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Haemophilia : the Official Journal of the World Federation of Hemophilia|July 13, 2006
Arterial and venous thrombosis in rare congenital bleeding disorders: a critical reviewA Girolami, E Ruzzon, F Tezza, et al.
Journal of Thrombosis and Thrombolysis|August 13, 2004
The occasional venous thromboses seen in patients with severe (homozygous) FXII deficiency are probably due to associated risk factors: a study of prevalence in 21 patients and review of the literatureA Girolami, M L Randi, S Gavasso, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 24, 1999
Failure of soluble fibrin polymers in the diagnosis of clinically suspected deep venous thrombosisL Scarano, P Prandoni, S Gavasso, et al.
The Journal of Laboratory and Clinical Medicine|February 1, 1997
Abnormal collagen binding activity of 2A von Willebrand factor: evidence that the defect depends only on the lack of large multimersA Casonato, E Pontara, A Bertomoro, et al.
Acta Haematologica|April 29, 2010
Thrombotic events in patients with congenital prekallikrein deficiency: a critical evaluation of all reported casesA Girolami, E Allemand, I Bertozzi, et al.
Meat Science|November 9, 2011
Fatty acid profile, cholesterol content and tenderness of meat from Podolian young bullsG F Cifuni, F Napolitano, A M Riviezzi, et al.
Meat Science|November 9, 2011
Effect of artificial rearing on lamb welfare and meat qualityF Napolitano, G F Cifuni, C Pacelli, et al.
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
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.
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