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Arteriosclerosis, Thrombosis, and Vascular Biology|December 31, 1997
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery diseaseP Ferraresi, G Marchetti, C Legnani, et al.Science & Justice : Journal of the Forensic Science Society|November 22, 2021
Blood and sperm traces on human hair. A study on preservation and detection after 3-month outdoor exposureG Caccia, A Cappella, E Castoldi, et al.Journal of Thrombosis and Haemostasis : JTH|February 18, 2017
New functional assays to selectively quantify the activated protein C- and tissue factor pathway inhibitor-cofactor activities of protein S in plasmaN A Alshaikh, J Rosing, M C L G D Thomassen, et al.Journal of Thrombosis and Haemostasis : JTH|April 28, 2007
Differential effects of high prothrombin levels on thrombin generation depending on the cause of the hyperprothrombinemiaE Castoldi, P Simioni, D Tormene, et al.Journal of Thrombosis and Haemostasis : JTH|April 20, 2016
Identification and functional characterization of a novel F5 mutation (Ala512Val, FVB onn ) associated with activated protein C resistanceB Pezeshkpoor, E Castoldi, A Mahler, et al.Journal of Thrombosis and Haemostasis : JTH|December 20, 2005
Expression of the normal factor V allele modulates the APC resistance phenotype in heterozygous carriers of the factor V Leiden mutationJ M Brugge, P Simioni, F Bernardi, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|December 4, 2014
Characterization of an apparently synonymous F5 mutation causing aberrant splicing and factor V deficiencyF Nuzzo, C Bulato, B I Nielsen, et al.Thrombosis and Haemostasis|October 6, 1998
Molecular bases of pseudo-homozygous APC resistance: the compound heterozygosity for FV R506Q and a FV null mutation results in the exclusive presence of FV Leiden molecules in plasmaE Castoldi, M Kalafatis, B Lunghi, et al.Journal of Thrombosis and Haemostasis : JTH|June 25, 2005
The factor V Glu1608Lys mutation is recurrent in familial thrombophiliaB Lunghi, D Scanavini, E Castoldi, et al.Journal of Thrombosis and Haemostasis : JTH|November 9, 2007
Coagulation factors and the protein C system as determinants of thrombin generation in a normal populationA W J H Dielis, E Castoldi, H M H Spronk, et al.Pageof 4