BARBON, GIOVANNI
BARBON, GIOVANNI
ARMC5 mutation analysis in patients with primary aldosteronism and bilateral adrenal lesions
2016 Mulatero, P; Schiavi, Francesca; Williams, T. A.; Monticone, S.; Barbon, Giovanni; Opocher, Giuseppe; Fallo, Francesco
Loss of cysteine 584 impairs the storage and release, but not the synthesis of von Willebrand factor
2014 Daidone, Viviana; Barbon, Giovanni; Pontara, Elena; Cattini, Mg; Gallinaro, L; Zampese, Enrico; Pizzo, Paola; Casonato, Sandra
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
2015 Casonato, Sandra; PELOSO CATTINI, MARIA GRAZIA; Barbon, Giovanni; Daidone, Viviana; Pontara, Elena
Spontaneous hemarthrosis in combined Glanzmann thrombasthenia and type 2N von Willebrand disease.
2014 Pontara, Elena; Gresele, Paolo; PELOSO CATTINI, MARIA GRAZIA; Daidone, Viviana; Barbon, Giovanni; Girolami, Antonio; Zanonato, Elisa; Casonato, Sandra
The p.R1819_C1948delinsS mutation makes von Willebrand factor ADAMTS13-resistant and reduces its collagen-binding capacity
2015 Daidone, Viviana; Saga, Giorgia; Barbon, Giovanni; Pontara, Elena; PELOSO CATTINI, MARIA GRAZIA; Morpurgo, Margherita; Zanotti, Giuseppe; Casonato, Sandra
Usefulness of the Total Thrombus-Formation Analysis System (T-TAS) in the diagnosis and characterization of von Willebrand disease
2016 Daidone, Viviana; Barbon, Giovanni; PELOSO CATTINI, MARIA GRAZIA; Pontara, Elena; Romualdi, Chiara; DI PASQUALE, Irene; Hosokawa, K; Casonato, Sandra