Relationship of white and gray matter abnormalities to clinical and genetic features in myotonic dystrophy type 1

by Zanigni, Stefano, Evangelisti, Stefania, Giannoccaro, Maria Pia, Oppi, Federico, Poda, Roberto, Giorgio, Antonio, Testa, Claudia, Manners, David Neil, Avoni, Patrizia, Gramegna, Laura Ludovica, De Stefano, Nicola, Lodi, Raffaele, Tonon, Caterina, Liguori, Rocco
Published 2016

Syndromic parkinsonism and dementia associated with OPA 1 missense mutations

by Carelli, Valerio, Musumeci, Olimpia, Caporali, Leonardo, Zanna, Claudia, La Morgia, Chiara, Del Dotto, Valentina, Porcelli, Anna Maria, Rugolo, Michela, Valentino, Maria Lucia, Iommarini, Luisa, Maresca, Alessandra, Barboni, Piero, Carbonelli, Michele, Trombetta, Costantino, Valente, Enza Maria, Patergnani, Simone, Giorgi, Carlotta, Pinton, Paolo, Rizzo, Giovanni, Tonon, Caterina, Lodi, Raffaele, Avoni, Patrizia, Liguori, Rocco, Baruzzi, Agostino, Toscano, Antonio, Zeviani, Massimo
Published 2015