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F Peyvandi

Showing results (41-50 of 166) with videos related to

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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.
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.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 5, 2011
The correlation between gene mutations and inhibitor development in patients with haemophilia A in southern IranS Haghpanah, M Sahraiian, A Afrasiabi, 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.
Journal of Thrombosis and Haemostasis : JTH|April 22, 2005
Factor VII gene polymorphisms are not associated with myocardial infarction in young womenF Peyvandi, L Bernardinelli, C H Martini, et al.
Thrombosis and Haemostasis|February 23, 2002
Short-term exposure to high altitude causes coagulation activation and inhibits fibrinolysisP M Mannucci, A Gringeri, F Peyvandi, et al.
Journal of Thrombosis and Haemostasis : JTH|August 13, 2003
Pattern of symptoms in 93 Iranian patients with severe factor XIII deficiencyM Lak, F Peyvandi, A Ali Sharifian, et al.
Journal of Thrombosis and Haemostasis : JTH|January 25, 2012
von Willebrand factor propeptide to antigen ratio in acquired thrombotic thrombocytopenic purpuraF Stufano, S LA Marca, S Pontiggia, et al.
Pageof 17

Showing results (41-50 of 166) with videos related to

Sort By:
Pageof 17
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.
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.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 5, 2011
The correlation between gene mutations and inhibitor development in patients with haemophilia A in southern IranS Haghpanah, M Sahraiian, A Afrasiabi, 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.
Journal of Thrombosis and Haemostasis : JTH|April 22, 2005
Factor VII gene polymorphisms are not associated with myocardial infarction in young womenF Peyvandi, L Bernardinelli, C H Martini, et al.
Thrombosis and Haemostasis|February 23, 2002
Short-term exposure to high altitude causes coagulation activation and inhibits fibrinolysisP M Mannucci, A Gringeri, F Peyvandi, et al.
Journal of Thrombosis and Haemostasis : JTH|August 13, 2003
Pattern of symptoms in 93 Iranian patients with severe factor XIII deficiencyM Lak, F Peyvandi, A Ali Sharifian, et al.
Journal of Thrombosis and Haemostasis : JTH|January 25, 2012
von Willebrand factor propeptide to antigen ratio in acquired thrombotic thrombocytopenic purpuraF Stufano, S LA Marca, S Pontiggia, et al.
Pageof 17