Sfoglia per Autore
No von Willebrand factor domains other than A1 are involved in type 2B von Willebrand disease: what the p.R924Q and p.A2178S variants teach us
2023 Casonato, Sandra; Gianesello, Lisa; Regazzo, Daniela; Galletta, Eva; Daidone, Viviana
The Lesson Learned from the New c.2547-1G>T Mutation Combined with p.R854Q: When a Type 2N Mutation Reveals a Quantitative von Willebrand Factor Defect
2022 Casonato, Alessandra; Cozzi, Maria Rita; Ferrari, Silvia; Rubin, Beatrice; Gianesello, Lisa; De Marco, Luigi; Daidone, Viviana
The lesson learned from the new c.2547-1G>T mutation combined with p.R854Q:when a type 2N mutation reveals a quantitative von Willebrand factor defect.
2022 Casonato, A; Cozzi, Mrc; Ferrari, S; Rubin, B; Gianesello, L; De Marco, L; Daidone, V.
Von Willebrand disease type Vicenza: In search of a classification for the archetype of reduced von Willebrand factor survival
2021 Casonato, S; Galletta, E; Galvanin, F; Daidone, V
Acquired von Willebrand Syndrome Hiding Inherited von Willebrand Disease Can Explain Severe Bleeding in Patients With Aortic Stenosis.
2020 Casonato, A; Galletta, E; Cella, G; Barbon, G; Daidone, V.
Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC
2019 Gresele, P.; Orsini, S.; Noris, P.; Falcinelli, E.; Alessi, M. C.; Bury, L.; Borhany, M.; Santoro, C.; Glembotsky, A. C.; Cid, A. R.; Tosetto, A.; De Candia, E.; Fontana, P.; Guglielmini, G.; Pecci, A.; Heller, P. G.; Rodorigo, G.; Lammle, B.; Trinchero, A.; Paolo, R.; Ferrari, S.; Rancitelli, D.; Stolinski, A.; Arulselvan, A.; Lassandro, G.; Luceros, A. S.; Jandrot-Perrus, M.; Kunishima, S.; Rivera Pozo, J.; Lordkipanidze, M.; Melazzini, F.; Falaise, C.; Casonato, A.; Podda, G.; Kannan, M.; Jurk, K.; Sevivas, T.; Castaman, G.; Grandone, E.; Fiore, M.; Zuniga, P.; Henskens, Y.; Miyazaki, K.; Dupuis, A.; Hayward, C.; Zaninetti, C.; Abid, M.; Ferrara, G.; Mazzucconi, M. G.; Tagariello, G.; James, P.; Fabris, F.; Russo, A.; Bermejo, N.; Napolitano, M.; Curnow, J.; Vasiliki, G.; Zieger, B.; Fedor, M.; Chitlur, M.; Lambert, M.; Barcella, L.; Cosmi, B.; Giordano, P.; Porri, C.; Eker, I.; Morel-Kopp, M. -C.; Deckmyn, H.; Frelinger, A. L.; Harrison, P.; Mezzano, D.; Mumford, A. D.
Cryptic noncanonical splice site activation is part of the mechanism that abolishes multimer organization in the c.2269_2270del von Willebrand factor
2019 Daidone, Viviana; Galletta, Eva; De Marco, Luigi; Casonato, Alessandra
A framework for the optimal design of a minimum set of clinical trials to characterize von Willebrand disease
2019 Taverna, B; Cason ato, A; Bezzo, F; Galvanin, F
A framework for the optimal design of a minimum set of clinical trials to characterize von Willebrand disease
2019 Taverna, B.; Casonato, A.; Bezzo, F.; Galvanin, F.
The elusive and heterogeneous pattern of type 2M von Willebrand disease: A diagnostic challenge
2018 Casonato, Alessandra; Galletta, Eva; Daidone, Viviana
Type 3 von Willebrand disease mistaken for moderate haemophilia A: a lesson still to be learned
2018 Galletta, E; Daidone, V; Zanon, E; Casonato, S
Towards the optimal design of a minimum set of clinical trials for the identification and characterization of VWD
2018 Taverna, Beatrice; Casonato, Alessandra; Bezzo, Fabrizio; Galvanin, Federico
Type 1 von Willebrand disease due to a vicinal cysteine loss (p.C524Y) disclosed after a thrombotic episode
2018 Daidone, Viviana; Galletta, Eva; Casonato, Alessandra
A model-based protocol for the diagnosis of von Willebrand disease
2018 Castaldello, Christopher; Galvanin, Federico; Casonato, Alessandra; Padrini, Roberto; Barolo, Massimiliano; Bezzo, Fabrizio
Type 2N von Willebrand disease: Characterization and diagnostic difficulties
2018 Casonato, A.; Galletta, E.; Sarolo, L.; Daidone, V.
A Mechanistic Model to Quantify von Willebrand Factor Release, Survival and Proteolysis in Patients with von Willebrand Disease
2018 Ferrari, Myriam; Galvanin, Federico; Barolo, Massimiliano; Daidone, Viviana; Padrini, Roberto; Bezzo, Fabrizio; Casonato, Alessandra
Haemostatic patterns and bleeding scores of a genetically characterised Italian family with combined haemophilia A and type 1 von Willebrand disease
2017 Daidone, Viviana; Pontara, Elena; Boscaro, Francesca; PELOSO CATTINI, MARIA GRAZIA; Milan, Marta; Casonato, Sandra
Towards the optimal design of a minimal set of clinical tests for the identification and characterization of von Willebrand disease
2017 Taverna, B.; Casonato, A.; Bezzo, F.; Galvanin, F.
Two novel ITGA2B mutations in a Glanzmann thrombasthaenia family associated with different platelet phenotypic expression
2017 Daidone, Viviana; Bury, Loredana; Milan, Marta; Galletta, Eva; Gresele, Paolo; Casonato, Sandra
Type 2B von Willebrand disease with or without large multimers: A distinction of the two sides of the disorder is long overdue
2017 Casonato, Alessandra; Daidone, Viviana; Galletta, Eva; Bertomoro, Antonella
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