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Pain and Therapy
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January 12, 2022
Current and Emerging Approaches for Pain Management in Hemophilic Arthropathy
Roberta 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 defects
Luca 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 thrombosis
Hendrik 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 patients
Raffaella 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-mRNA
Rosanna 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 disease
Omid Seidizadeh, Luciano Baronciani, Paola Colpani, et al.
Biophysical Journal
|
May 27, 2008
Mechanistic studies on ADAMTS13 catalysis
Enrico 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 study
Carlotta 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 afibrinogenemia
Rosanna 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 patients
Maria Teresa Pagliari, Luciano Baronciani, Chiara Cordiglieri, et al.
Page
of 61
Search research articles
Search
Showing results (231-240 of 610) with videos related to
Sort By:
Page
of 61
Pain and Therapy
|
January 12, 2022
Current and Emerging Approaches for Pain Management in Hemophilic Arthropathy
Roberta 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 defects
Luca 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 thrombosis
Hendrik 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 patients
Raffaella 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-mRNA
Rosanna 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 disease
Omid Seidizadeh, Luciano Baronciani, Paola Colpani, et al.
Biophysical Journal
|
May 27, 2008
Mechanistic studies on ADAMTS13 catalysis
Enrico 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 study
Carlotta 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 afibrinogenemia
Rosanna 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 patients
Maria Teresa Pagliari, Luciano Baronciani, Chiara Cordiglieri, et al.
Page
of 61