Rifino, Nicola http://orcid.org/0000-0002-0423-8759
Bersano, Anna
Padovani, Alessandro
Conti, Giancarlo Maria
Cavallini, Anna
Colombo, Luca
Priori, Alberto
Pianese, Raffaella
Gammone, Maria Rosaria
Erbetta, Alessandra
Ciceri, Elisa Francesca
Sattin, Davide
Varvello, Riccardo
Parati, Eugenio Agostino
Scelzo, Emma
,
Antozzi, Carlo
Pareyson, Davide
Silvani, Antonio
Finocchiaro, Gaetano
Farago’, Giuseppe
Fariselli, Laura
Bruzzone, Maria Grazia
Carriero, Mariarita
Leonardi, Matilde
Mantegazza, Renato
Eleopra, Roberto
DiMeco, Francesco
Ferroli, Paolo
Pollo, Bianca
Mariotti, Caterina
Casali, Cecilia
Pantaleoni, Chiara
Ciano, Claudia
Cazzato, Daniele
Anghileri, Elena
Doniselli, Fabio
Acerbi, Francesco
Giaccone, Giorgio
Zorzi, Giovanna
Vetrano, Ignazio Gaspare
Moroni, Isabella
Brambilla, Laura
Maggi, Lorenzo
Nanetti, Lorenzo
Romito, Luigi Michele
Chiapparini, Luisa
Marchetti, Marcello
Moscatelli, Marco Elvio Manlio
Schiariti, Marco Paolo
Grisoli, Marina
Broggi, Morgan Aldo
Nardocci, Nardo
Lanteri, Paola
Confalonieri, Paolo Agostino
Tiraboschi, Pietro
Morlino, Sara
Esposito, Silvia
D’Arrigo, Stefano
Clerici, Valentina Torri
Cuccarini, Valeria
Zibordi, Federica
Saletti, Veronica
Lucchini, Valeria
Magno, Serena
Persico, Alessandra
Tosi, Piera
Boadu, William
Nava, Stefania
Gipponi, Stefano
Volonghi, Irene
Pezzini, Alessandro
Poli, Loris
Caratozzolo, Salvatore
Cristillo, Viviana
Ranelli, Roberta
Cosseddu, Maura
Turrone, Rosanna
Benazzo, Marco
Del Maestro, Mattia
Luzzi, Sabino
Zoia, Cesare
Sacco, Simona
Ornello, Raffaele
Mariangela, Vanalli
Article History
Received: 18 October 2023
Accepted: 14 November 2023
First Online: 29 November 2023
Declarations
:
: The authors declare no competing interests.
: Informed consent was obtained from all individual participants included in the study.
: The study design will be submitted to the Ethical Committee of the FINCB and of each participating centres for approval. The study will be performed in accordance with the World Medical Association Declaration of Helsinki. Informed written consent for study participation (for data and biological samples collection) from all patients or their legal representatives will be mandatory for study inclusion.