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Thrombosis and Haemostasis|September 6, 2006
Initial treatment of venous thromboembolismCecilia Becattini, Giancarlo Agnelli, Joseph Emmerich, et al.
The American Journal of Gastroenterology|September 1, 2005
Thrombosis in inflammatory bowel diseases: role of inherited thrombophiliaLuisa Spina, Simone Saibeni, Tullia Battaglioli, et al.
European Journal of Clinical Investigation|July 30, 2015
Frequency of the p.Gly262Asp mutation in congenital Factor X deficiencySerdar Epcacan, Marzia Menegatti, Sinan Akbayram, et al.
Haematologica|March 8, 2005
Homozygosity for a Thr575Met missense mutation in the catalytic domain associated with factor XI deficiencyMyrna Germanos-Haddad, Philippe de Moerloose, Françoise Boehlen, et al.
Frontiers in Medicine|April 22, 2024
Gender equity in hemophilia: need for healthcare, familial, and societal advocacyRoberta Gualtierotti, Isabella Garagiola, Mimosa Mortarino, et al.
Research and Practice in Thrombosis and Haemostasis|July 9, 2026
Differential expression of miR-128 in memory T cells of patients with severe hemophilia A with and without inhibitorsSilvia Spena, Andrea Cairo, Emanuela Pappalardo, et al.
British Journal of Haematology|April 11, 2016
Pregnancy loss and risk of ischaemic stroke and myocardial infarctionAlberto Maino, Bob Siegerink, Ale Algra, et al.
Journal of Thrombosis and Haemostasis : JTH|February 15, 2019
Risk of diagnostic delay in congenital thrombotic thrombocytopenic purpuraBarbara Ferrari, Andrea Cairo, Maria Teresa Pagliari, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|February 9, 2013
Comparison of thrombin generation assay with conventional coagulation tests in evaluation of bleeding risk in patients with rare bleeding disordersOmid R Zekavat, Sezaneh Haghpanah, Javad Dehghani, et al.
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