Type 2B von Willebrand disease with or without large multimers: A distinction of the two sides of the disorder is long overdue by Casonato, Alessandra, Daidone, Viviana, Galletta, Eva, Bertomoro, Antonella

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Cryptic non-canonical splice site activation is part of the mechanism that abolishes multimer organization in the c.2269_2270del von Willebrand factor by Daidone, Viviana, Galletta, Eva, De Marco, Luigi, Casonato, Alessandra

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A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factor by Gallinaro, Lisa, Cattini, Maria Grazia, Sztukowska, Maryta, Padrini, Roberto, Sartorello, Francesca, Pontara, Elena, Bertomoro, Antonella, Daidone, Viviana, Pagnan, Antonio, Casonato, Alessandra

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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 by Casonato, Alessandra, Gianesello, Lisa, Regazzo, Daniela, Galletta, Eva, Daidone, Viviana

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Diagnosis and complications of Cushing's disease: gender-related differences by Zilio, Marialuisa, Barbot, Mattia, Ceccato, Filippo, Camozzi, Valentina, Bilora, Franca, Casonato, Alessandra, Frigo, Anna Chiara, Albiger, Nora, Daidone, Viviana, Mazzai, Linda, Mantero, Franco, Scaroni, Carla

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Diagnostic Value of Measuring Platelet Von Willebrand Factor in Von Willebrand Disease by Casonato, Alessandra, Cattini, Maria Grazia, Daidone, Viviana, Pontara, Elena, Bertomoro, Antonella, Prandoni, Paolo

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Von Willebrand disease type Vicenza: In search of a classification for the archetype of reduced von Willebrand factor survival by Casonato, Alessandra, Galletta, Eva, Galvanin, Federico, Daidone, Viviana

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Coagulation activation in children with sickle cell disease is associated with cerebral small vessel vasculopathy by Colombatti, Raffaella, De Bon, Emiliano, Bertomoro, Antonella, Casonato, Alessandra, Pontara, Elena, Omenetto, Elisabetta, Saggiorato, Graziella, Steffan, Agostino, Damian, Tamara, Cella, Giuseppe, Teso, Simone, Manara, Renzo, Rampazzo, Patrizia, Meneghetti, Giorgio, Basso, Giuseppe, Sartori, Maria Teresa, Sainati, Laura

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

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An apparently silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand disease by DAIDONE, Viviana, GALLINARO, Lisa, GRAZIA CATTINI, Maria, PONTARA, Elena, BERTOMORO, Antonella, PAGNAN, Antonio, CASONATO, Alessandra

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A common ancestor more than 10,000 years old for patients with R854Q-related type 2N von Willebrand's disease in Italy by Casonato, Alessandra, Daidone, Viviana, Barbon, Giovanni, Pontara, Elena, Di Pasquale, Irene, Gallinaro, Lisa, Marullo, Letizia, Bertorelle, Giorgio

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Polymorphisms in von Willebrand factor gene promoter influence the glucocorticoid‐induced increase in von Willebrand factor: the lesson learned from Cushing syndrome by Casonato, Alessandra, Daidone, Viviana, Sartorello, Francesca, Albiger, Nora, Romualdi, Chiara, Mantero, Franco, Pagnan, Antonio, Scaroni, Carla

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Acquired von Willebrand syndrome in patients with monoclonal gammopathy of undetermined significance investigated using a mechanistic approach by Galletta, Eva, Galvanin, Federico, Bertomoro, Antonella, Daidone, Viviana, Casonato, Alessandra

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Type 1 von Willebrand disease due to a vicinal cysteine loss (p.C524Y) disclosed after a thrombotic episode by Daidone, Viviana, Galletta, Eva, Casonato, Alessandra

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The elusive and heterogeneous pattern of type 2M von Willebrand disease: A diagnostic challenge by Casonato, Alessandra, Galletta, Eva, Daidone, Viviana

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Validation of the ISTH/SSC bleeding assessment tool for inherited platelet disorders: A communication from the Platelet Physiology SSC by Gresele, Paolo, Orsini, Sara, Noris, Patrizia, Falcinelli, Emanuela, Alessi, Marie Christine, Bury, Loredana, Borhany, Munira, Santoro, Cristina, Glembotsky, Ana C., Cid, Ana Rosa, Tosetto, Alberto, De Candia, Erica, Fontana, Pierre, Guglielmini, Giuseppe, Pecci, Alessandro, Heller, Paula G., Rodorigo, Giuseppina, Lammle, Bernhard, Trinchero, Alice, Paolo, Radossi, Ferrari, Silvia, Rancitelli, Davide, Stolinski, Amy, Arulselvan, Abinaya, Lassandro, Giuseppe, Luceros, Analia Sanchez, Jandrot‐Perrus, Martine, Kunishima, Shinji, Rivera Pozo, José, Lordkipanidzé, Marie, Melazzini, Federica, Falaise, Céline, Casonato, Alessandra, Podda, Gianmarco, Kannan, Meganathan, Jurk, Kerstin, Sevivas, Teresa, Castaman, Giancarlo, Grandone, Elvira, Fiore, Mathieu, Zuniga, Pamela, Henskens, Yvonne, Miyazaki, Koji, Dupuis, Arnaud, Hayward, Catherine, Zaninetti, Carlo, Abid, Madiha, Ferrara, Grazia, Mazzucconi, Maria Gabriella, Tagariello, Giuseppe, James, Paula, Fabris, Fabrizio, Russo, Alexandra, Bermejo, Nuria, Napolitano, Mariasanta, Curnow, Jennifer, Vasiliki, Gkalea, Zieger, Barbara, Fedor, Marian, Chitlur, Meera, Lambert, Michele, Barcella, Luca, Cosmi, Benilde, Giordano, Paola, Porri, Claudia, Eker, Ibrahim, Morel‐Kopp, Marie‐Christine, Deckmyn, Hans, Frelinger, Andrew L., Harrison, Paul, Mezzano, Diego, Mumford, Andrew D.

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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 by Casonato, Alessandra, Sartorello, Francesca, Cattini, Maria Grazia, Pontara, Elena, Soldera, Carmen, Bertomoro, Antonella, Girolami, Antonio

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Early‐onset indicators of a hypercoagulable state and clinical complications in a cohort of children with sickle cell trait by Reggiani, Giulia, Boaro, Maria Paola, Menzato, Federica, De Bon, Emiliano, Bertomoro, Antonella, Casonato, Alessandra, Lucente, Fabrizio, Fortino, Cecilia, Sartori, MariaTeresa, Steffan, Agostino, Martella, Maddalena, D'Agnolo, Mirco, Sainati, Laura, Colombatti, Raffaella

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The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology by Gresele, Paolo, Falcinelli, Emanuela, Bury, Loredana, Pecci, Alessandro, Alessi, Marie‐Christine, Borhany, Munira, Heller, Paula G., Santoro, Cristina, Cid, Ana Rosa, Orsini, Sara, Fontana, Pierre, De Candia, Erica, Podda, Gianmarco, Kannan, Meganathan, Jurk, Kerstin, Castaman, Giancarlo, Falaise, Céline, Guglielmini, Giuseppe, Noris, Patrizia, Zaninetti, Carlo, Fiore, Mathieu, Tosetto, Alberto, Zuniga, Pamela, Miyazaki, Koji, Dupuis, Arnaud, Hayward, Catherine, Casonato, Alessandra, Grandone, Elvira, Mazzucconi, Maria Gabriella, James, Paula, Fabris, Fabrizio, Henskens, Yvonne, Napolitano, Mariasanta, Curnow, Jennifer, Gkalea, Vasiliki, Fedor, Marian, Lambert, Michele P., Zieger, Barbara, Barcella, Luca, Cosmi, Benilde, Giordano, Paola, Porri, Claudia, Melazzini, Federica, Abid, Madiha, Glembotsky, Ana C., Ferrara, Grazia, Russo, Alexandra, Deckmyn, Hans, Frelinger, Andrew L., Harrison, Paul, Mezzano, Diego, Mumford, Andrew D, Lordkipanidzé, Marie

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A model-based approach to the automatic diagnosis of von Willebrand disease by Galvanin, Federico, Barolo, Massimiliano, Padrini, Roberto, Casonato, Alessandra, Bezzo, Fabrizio

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