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Haemophilia : the Official Journal of the World Federation of Hemophilia|December 18, 2009
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia AV Bafunno, R Santacroce, M Chetta, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|May 12, 2016
The thrombin generation assay distinguishes inhibitor from non-inhibitor patients with severe haemophilia AM E Mancuso, V Chantarangkul, M Clerici, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|May 21, 2016
Low thrombin generation during major orthopaedic surgery fails to predict the bleeding risk in inhibitor patients treated with bypassing agentsM E Mancuso, V Chantarangkul, M Clerici, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|March 12, 2014
Management of orthopaedic surgery in rare bleeding disordersS M Siboni, E Biguzzi, G Pasta, et al.British Journal of Haematology|July 19, 2006
Prospective study on the behaviour of the metalloprotease ADAMTS13 and of von Willebrand factor after bone marrow transplantationF Peyvandi, S M Siboni, D Lambertenghi Deliliers, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|April 1, 1997
Gene polymorphisms predicting high plasma levels of coagulation and fibrinolysis proteins. A study in centenariansP M Mannucci, D Mari, G Merati, et al.Journal of Thrombosis and Haemostasis : JTH|June 4, 2015
Hepatic fibrinogen storage disease: identification of two novel mutations (p.Asp316Asn, fibrinogen Pisa and p.Gly366Ser, fibrinogen Beograd) impacting on the fibrinogen γ-moduleR Asselta, M Robusto, P Braidotti, et al.Blood|February 13, 2001
Abnormal secretion and function of recombinant human factor VII as the result of modification to a calcium binding site caused by a 15-base pair insertion in the F7 geneF Peyvandi, J A Carew, D J Perry, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|December 17, 2013
Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutationsM Borhany, H Handrkova, A Cairo, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|February 10, 2017
Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutationM S Badin, J K Iyer, M Chong, et al.Pageof 15