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Flora Peyvandi

Showing results (231-240 of 610) with videos related to

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Pain and Therapy|January 12, 2022
Current and Emerging Approaches for Pain Management in Hemophilic ArthropathyRoberta Gualtierotti, Francesco Tafuri, Sara Arcudi, et al.
Thrombosis and Haemostasis|March 30, 2007
Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defectsLuca Monaldini, Rosanna Asselta, Stefano Duga, et al.
British Journal of Haematology|July 5, 2007
ADAMTS13 activity to antigen ratio in physiological and pathological conditions associated with an increased risk of thrombosisHendrik B Feys, Maria T Canciani, Flora Peyvandi, et al.
Internal and Emergency Medicine|October 14, 2022
Prescription appropriateness of anticoagulant drugs for prophylaxis of venous thromboembolism in hospitalized multimorbid older patientsRaffaella Rossio, Sara Mandelli, Ilaria Ardoino, et al.
Blood|January 1, 2010
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNARosanna Asselta, Valeria Rimoldi, Ilaria Guella, et al.
Research and Practice in Thrombosis and Haemostasis|July 1, 2024
Variant p.Tyr1584Cys: a frequent von Willebrand factor variant in search of von Willebrand diseaseOmid Seidizadeh, Luciano Baronciani, Paola Colpani, et al.
Biophysical Journal|May 27, 2008
Mechanistic studies on ADAMTS13 catalysisEnrico Di Stasio, Stefano Lancellotti, Flora Peyvandi, et al.
Internal and Emergency Medicine|February 14, 2024
Statins, ACE/ARBs drug use, and risk of pneumonia in hospitalized older patients: a retrospective cohort studyCarlotta Franchi, Raffaella Rossio, Sara Mandelli, et al.
Haematologica|August 6, 2002
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemiaRosanna Asselta, Silvia Spena, Stefano Duga, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 22, 2022
The dominant p.Thr274Pro mutation in the von Willebrand factor propeptide causes the von Willebrand disease type 1 phenotype in two unrelated patientsMaria Teresa Pagliari, Luciano Baronciani, Chiara Cordiglieri, et al.
Pageof 61

Showing results (231-240 of 610) with videos related to

Sort By:
Pageof 61
Pain and Therapy|January 12, 2022
Current and Emerging Approaches for Pain Management in Hemophilic ArthropathyRoberta Gualtierotti, Francesco Tafuri, Sara Arcudi, et al.
Thrombosis and Haemostasis|March 30, 2007
Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defectsLuca Monaldini, Rosanna Asselta, Stefano Duga, et al.
British Journal of Haematology|July 5, 2007
ADAMTS13 activity to antigen ratio in physiological and pathological conditions associated with an increased risk of thrombosisHendrik B Feys, Maria T Canciani, Flora Peyvandi, et al.
Internal and Emergency Medicine|October 14, 2022
Prescription appropriateness of anticoagulant drugs for prophylaxis of venous thromboembolism in hospitalized multimorbid older patientsRaffaella Rossio, Sara Mandelli, Ilaria Ardoino, et al.
Blood|January 1, 2010
Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNARosanna Asselta, Valeria Rimoldi, Ilaria Guella, et al.
Research and Practice in Thrombosis and Haemostasis|July 1, 2024
Variant p.Tyr1584Cys: a frequent von Willebrand factor variant in search of von Willebrand diseaseOmid Seidizadeh, Luciano Baronciani, Paola Colpani, et al.
Biophysical Journal|May 27, 2008
Mechanistic studies on ADAMTS13 catalysisEnrico Di Stasio, Stefano Lancellotti, Flora Peyvandi, et al.
Internal and Emergency Medicine|February 14, 2024
Statins, ACE/ARBs drug use, and risk of pneumonia in hospitalized older patients: a retrospective cohort studyCarlotta Franchi, Raffaella Rossio, Sara Mandelli, et al.
Haematologica|August 6, 2002
Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemiaRosanna Asselta, Silvia Spena, Stefano Duga, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|January 22, 2022
The dominant p.Thr274Pro mutation in the von Willebrand factor propeptide causes the von Willebrand disease type 1 phenotype in two unrelated patientsMaria Teresa Pagliari, Luciano Baronciani, Chiara Cordiglieri, et al.
Pageof 61