The first reported generation of several induced pluripotent stem cell lines from homozygous and heterozygous Huntington's disease patients demonstrates mutation related enhanced l... von Camnasio, Stefano, Carri, Alessia Delli, Lombardo, Angelo, Grad, Iwona, Mariotti, Caterina, Castucci, Alessia, Rozell, Björn, Riso, Pietro Lo, Castiglioni, Valentina, Zuccato, Chiara, Rochon, Christelle, Takashima, Yasuhiro, Diaferia, Giuseppe, Biunno, Ida, Gellera, Cinzia, Jaconi, Marisa, Smith, Austin, Hovatta, Outi, Naldini, Luigi, Di Donato, Stefano, Feki, Anis, Cattaneo, Elena

Volltext

ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counseling von Gellera, Cinzia, Ticozzi, Nicola, Pensato, Viviana, Nanetti, Lorenzo, Castucci, Alessia, Castellotti, Barbara, Lauria, Giuseppe, Taroni, Franco, Silani, Vincenzo, Mariotti, Caterina

Volltext

Spinocerebellar ataxia type 17 (SCA17) : Oculomotor phenotype and clinical characterization of 15 Italian patients von MARIOTTI, Caterina, ALPINI, Dario, TARONI, Franco, GELLERA, Cinzia, DI DONATO, Stefano, FANCELLU, Roberto, SOLIVERI, Paola, GRISOLI, Marina, RAVAGLIA, Sabrina, LOVATI, Carlo, FETONI, Vincenza, GIACCONE, Giorgio, CASTUCCI, Alessia

Volltext

Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis von Tiloca, Cinzia, Ratti, Antonia, Pensato, Viviana, Castucci, Alessia, Sorarù, Gianni, Del Bo, Roberto, Corrado, Lucia, Cereda, Cristina, D'Ascenzo, Carla, Comi, Giacomo P, Mazzini, Letizia, Castellotti, Barbara, Ticozzi, Nicola, Gellera, Cinzia, Silani, Vincenzo

Volltext