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British Journal of Haematology|August 1, 1995
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domainG Marchetti, G Castaman, M Pinotti, et al.
Journal of Thrombosis and Haemostasis : JTH|March 5, 2008
Vitamin K-induced modification of coagulation phenotype in VKORC1 homozygous deficiencyG Marchetti, P Caruso, B Lunghi, et al.
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.
British Journal of Haematology|March 1, 1990
Characterization of polymorphic markers in the von Willebrand factor gene and pseudogeneF Bernardi, G Marchetti, A Casonato, et al.
Human Mutation|January 1, 1996
Mutation pattern in clinically asymptomatic coagulation factor VII deficiencyF Bernardi, G Castaman, M Pinotti, 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.
Blood|May 29, 2000
Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studiesM Pinotti, R Toso, D Girelli, 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.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 31, 1997
Hyperhomocyst(e)inemia and a common methylenetetrahydrofolate reductase mutation (Ala223Val MTHFR) in patients with inherited thrombophilic coagulation defectsC Legnani, G Palareti, F Grauso, et al.
The New England Journal of Medicine|September 14, 2000
Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery diseaseD Girelli, C Russo, P Ferraresi, et al.
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