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Thrombosis and Haemostasis|October 6, 1997
New coagulation factor V gene polymorphisms define a single and infrequent haplotype underlying the factor V Leiden mutation in Mediterranean populations and IndiansE Castoldi, B Lunghi, F Mingozzi, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|February 12, 1999
Phenotype and genotype expression in pseudohomozygous factor VLEIDEN : the need for phenotype analysisM Kalafatis, F Bernardi, P Simioni, et al.Haematologica|June 22, 2001
A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the Italian populationE Castoldi, B Lunghi, F Mingozzi, et al.Journal of Thrombosis and Haemostasis : JTH|July 23, 2003
Venous thromboembolism, oral contraceptives and high prothrombin levelsC Legnani, B Cosmi, L Valdrè, et al.Human Genetics|April 1, 1988
A HindIII RFLP and a gene lesion in the coagulation factor VIII geneF Bernardi, C Legnani, S Volinia, et al.Thrombosis and Haemostasis|February 24, 2001
Functional properties of factor V and factor Va encoded by the R2-geneL Hoekema, E Castoldi, G Tans, et al.Blood|August 15, 1997
A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotypeF Bernardi, E M Faioni, E Castoldi, et al.British Journal of Haematology|September 1, 1993
Study of a protein S gene polymorphism at DNA and mRNA level in a family with symptomatic protein S deficiencyG Marchetti, C Legnani, P Patracchini, et al.British Journal of Haematology|June 1, 1992
Rapid detection of a protein C gene mutation present in the asymptomatic and not in the thrombosis-prone lineageF Bernardi, P Patracchini, D Gemmati, et al.British Journal of Haematology|January 1, 1996
A novel mutation (Leu817Pro) causing type 2A von Willebrand diseaseD Gemmati, M L Serino, S Moratelli, et al.Pageof 44