi, D Pizzotti, et al.
Pageof 17