Search Results - "CASONATO, A."

Type 2N von Willebrand disease: Characterization and diagnostic difficulties by Casonato, A., Galletta, E., Sarolo, L., Daidone, V.

“…Introduction An abnormal factor VIII (FVIII) binding capacity of von Willebrand factor (VWF) identifies type 2N von Willebrand disease (VWD). Type 2N VWD…”
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Construct Validity and Responsiveness of Performance-based Tests in Individuals With Knee Osteoarthritis by Ramalho, Rebecca B., Casonato, Natália A., Montilha, Vinicius B., Chaves, Thais C., Mattiello, Stela M., Selistre, Luiz F.A.

“…To assess the construct validity and responsiveness of 3 performance-based tests in individuals with knee osteoarthritis (KOA). This study has a prospective…”
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A framework for the optimal design of a minimum set of clinical trials to characterize von Willebrand disease by Taverna, B., Casonato, A., Bezzo, F., Galvanin, F.

“…•Kinetic models have been recently proposed to help in the diagnosis and characterization of von Willebrand disease (VWD).•The complexity of these kinetic…”
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PERSONALISING HIGH TIBIAL OSTEOTOMY: ‘IDEAL’ PRECLINICAL STAGE EVALUATION OF TOKA® - A NOVEL PATIENT SPECIFIC 3D PRINTED SYSTEM by Mathews, J., MacLeod, A., Toms, A., Gill, R., Casonato, A., Mandalia, V.

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

“…Introduction The heterogeneity of von Willebrand disease (VWD) makes its diagnosis a difficult task. Methods We report here on the usefulness of a…”
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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 by Casonato, A, Cattini, M.G, Barbon, G, Daidone, V, Pontara, E

“…Abstract Type 1 von Willebrand disease (VWD) is transmitted mainly as a dominant trait - especially in forms involving von Willebrand factor (VWF) levels below…”
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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 by Sztukowska, M., Gallinaro, L., Cattini, M. G., Pontara, E., Sartorello, F., Daidone, V., Padrini, R., Pagnan, A., Casonato, A.

“…Summary Reduced von Willebrand factor (VWF) half‐life has been suggested as a new pathogenic mechanism in von Willebrand disease (VWD). The usefulness of VWF…”
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Venous thromboembolism in patients with Cushing’s syndrome: need of a careful investigation of the prothrombotic risk profile by 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.

“…A high incidence of venous thromboembolic (VTE) complications has been reported in Cushing’s syndrome (CS), mostly post-operatively and attributable to…”
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Arterial and venous thrombosis in patients with von Willebrand's disease: a critical review of the literature by Girolami, A, Tezza, F, Scapin, M, Vettore, S, Casonato, A

“…All patients with von Willebrand's disease (vWD) who showed an arterial or venous thrombosis and were reported in the literature have been evaluated. 11…”
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Uneventful coronary artery bypass surgery without prophylactic replacement therapy in a patient with a novel heterozygous FVII gene deletion by GALLINARO, L., CASONATO, A., VIANELLO, F., FADIN, M., CELLA, G.

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Optimal design of infusion tests for the identification of physiological models of acquired von Willebrand syndrome by Galvanin, F., Galletta, E., Bertomoro, A., Daidone, V., Casonato, A.

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Identifying carriers of type 2N von Willebrand disease: procedures and significance by Casonato, A, Pontara, E, Sartorello, F, Cattini, M G, Perutelli, P, Bertomoro, A, Gallinaro, L, Pagnan, A

“…The defective FVIII carrier function of von Willebrand factor (VWF) identifies type 2N von Willebrand disease (VWD), a variant with a pattern resembling…”
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Abnormalities of von Willebrand factor are also part of the prothrombotic state of Cushing's syndrome by Casonato, A, Pontara, E, Boscaro, M, Sonino, N, Sartorello, F, Ferasin, S, Girolami, A

“…Glucocorticoids are known to increase plasma concentrations of factor VIII (FVIII) and von Willebrand factor (vWF), and their administration is associated with…”
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Von Willebrand factor collagen binding activity in the diagnosis of von Willebrand disease: an alternative to ristocetin co‐factor activity? by Casonato, A., Pontara, E., Bertomoro, A., Sartorello, F., Cattini, M. G., Girolami, A.

“…The capability of von Willebrand factor (VWF) to bind platelet glycoprotein Ib (GPIb) and promote platelet plug formation is currently evaluated in vitro using…”
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Biochemical markers of endothelial activation in primary hyperparathyroidism by Fallo, F, Cella, G, Casonato, A, Ermani, M, Vettor, R, Zanella, S, Lumachi, F

“…Patients with primary hyperparathyroidism (PHPT) have impaired vasodilation both dependent and independent of endothelium. The aims of our study were to…”
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Post-DDAVP thrombocytopenia in type 2B von Willebrand disease is not associated with platelet consumption: failure to demonstrate glycocalicin increase or platelet activation by Casonato, A, Steffan, A, Pontara, E, Zucchetto, A, Rossi, C, De Marco, L, Girolami, A

“…Thrombocytopenia is frequently reported in type 2B von Willebrand disease (vWD), and thought to be related to the abnormally high affinity of 2B von Willebrand…”
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Early transfusion of factor VIII/von Willebrand factor concentrates seems to be effective in the treatment of gatrointestinal bleeding in patients with von Willebrand type III disease by Zanon, E., Vianello, F., Casonato, A., Girolami, A.

“…The association between gastrointestinal angiodysplasia and von Willebrand disease was reported 30 years ago. The clinical course of patients with von…”
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EDTA dependent pseudothrombocytopenia caused by antibodies against the cytoadhesive receptor of platelet gpIIB-IIIA by Casonato, A, Bertomoro, A, Pontara, E, Dannhauser, D, Lazzaro, A R, Girolami, A

“…AIMS--To clarify the mechanisms involved in the development of EDTA dependent pseudothrombocytopenia, particularly the platelet receptors. METHODS--Platelets…”
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Lack of multimer organization of von Willebrand factor in an acquired von Willebrand syndrome by Casonato, A., Pontara, E., Doria, A., Bertomoro, A., Cattini, M. G., Gambari, P. F., Girolami, A.

“…We report a case of acquired von Willebrand syndrome (AVWS) in a 20‐year‐old‐woman with systemic lupus erythematosus, in whom severe bleeding complications…”
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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 by CASONATO, Alessandra, PONTARA, Elena, SARTORELLO, Francesca, GEMMATI, Donato, CATTINI, Maria Grazia, GIROLAMI, Antonio

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