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British Journal of Haematology|September 21, 2001
A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disordersE Castoldi, B Lunghi, F Mingozzi, et al.
The Journal of Laboratory and Clinical Medicine|January 10, 2001
Type 2M von Willebrand disease variant characterized by abnormal von willebrand factor multimerizationA Casonato, E Pontara, F Sartorello, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1983
In vitro stability studies of a Factor IX concentrate (Bebulin)R Dal Bo Zanon, R Gazzetta, G Patrassi, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1981
Improvement of platelet aggregation abnormalities in thrombocytosis after thrombocytopheresisF Fabris, M Belloni, A Casonato, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1983
Antithrombin III Padua: a "new" congenital antithrombin III abnormality with normal or near normal activity, normal antigen, abnormal migration and no thrombotic diseaseA Girolami, V Pengo, G Cappellato, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1985
The use of laser-nephelometry in evaluating fibrinogenaemia in patients with hepatocarcinoma and cirrhosisA Girolami, S Antico, V Pengo, et al.
Haematologia|January 1, 1987
A new family with congenital factor XIII deficiency showing a deficit of both subunit A and B. Type I factor XIII deficiencyM G Capellato, A R Lazzaro, F Marafioti, et al.
Blut|January 1, 1986
Associated von Willebrand disease as a possible cause of lack of thrombosis in an AT III abnormality (AT III Trento)A Girolami, M G Cappellato, M A Vicarioto, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 24, 1998
Congenital deficiencies and abnormalities of prothrombinA Girolami, L Scarano, G Saggiorato, et al.
Meat Science|November 9, 2011
Effect of forage to concentrate ratio on growth performance, and on carcass and meat quality of Podolian young bullsR Marino, M Albenzio, A Girolami, et al.
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