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Haematologica|April 10, 2010
Similar hypercoagulable state and thrombosis risk in type I and type III protein S-deficient individuals from mixed type I/III familiesElisabetta Castoldi, Lisbeth F A Maurissen, Daniela Tormene, et al.Thrombosis and Haemostasis|February 24, 2006
Protein S levels modulate the activated protein C resistance phenotype induced by elevated prothrombin levelsJeroen M Brugge, Guido Tans, Jan Rosing, et al.Thrombosis and Haemostasis|January 12, 2010
Thrombin generation as an intermediate phenotype for venous thrombosisOlivier Segers, René van van Oerle, Hugo ten ten Cate, et al.Blood|October 3, 2013
Antisense-based RNA therapy of factor V deficiency: in vitro and ex vivo rescue of a F5 deep-intronic splicing mutationFrancesca Nuzzo, Claudia Radu, Marco Baralle, et al.Thrombosis and Haemostasis|September 28, 2002
Reduced factor V concentration and altered FV1/FV2 ratio do not fully explain R2-associated APC-resistanceJosé W P Govers-Riemslag, Elisabetta Castoldi, Gerry A F Nicolaes, et al.Blood|February 21, 2004
Impaired APC cofactor activity of factor V plays a major role in the APC resistance associated with the factor V Leiden (R506Q) and R2 (H1299R) mutationsElisabetta Castoldi, Jeroen M Brugge, Gerry A F Nicolaes, et al.British Journal of Haematology|July 23, 2016
Endocytosis of exogenous factor V by ex-vivo differentiated megakaryocytes from patients with severe parahaemophiliaClaudia M Radu, Luca Spiezia, Cristiana Bulato, et al.Blood|September 5, 2008
Thrombin generation and activated protein C resistance in patients with essential thrombocythemia and polycythemia veraMarina Marchetti, Elisabetta Castoldi, Henri M H Spronk, et al.Blood|July 26, 2003
Coinheritance of Factor V (FV) Leiden enhances thrombin formation and is associated with a mild bleeding phenotype in patients homozygous for the FVII 9726+5G>A (FVII Lazio) mutationElisabetta Castoldi, Jose W P Govers-Riemslag, Mirko Pinotti, et al.Pageof 41