FANIN, MARINA
FANIN, MARINA
Autophagy dysregulation in Danon disease
2017 Nascimbeni, ANNA CHIARA; Fanin, Marina; Angelini, Corrado; Sandri, Marco
The role of transmission electron microscopy in vacuole-associated myopathies
2017 Papa, Valentina; Costa, Roberta; D'Angelo, Roberto; Rinaldi, Rita; Pegoraro, Elena; Fanin, Marina; Angelini, Corrado; Cenacchi, Giovanna
Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcript
2016 Todeschini, Alice; Gualandi, Francesca; Trabanelli, Cecilia; Armaroli, Annarita; Ravani, Anna; Fanin, Marina; Rota, Silvia; Bello, Luca; Ferlini, Alessandra; Pegoraro, Elena; Padovani, Alessandro; Filosto, Massimiliano
Functional changes in Becker muscular dystrophy: Implications for clinical trials in dystrophinopathies
2016 Bello, Luca; Campadello, Paola; Barp, Andrea; Fanin, Marina; Semplicini, Claudio; Soraru', Gianni; Caumo, Luca; Calore, Chiara; Angelini, Corrado; Pegoraro, Elena
MYH7-related myopathies: Clinical, histopathological and imaging findings in a cohort of Italian patients
2016 Fiorillo, C.; Astrea, G.; Savarese, M.; Cassandrini, D.; Brisca, G.; Trucco, F.; Pedemonte, M.; Trovato, R.; Ruggiero, L.; Vercelli, L.; D'Amico, A.; Tasca, G.; Pane, M.; Fanin, Marina; Bello, Luca; Broda, P.; Musumeci, O.; Rodolico, C.; Messina, S.; Vita, G. L.; Sframeli, M.; Gibertini, S.; Morandi, L.; Mora, M.; Maggi, L.; Petrucci, A.; Massa, R.; Grandis, M.; Toscano, A.; Pegoraro, Elena; Mercuri, E.; Bertini, E.; Mongini, T.; Santoro, L.; Nigro, V.; Minetti, C.; Santorelli, F. M.; Bruno, C.
The genetic basis of undiagnosed muscular dystrophies and myopathies
2016 Savarese, Marco; Di Fruscio, Giuseppina; Torella, Annalaura; Fiorillo, Chiara; Magri, Francesca; Fanin, Marina; Ruggiero, Lucia; Ricci, Giulia; Astrea, Guja; Passamano, Luigia; Ruggieri, Alessandra; Ronchi, Dario; Tasca, Giorgio; D'Amico, Adele; Janssens, Sandra; Farina, Olimpia; Mutarelli, Margherita; Marwah, Veer Singh; Garofalo, Arcomaria; Giugliano, Teresa; Sanpaolo, Simone; Del Vecchio Blanco, Francesca; Esposito, Gaia; Piluso, Giulio; D'Ambrosio, Paola; Petillo, Roberta; Musumeci, Olimpia; Rodolico, Carmelo; Messina, Sonia; Evilä, Anni; Hackman, Peter; Filosto, Massimiliano; Di Iorio, Giuseppe; Siciliano, Gabriele; Mora, Marina; Maggi, Lorenzo; Minetti, Carlo; Sacconi, Sabrina; Santoro, Lucio; Claes, Kathleen; Vercelli, Liliana; Mongini, Tiziana; Ricci, Enzo; Gualandi, Francesca; Tupler, Rossella; De Bleecker, Jan; Udd, Bjarne; Toscano, Antonio; Moggio, Maurizio; Pegoraro, Elena; Bertini, Enrico; Mercuri, Eugenio; Angelini, Corrado; Santorelli, Filippo Maria; Politano, Luisa; Bruno, Claudio; Comi, Giacomo Pietro; Nigro, Vincenzo
Unveiling the degradative route of the V247M α-sarcoglycan mutant responsible for LGMD-2D.
2014 Bianchini, Elisa; Fanin, Marina; Mamchaoui, K; Betto, R; Sandona', Dorianna
Muscle atrophy in Limb Girdle Muscular Dystrophy 2A: A morphometric and molecular study
2013 Fanin, M.; Nascimbeni, A. C.; Angelini, C.
Muscle atrophy in Limb Girdle Muscular Dystrophy 2A: A morphometric and molecular study
2013 Fanin, M.; Nascimbeni, A. C.; Angelini, C.
TGFB2R but not SPP1 genotype modulates osteopontin expression in Duchenne muscular dystrophy muscle.
2012 Piva, L; Gavassini, Bf; Bello, Luca; Fanin, Marina; Soraru', Gianni; Barp, A; Ermani, Mario; Angelini, C; Hoffman, Ep; Pegoraro, Elena
Comparison of muscle ultrastructure in myasthenia gravis with anti-MuSK and anti-AChR antibodies
2011 Cenacchi, G; Papa, V; Fanin, Marina; Pegoraro, Elena; Angelini, C.
Limb-girdle muscular dystrophy type 1: anticipation or epigenetic modifications?
2011 Angelini, Corrado; Fanin, Marina; Peterle, E.
Study of Muscle Autophagy and Atrophy Markers in Different Phenotypes of Pompe Disease
2011 Nascimbeni, ANNA CHIARA; Fanin, Marina; E., Masiero; Semplicini, Claudio; Tasca, Elisabetta; Sandri, Marco; Angelini, Corrado
Missplicing of Troponin T transcripts in Myotonic dystrophy type 2 human biopsies
2010 Salvatori, Sergio; Picard, ANNE ALEIDA; Furlan, S; Fanin, Marina; Trevisan, CARLO PIETRO; Angelini, Corrado
The role of ultrastructural examination in storage diseases
2010 Papa, V; Tarantino, L; Preda, P; Badiali De Giorgi, L; Fanin, Marina; Pegoraro, Elena; Angelini, Corrado; Cenacchi, G.
Comparative transcriptional and biochemical studies in muscle of myotonic dystrophies (DM1 and DM2)
2009 Salvatori, Sergio; Furlan, S; Fanin, Marina; Picard, ANNE ALEIDA; Pastorello, Ebe; Romeo, Vincenzo; Trevisan, CARLO PIETRO; Angelini, Corrado
Different atrophy-hypertrophy transcription pathways in muscles affected by severe and mild spinal muscular atrophy
2009 Millino, C; Fanin, Marina; Vettori, Andrea; Laveder, Paolo; Mostacciuolo, MARIA LUISA; Angelini, Corrado; Lanfranchi, Gerolamo
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes
2009 Fanin, Marina; Nascimbeni, Ac; Aurino, S; Tasca, Elisabetta; Pegoraro, Elena; Nigro, V; Angelini, Corrado
Muscle histopathology in myasthenia gravis with antibodies against MuSK and AChR
2009 Martignago, S; Fanin, Marina; Albertini, E; Pegoraro, Elena; Angelini, Corrado
Progress in enzyme replacement therapy in glycogen storage disease type II
2009 Angelini, Corrado; Semplicini, Claudio; Tonin, P; Filosto, M; Pegoraro, Elena; Soraru', Gianni; Fanin, Marina