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Flora Peyvandi

Showing results (321-330 of 610) with videos related to

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Pharmacogenomics|September 11, 2008
Effects of CYP2C9 and VKORC1 on INR variations and dose requirements during initial phase of anticoagulant therapyMarta Spreafico, Corrado Lodigiani, Y van Leeuwen, et al.
Pharmaceuticals (Basel, Switzerland)|October 27, 2022
Updates on Novel Non-Replacement Drugs for HemophiliaRoberta Gualtierotti, Samantha Pasca, Alessandro Ciavarella, et al.
Journal of Thrombosis and Haemostasis : JTH|July 5, 2025
The risk of cerebral vein thrombosis associated with different types of combined hormonal contraceptives: a case-control studyMaria Abbattista, Addolorata Truma, Ida Martinelli, et al.
Annals of Hematology|July 4, 2013
Global coagulation in myeloproliferative neoplasmsArmando Tripodi, Veena Chantarangkul, Francesca Gianniello, et al.
Thrombosis Research|April 3, 2014
Thrombin generation in patients with idiopathic sudden sensorineural hearing lossArmando Tripodi, Pasquale Capaccio, Lorenzo Pignataro, et al.
TH Open : Companion Journal to Thrombosis and Haemostasis|January 15, 2024
Surgical Experience from the STASEY Study of Emicizumab Prophylaxis in People with Hemophilia A with Factor VIII InhibitorsGiancarlo Castaman, Flora Peyvandi, Johanna A Kremer Hovinga, et al.
Haematologica|August 11, 2019
Profiling the mutational landscape of coagulation factor V deficiencyElvezia Maria Paraboschi, Marzia Menegatti, Valeria Rimoldi, et al.
Blood|June 21, 2003
Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V: Broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutationsMaria Claudia Montefusco, Stefano Duga, Rosanna Asselta, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 10, 2023
Diagnostic utility of bleeding assessment tools in congenital fibrinogen deficienciesSamin Mohsenian, Omid Seidizadeh, Roberta Palla, et al.
Journal of Lipid Research|August 12, 2010
Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian populationIlaria Guella, Rosanna Asselta, Diego Ardissino, et al.
Pageof 61

Showing results (321-330 of 610) with videos related to

Sort By:
Pageof 61
Pharmacogenomics|September 11, 2008
Effects of CYP2C9 and VKORC1 on INR variations and dose requirements during initial phase of anticoagulant therapyMarta Spreafico, Corrado Lodigiani, Y van Leeuwen, et al.
Pharmaceuticals (Basel, Switzerland)|October 27, 2022
Updates on Novel Non-Replacement Drugs for HemophiliaRoberta Gualtierotti, Samantha Pasca, Alessandro Ciavarella, et al.
Journal of Thrombosis and Haemostasis : JTH|July 5, 2025
The risk of cerebral vein thrombosis associated with different types of combined hormonal contraceptives: a case-control studyMaria Abbattista, Addolorata Truma, Ida Martinelli, et al.
Annals of Hematology|July 4, 2013
Global coagulation in myeloproliferative neoplasmsArmando Tripodi, Veena Chantarangkul, Francesca Gianniello, et al.
Thrombosis Research|April 3, 2014
Thrombin generation in patients with idiopathic sudden sensorineural hearing lossArmando Tripodi, Pasquale Capaccio, Lorenzo Pignataro, et al.
TH Open : Companion Journal to Thrombosis and Haemostasis|January 15, 2024
Surgical Experience from the STASEY Study of Emicizumab Prophylaxis in People with Hemophilia A with Factor VIII InhibitorsGiancarlo Castaman, Flora Peyvandi, Johanna A Kremer Hovinga, et al.
Haematologica|August 11, 2019
Profiling the mutational landscape of coagulation factor V deficiencyElvezia Maria Paraboschi, Marzia Menegatti, Valeria Rimoldi, et al.
Blood|June 21, 2003
Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V: Broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutationsMaria Claudia Montefusco, Stefano Duga, Rosanna Asselta, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 10, 2023
Diagnostic utility of bleeding assessment tools in congenital fibrinogen deficienciesSamin Mohsenian, Omid Seidizadeh, Roberta Palla, et al.
Journal of Lipid Research|August 12, 2010
Effects of PCSK9 genetic variants on plasma LDL cholesterol levels and risk of premature myocardial infarction in the Italian populationIlaria Guella, Rosanna Asselta, Diego Ardissino, et al.
Pageof 61