Optic atrophy plus phenotype due to mutations in the OPA1 gene: Two more Italian families

por Ranieri, Michela, Del Bo, Roberto, Bordoni, Andreina, Ronchi, Dario, Colombo, Irene, Riboldi, Giulietta, Cosi, Alessandra, Servida, Maura, Magri, Francesca, Moggio, Maurizio, Bresolin, Nereo, Comi, Giacomo P., Corti, Stefania
Publicado 2012

Survival gain in glioblastoma patients treated with dendritic cell immunotherapy is associated with increased NK but not CD8(+) T cell activation in the presence of adjuvant temozo...

por Pellegatta, Serena, Eoli, Marica, Cuccarini, Valeria, Anghileri, Elena, Pollo, Bianca, Pessina, Sara, Frigerio, Simona, Servida, Maura, Cuppini, Lucia, Antozzi, Carlo, Cuzzubbo, Stefania, Corbetta, Cristina, Paterra, Rosina, Acerbi, Francesco, Ferroli, Paolo, DiMeco, Francesco, Fariselli, Laura, Parati, Eugenio A., Bruzzone, Maria Grazia, Finocchiaro, Gaetano
Publicado 2018

Large scale genotype–phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy

por Ricci, Giulia, Scionti, Isabella, Sera, Francesco, Govi, Monica, D’Amico, Roberto, Frambolli, Ilaria, Mele, Fabiano, Filosto, Massimiliano, Vercelli, Liliana, Ruggiero, Lucia, Berardinelli, Angela, Angelini, Corrado, Antonini, Giovanni, Bucci, Elisabetta, Cao, Michelangelo, Daolio, Jessica, Di Muzio, Antonio, Di Leo, Rita, Galluzzi, Giuliana, Iannaccone, Elisabetta, Maggi, Lorenzo, Maruotti, Valerio, Moggio, Maurizio, Mongini, Tiziana, Morandi, Lucia, Nikolic, Ana, Pastorello, Ebe, Ricci, Enzo, Rodolico, Carmelo, Santoro, Lucio, Servida, Maura, Siciliano, Gabriele, Tomelleri, Giuliano, Tupler, Rossella
Publicado 2013