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British Journal of Haematology|December 19, 1998
Two novel mutations (Pro864His, Val867Glu) causing type 2A von Willebrand disease and affecting a single restriction site in exon 28F Bernardi, A Casonato, G Marchetti, et al.
Haemostasis|October 31, 2001
Coexistence of factor V G1691A and factor II G20210A gene mutations in a thrombotic family is associated with recurrence and early onset of venous thrombosisD Gemmati, M L Serino, S Moratelli, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 11, 1998
Coexistence of antithrombin deficiency, factor V Leiden and hyperhomocysteinemia in a thrombotic familyD Gemmati, M L Serino, S Moratelli, 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.
Hematologic Pathology|January 1, 1990
Direct detection of a missense mutation causing severe hemophilia A by PCR amplification and fluorescence scanningG Marchetti, D Gemmati, P Patracchini, et al.
Blood|February 1, 1990
A de novo and heterozygous gene deletion causing a variant of von Willebrand diseaseF Bernardi, G Marchetti, S Guerra, et al.
Osteoarthritis and Cartilage|October 3, 2002
High doses of glucosamine-HCl have detrimental effects on bovine articular cartilage explants cultured in vitroM de Mattei, A Pellati, M Pasello, 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|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.
Osteoarthritis and Cartilage|August 15, 2006
Proteoglycan synthesis in bovine articular cartilage explants exposed to different low-frequency low-energy pulsed electromagnetic fieldsM De Mattei, M Fini, S Setti, et al.
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