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Haematologica|June 11, 2026
Major adverse cardiovascular events in immune-mediated thrombotic thrombocytopenic purpura during clinical remissionPasquale Agosti, Federico Boggio, Ilaria Mancini, et al.
Thrombosis Research|April 5, 2016
Duration of oral contraceptive use and the risk of venous thromboembolism. A case-control studyIda Martinelli, Alberto Maino, Maria Abbattista, et al.
Clinical Chemistry and Laboratory Medicine|September 6, 2020
Emicizumab, the factor VIII mimetic bi-specific monoclonal antibody and its measurement in plasmaArmando Tripodi, Veena Chantarangkul, Cristina Novembrino, et al.
Blood Cells, Molecules & Diseases|August 5, 2008
Congenital hypofibrinogenemia: characterization of two missense mutations affecting fibrinogen assembly and secretionManuela Platè, Rosanna Asselta, Silvia Spena, et al.
Research and Practice in Thrombosis and Haemostasis|May 22, 2023
A comparative study in patients with type 2 von Willebrand disease using 4 different platelet-dependent von Willebrand factor assaysPaola Colpani, Luciano Baronciani, Francesca Stufano, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 13, 2008
Rotational thromboelastography for monitoring of fibrinogen concentrate therapy in fibrinogen deficiencyUwe Kalina, Hans-Arnold Stöhr, Heike Bickhard, et al.
Experimental Hematology & Oncology|June 14, 2014
Salvage therapy with high dose Intravenous Immunoglobulins in acquired Von Willebrand Syndrome and unresponsive severe intestinal bleedingMassimo Cugno, Alberto Tedeschi, Simona Maria Siboni, et al.
Rheumatology and Therapy|August 10, 2022
Successful Chemical Synovectomy in a Patient with Acquired von Willebrand Syndrome with Chronic Synovitis Due to Recurrent Knee Hemarthrosis: A Case ReportRoberta Gualtierotti, Claudio De Magistris, Eugenia Biguzzi, et al.
Blood Cells, Molecules & Diseases|May 10, 2003
Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patientsLuciano Baronciani, Giovanna Cozzi, Maria Teresa Canciani, et al.
Human Mutation|December 26, 2003
Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiencyFlora Peyvandi, Liliana Tagliabue, Marzia Menegatti, et al.
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