Usefulness of the Total Thrombus-Formation Analysis System (T-TAS) in the diagnosis and characterization of von Willebrand disease von Daidone, V., Barbon, G., Cattini, M. G., Pontara, E., Romualdi, C., Di Pasquale, I., Hosokawa, K., Casonato, A.

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Von Willebrand factor propeptide makes it easy to identify the shorter Von Willebrand factor survival in patients with type 1 and type Vicenza von Willebrand disease von Sztukowska, M., Gallinaro, L., Cattini, M. G., Pontara, E., Sartorello, F., Daidone, V., Padrini, R., Pagnan, A., Casonato, A.

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Lupus anticoagulant identifies two distinct groups of patients with different antibody patterns von Pengo, V., Del Ross, T., Ruffatti, A., Bison, E., Cattini, M.G., Pontara, E., Testa, S., Legnani, C., Pozzi, N., Peterle, D., Acquasaliente, L., De Filippis, V., Denas, G.

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Thrombocytopenia in high‐risk patients with antiphospholipid syndrome von Pontara, E., Banzato, A., Bison, E., Cattini, M. G., Baroni, G., Denas, G., Calligaro, A., Marson, P., Tison, T., Ruffatti, A., Pengo, V.

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An in vitro model to mimic the thrombotic occlusion of small vessels in catastrophic antiphospholipid syndrome (CAPS) von Pontara, E, Cheng, C, Cattini, M G, Bison, E, Pelloso, M, Denas, G, Pengo, V

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Severe, recessive type 1 is a discrete form of von Willebrand disease: the lesson learned from the c.1534-3C>A von Willebrand factor mutation von Casonato, A, Cattini, M.G, Barbon, G, Daidone, V, Pontara, E

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Von Willebrand factor collagen binding activity in the diagnosis of von Willebrand disease: an alternative to ristocetin co‐factor activity? von Casonato, A., Pontara, E., Bertomoro, A., Sartorello, F., Cattini, M. G., Girolami, A.

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Venous thromboembolism in patients with Cushing’s syndrome: need of a careful investigation of the prothrombotic risk profile von Koutroumpi, S., Daidone, V., Sartori, M. T., Cattini, M. G., Albiger, N. M., Occhi, G., Ferasin, S., Frigo, A., Mantero, F., Casonato, A., Scaroni, C.

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Lack of multimer organization of von Willebrand factor in an acquired von Willebrand syndrome von Casonato, A., Pontara, E., Doria, A., Bertomoro, A., Cattini, M. G., Gambari, P. F., Girolami, A.

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Peripheral blood immune cells distribution in biopsy-proven myocarditis: etiology and prognostic correlates von Vicenzetto, C, Giordani, A S, Baritussio, A, Brigiari, G, Peloso Cattini, M G, Pontara, E, Bison, E, Tarantini, G, Gregori, D, Carturan, E, De Gaspari, M, Rizzo, S, Basso, C, Iliceto, S, Caforio, A L P

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Identifying Carriers of Type 2N von Willebrand Disease: Procedures and Significance von Casonato, A., Pontara, E., Sartorello, F., Cattini, M.G., Perutelli, P., Bertomoro, A., Gallinaro, L., Pagnan, A.

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von Willebrand factor abnormalities in aortic valve stenosis: Pathophysiology and impact on bleeding von Casonato, Alessandra, Sponga, Sandro, Pontara, Elena, Cattini, Maria Grazia, Basso, Cristina, Thiene, Gaetano, Cella, Giuseppe, Daidone, Viviana, Gerosa, Gino, Pagnan, Antonio

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Loss of cysteine 584 impairs the storage and release, but not the synthesis of von Willebrand factor von Daidone, Viviana, Barbon, Giovanni, Pontara, Elena, Cattini, Grazia M., Gallinaro, Lisa, Zampese, Enrico, Pizzo, Paola, Casonato, Alessandra

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Reduced survival of type 2B von Willebrand factor, irrespective of large multimer representation or thrombocytopenia von CASONATO, Alessandra, GALLINARO, Lisa, GRAZIA CATTINI, Maria, PONTARA, Elena, PADRINI, Roberto, BERTOMORO, Antonella, DAIDONE, Viviana, PAGNAN, Antonio

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C2362F mutation gives rise to an ADAMTS13-resistant von Willebrand factor von Casonato, Alessandra, Pontara, Elena, Battiston, Monica, Morpurgo, Margherita, Cattini, Maria Grazia, Casarin, Elisabetta, Saga, Giorgia, Daidone, Viviana, De Marco, Luigi

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Diagnosis and Follow-up of Thrombotic Thrombocytopenic Purpura by Means of von Willebrand Factor Collagen Binding Assay von Casonato, A., Fabris, F., Pontara, E., Cattini, M. G., Zocca, N., Gallinaro, L., Girolami, A., Pagnan, A.

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C2362F mutation gives rise to an ADAMTS13-resistant von Willebrand factor von A. Casonato, E. Pontara, M. Battiston, M. Morpurgo, M. G. Cattini, E. Casarin, G. Saga, V. Daidone, L. De Marco

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Combined hemophilia A and type 2N von Willebrand's disease : defect of both factor VIII level and factor VIII binding capacity of von Willebrand factor von CASONATO, Alessandra, PONTARA, Elena, SARTORELLO, Francesca, GEMMATI, Donato, CATTINI, Maria Grazia, GIROLAMI, Antonio

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Reduced von Willebrand factor survival in type Vicenza von Willebrand disease von Casonato, Alessandra, Pontara, Elena, Sartorello, Francesca, Cattini, Maria Grazia, Sartori, Maria Teresa, Padrini, Roberto, Girolami, Antonio

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An Arg760Cys mutation in the consensus sequence of the von Willebrand factor propeptide cleavage site is responsible for a new von Willebrand disease variant von Casonato, Alessandra, Sartorello, Francesca, Cattini, Maria Grazia, Pontara, Elena, Soldera, Carmen, Bertomoro, Antonella, Girolami, Antonio

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