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F Peyvandi

Showing results (71-80 of 166) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|August 7, 2016
Recommendations for authors of manuscripts reporting inhibitor cases developed in previously treated patients with hemophilia: communication from the SSC of the ISTHA Iorio, A M Barbara, F Bernardi, et al.
Thrombosis and Haemostasis|April 1, 1996
Frequency of factor V Arg506 Gln in ItaliansP M Mannucci, F Duca, F Peyvandi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 28, 2017
Molecular investigation of 41 patients affected by coagulation factor XI deficiencyV Rimoldi, E M Paraboschi, M Menegatti, et al.
Journal of Thrombosis and Haemostasis : JTH|May 26, 2010
No association between chromosome 12p13 single nucleotide polymorphisms and early-onset ischemic strokeL A Lotta, B Giusti, C Saracini, et al.
Journal of Thrombosis and Haemostasis : JTH|August 24, 2010
Factor XIII--an under diagnosed deficiency--are we using the right assays?A S Lawrie, L Green, I J Mackie, et al.
British Journal of Haematology|August 8, 1998
Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patientsF Peyvandi, P M Mannucci, M Lak, et al.
Clinical and Laboratory Haematology|September 24, 2005
Glanzmann thrombasthenia and Bernard-Soulier syndrome in south IranA Afrasiabi, A Afrabiasi, A Artoni, et al.
Journal of Thrombosis and Haemostasis : JTH|January 22, 2010
ADAMTS-13 assays in thrombotic thrombocytopenic purpuraF Peyvandi, R Palla, L A Lotta, et al.
Journal of Thrombosis and Haemostasis : JTH|April 24, 2012
Elevated prepartum fibrinogen levels are not associated with a reduced risk of postpartum hemorrhageF Peyvandi, E Biguzzi, F Franchi, et al.
Thrombosis and Haemostasis|November 1, 2000
Homozygous 2bp deletion in the human factor VII gene: a non-lethal mutation that is associated with a complete absence of circulating factor VIIF Peyvandi, P M Mannucci, P V Jenkins, et al.
Pageof 17

Showing results (71-80 of 166) with videos related to

Sort By:
Pageof 17
Journal of Thrombosis and Haemostasis : JTH|August 7, 2016
Recommendations for authors of manuscripts reporting inhibitor cases developed in previously treated patients with hemophilia: communication from the SSC of the ISTHA Iorio, A M Barbara, F Bernardi, et al.
Thrombosis and Haemostasis|April 1, 1996
Frequency of factor V Arg506 Gln in ItaliansP M Mannucci, F Duca, F Peyvandi, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 28, 2017
Molecular investigation of 41 patients affected by coagulation factor XI deficiencyV Rimoldi, E M Paraboschi, M Menegatti, et al.
Journal of Thrombosis and Haemostasis : JTH|May 26, 2010
No association between chromosome 12p13 single nucleotide polymorphisms and early-onset ischemic strokeL A Lotta, B Giusti, C Saracini, et al.
Journal of Thrombosis and Haemostasis : JTH|August 24, 2010
Factor XIII--an under diagnosed deficiency--are we using the right assays?A S Lawrie, L Green, I J Mackie, et al.
British Journal of Haematology|August 8, 1998
Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patientsF Peyvandi, P M Mannucci, M Lak, et al.
Clinical and Laboratory Haematology|September 24, 2005
Glanzmann thrombasthenia and Bernard-Soulier syndrome in south IranA Afrasiabi, A Afrabiasi, A Artoni, et al.
Journal of Thrombosis and Haemostasis : JTH|January 22, 2010
ADAMTS-13 assays in thrombotic thrombocytopenic purpuraF Peyvandi, R Palla, L A Lotta, et al.
Journal of Thrombosis and Haemostasis : JTH|April 24, 2012
Elevated prepartum fibrinogen levels are not associated with a reduced risk of postpartum hemorrhageF Peyvandi, E Biguzzi, F Franchi, et al.
Thrombosis and Haemostasis|November 1, 2000
Homozygous 2bp deletion in the human factor VII gene: a non-lethal mutation that is associated with a complete absence of circulating factor VIIF Peyvandi, P M Mannucci, P V Jenkins, et al.
Pageof 17