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European Heart Journal|June 19, 2002
Venous thromboembolism in young women; role of thrombophilic mutations and oral contraceptive useC Legnani, G Palareti, G Guazzaloca, 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.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|January 1, 1994
Glutathione metabolism in heart and liver of the aging ratM Stio, T Iantomasi, F Favilli, et al.
Neurobiology of Aging|July 1, 1994
Relationship between age and GSH metabolism in synaptosomes of rat cerebral cortexF Favilli, T Iantomasi, P Marraccini, et al.
The European Respiratory Journal|January 11, 2005
Different lung responses to cigarette smoke in two strains of mice sensitive to oxidantsB Bartalesi, E Cavarra, S Fineschi, et al.
Thrombosis and Haemostasis|October 1, 1996
A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjectsF Bernardi, C Legnani, F Micheletti, et al.
Blood|August 15, 2000
Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic familyE Castoldi, P Simioni, M Kalafatis, 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|January 1, 1996
A novel mutation (Leu817Pro) causing type 2A von Willebrand diseaseD Gemmati, M L Serino, S Moratelli, et al.
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.
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