Alessandra Casonato
Alessandra Casonato
MD, Dept. of Cardiologic
Thoracic and Vascular Sciences
E-mail:
Name/email consistency: high
- von Willebrand factor abnormalities in aortic valve stenosis: Pathophysiology and impact on bleeding. Casonato, A., Sponga, S., Pontara, E., Cattini, M.G., Basso, C., Thiene, G., Cella, G., Daidone, V., Gerosa, G., Pagnan, A. Thromb. Haemost. (2011)
- Reduced survival of type 2B von Willebrand factor, irrespective of large multimer representation or thrombocytopenia. Casonato, A., Gallinaro, L., Cattini, M.G., Pontara, E., Padrini, R., Bertomoro, A., Daidone, V., Pagnan, A. Haematologica (2010)
- Type 1 von Willebrand disease due to reduced von Willebrand factor synthesis and/or survival: observations from a case series. Casonato, A., Gallinaro, L., Cattini, M.G., Sartorello, F., Pontara, E., Padrini, R., Bertomoro, A., Daidone, V., Pagnan, A. Transl. Res (2010)
- Hypercortisolism and pregnancy upregulate von Willebrand factor through different mechanisms: report on a pregnant patient with Cushing's syndrome. Casonato, A., Daidone, V., Pontara, E., Albiger, N., Cattini, M.G., Scaroni, C. Blood Coagul. Fibrinolysis (2010)
- Polymorphisms in von Willebrand factor gene promoter influence the glucocorticoid-induced increase in von Willebrand factor: the lesson learned from Cushing syndrome. Casonato, A., Daidone, V., Sartorello, F., Albiger, N., Romualdi, C., Mantero, F., Pagnan, A., Scaroni, C. Br. J. Haematol. (2008)
- Identifying carriers of type 2N von Willebrand disease: procedures and significance. Casonato, A., Pontara, E., Sartorello, F., Cattini, M.G., Perutelli, P., Bertomoro, A., Gallinaro, L., Pagnan, A. Clin. Appl. Thromb. Hemost. (2007)
- A novel von Willebrand factor mutation (I1372S) associated with type 2B-like von Willebrand disease: an elusive phenotype and a difficult diagnosis. Casonato, A., Sartorello, F., Pontara, E., Gallinaro, L., Bertomoro, A., Grazia Cattini, M., Daidone, V., Szukowska, M., Pagnan, A. Thromb. Haemost. (2007)
- Altered von Willebrand factor subunit proteolysis and multimer processing associated with the Cys2362Phe mutation in the B2 domain. Casonato, A., De Marco, L., Gallinaro, L., Sztukowska, M., Mazzuccato, M., Battiston, M., Pagnan, A., Ruggeri, Z.M. Thromb. Haemost. (2007)
- Identifying type Vicenza von Willebrand disease. Casonato, A., Pontara, E., Sartorello, F., Cattini, M.G., Gallinaro, L., Bertomoro, A., Rosato, A., Padrini, R., Pagnan, A. J. Lab. Clin. Med. (2006)
- Diagnosis and follow-up of thrombotic thrombocytopenic purpura by means of von Willebrand factor collagen binding assay. Casonato, A., Fabris, F., Pontara, E., Cattini, M.G., Zocca, N., Gallinaro, L., Girolami, A., Pagnan, A. Clin. Appl. Thromb. Hemost. (2006)
- A new L1446P mutation is responsible for impaired von Willebrand factor synthesis, structure, and function. Casonato, A., Cattini, M.G., Soldera, C., Marcato, S., Sartorello, F., Pontara, E., Pagnan, A. J. Lab. Clin. Med. (2004)
- An Arg760Cys mutation in the consensus sequence of the von Willebrand factor propeptide cleavage site is responsible for a new von Willebrand disease variant. Casonato, A., Sartorello, F., Cattini, M.G., Pontara, E., Soldera, C., Bertomoro, A., Girolami, A. Blood (2003)
- Fainting induces an acute increase in the concentration of plasma factor VIII and von Willebrand factor. Casonato, A., Pontara, E., Bertomoro, A., Cattini, M.G., Soldera, C., Girolami, A. Haematologica (2003)
- Reduced von Willebrand factor survival in type Vicenza von Willebrand disease. Casonato, A., Pontara, E., Sartorello, F., Cattini, M.G., Sartori, M.T., Padrini, R., Girolami, A. Blood (2002)
- Lack of multimer organization of von Willebrand factor in an acquired von Willebrand syndrome. Casonato, A., Pontara, E., Doria, A., Bertomoro, A., Cattini, M.G., Gambari, P.F., Girolami, A. Br. J. Haematol. (2002)
