Brain connectivity abnormalities extend beyond the sensorimotor network in peripheral neuropathy

by Rocca, Maria A., Valsasina, Paola, Fazio, Raffaella, Previtali, Stefano C., Messina, Roberta, Falini, Andrea, Comi, Giancarlo, Filippi, Massimo
Published in Hum Brain Mapp (2012)

Expression of Laminin Receptors in Schwann Cell Differentiation: Evidence for Distinct Roles

by Previtali, Stefano C., Nodari, Alessandro, Taveggia, Carla, Pardini, Celia, Dina, Giorgia, Villa, Antonello, Wrabetz, Lawrence, Quattrini, Angelo, Feltri, M. Laura
Published in J Neurosci (2003)

Alteration of the late endocytic pathway in Charcot–Marie–Tooth type 2B disease

by Romano, Roberta, Rivellini, Cristina, De Luca, Maria, Tonlorenzi, Rossana, Beli, Raffaella, Manganelli, Fiore, Nolano, Maria, Santoro, Lucio, Eskelinen, Eeva-Liisa, Previtali, Stefano C., Bucci, Cecilia
Published in Cell Mol Life Sci (2020)

Epitope-Tagged P(0)Glycoprotein Causes Charcot-Marie-Tooth–Like Neuropathy in Transgenic Mice

by Previtali, Stefano C., Quattrini, Angelo, Fasolini, Marina, Panzeri, Maria Carla, Villa, Antonello, Filbin, Marie T., Li, Wenhui, Chiu, Shing-Yan, Messing, Albee, Wrabetz, Lawrence, Feltri, M. Laura
Published 2000

Urokinase Plasminogen Receptor and the Fibrinolytic Complex Play a Role in Nerve Repair after Nerve Crush in Mice, and in Human Neuropathies

by Rivellini, Cristina, Dina, Giorgia, Porrello, Emanuela, Cerri, Federica, Scarlato, Marina, Domi, Teuta, Ungaro, Daniela, Carro, Ubaldo Del, Bolino, Alessandra, Quattrini, Angelo, Comi, Giancarlo, Previtali, Stefano C.
Published 2012

Conditional disruption of β1 integrin in Schwann cells impedes interactions with axons

by Feltri, M. Laura, Porta, Diana Graus, Previtali, Stefano C., Nodari, Alessandro, Migliavacca, Barbara, Cassetti, Arianna, Littlewood-Evans, Amanda, Reichardt, Louis F., Messing, Albee, Quattrini, Angelo, Mueller, Ulrich, Wrabetz, Lawrence
Published 2002

Sodium Channel Myotonia Due to Novel Mutations in Domain I of Na(v)1.4

by Pagliarani, Serena, Lucchiari, Sabrina, Scarlato, Marina, Redaelli, Elisa, Modoni, Anna, Magri, Francesca, Fossati, Barbara, Previtali, Stefano C., Sansone, Valeria A., Lecchi, Marzia, Lo Monaco, Mauro, Meola, Giovanni, Comi, Giacomo P.
Published in Front Neurol (2020)

α6β4 Integrin and Dystroglycan Cooperate to Stabilize the Myelin Sheath

by Nodari, Alessandro, Previtali, Stefano C., Dati, Gabriele, Occhi, Simona, Court, Felipe A., Colombelli, Cristina, Zambroni, Desirée, Dina, Giorgia, Del Carro, Ubaldo, Campbell, Kevin P., Quattrini, Angelo, Wrabetz, Lawrence, Feltri, M. Laura
Published 2008

Kif13b Regulates PNS and CNS Myelination through the Dlg1 Scaffold

by Noseda, Roberta, Guerrero-Valero, Marta, Alberizzi, Valeria, Previtali, Stefano C., Sherman, Diane L., Palmisano, Marilena, Huganir, Richard L., Nave, Klaus-Armin, Cuenda, Ana, Feltri, Maria Laura, Brophy, Peter J., Bolino, Alessandra
Published in PLoS Biol (2016)

The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy

by Robusto, Michela, Fang, Mingyan, Asselta, Rosanna, Castorina, Pierangela, Previtali, Stefano C, Caccia, Sonia, Benzoni, Elena, De Cristofaro, Raimondo, Yu, Cong, Cesarani, Antonio, Liu, Xuanzhu, Li, Wangsheng, Primignani, Paola, Ambrosetti, Umberto, Xu, Xun, Duga, Stefano, Soldà, Giulia
Published in Eur J Hum Genet (2015)

Rimeporide as a first- in-class NHE-1 inhibitor: Results of a phase Ib trial in young patients with Duchenne Muscular Dystrophy

by Previtali, Stefano C., Gidaro, Teresa, Díaz-Manera, Jordi, Zambon, Alberto, Carnesecchi, Stephanie, Roux-Lombard, Pascale, Spitali, Pietro, Signorelli, Mirko, Szigyarto, Cristina Al-Khalili, Johansson, Camilla, Gray, Julian, Labolle, Delphine, Porte Thomé, Florence, Pitchforth, Jacqueline, Domingos, Joana, Muntoni, Francesco
Published in Pharmacol Res (2020)

Longitudinal MRI quantification of muscle degeneration in Duchenne muscular dystrophy

by Godi, Claudia, Ambrosi, Alessandro, Nicastro, Francesca, Previtali, Stefano C., Santarosa, Corrado, Napolitano, Sara, Iadanza, Antonella, Scarlato, Marina, Natali Sora, Maria Grazia, Tettamanti, Andrea, Gerevini, Simonetta, Cicalese, Maria Pia, Sitzia, Clementina, Venturini, Massimo, Falini, Andrea, Gatti, Roberto, Ciceri, Fabio, Cossu, Giulio, Torrente, Yvan, Politi, Letterio S.
Published in Ann Clin Transl Neurol (2016)

Pregnancy in Charcot-Marie-Tooth disease: Data from the Italian CMT national registry

by Pisciotta, Chiara, Calabrese, Daniela, Santoro, Lucio, Tramacere, Irene, Manganelli, Fiore, Fabrizi, Gian Maria, Schenone, Angelo, Cavallaro, Tiziana, Grandis, Marina, Previtali, Stefano C., Allegri, Isabella, Padua, Luca, Pazzaglia, Costanza, Saveri, Paola, Quattrone, Aldo, Valentino, Paola, Tozza, Stefano, Gentile, Luca, Russo, Massimo, Mazzeo, Anna, Trapasso, Maria Claudia, Parazzini, Fabio, Vita, Giuseppe, Pareyson, Davide
Published in Neurology (2020)

Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53

by Brogna, Claudia, Coratti, Giorgia, Pane, Marika, Ricotti, Valeria, Messina, Sonia, D’Amico, Adele, Bruno, Claudio, Vita, Gianluca, Berardinelli, Angela, Mazzone, Elena, Magri, Francesca, Ricci, Federica, Mongini, Tiziana, Battini, Roberta, Bello, Luca, Pegoraro, Elena, Baranello, Giovanni, Previtali, Stefano C., Politano, Luisa, Comi, Giacomo P., Sansone, Valeria A., Donati, Alice, Bertini, Enrico, Muntoni, Francesco, Goemans, Nathalie, Mercuri, Eugenio
Published in PLoS One (2019)

Correction: Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53

by Brogna, Claudia, Coratt, Giorgia, Pane, Marika, Ricotti, Valeria, Messina, Sonia, D’Amico, Adele, Bruno, Claudio, Vita, Gianluca, Berardinelli, Angela, Mazzone, Elena, Magri, Francesca, Ricci, Federica, Mongini, Tiziana, Battini, Roberta, Bello, Luca, Pegoraro, Elena, Baranello, Giovanni, Previtali, Stefano C., Politano, Luisa, Comi, Giacomo P., Sansone, Valeria A., Donati, Alice, Bertini, Enrico, Muntoni, Francesco, Goemans, Nathalie, Mercuri, Eugenio
Published in PLoS One (2019)

Large genotype–phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis

by Ricci, Giulia, Mele, Fabiano, Govi, Monica, Ruggiero, Lucia, Sera, Francesco, Vercelli, Liliana, Bettio, Cinzia, Santoro, Lucio, Mongini, Tiziana, Villa, Luisa, Moggio, Maurizio, Filosto, Massimiliano, Scarlato, Marina, Previtali, Stefano C., Tripodi, Silvia Maria, Pegoraro, Elena, Telese, Roberta, Di Muzio, Antonio, Rodolico, Carmelo, Bucci, Elisabetta, Antonini, Giovanni, D’Angelo, Maria Grazia, Berardinelli, Angela, Maggi, Lorenzo, Piras, Rachele, Maioli, Maria Antonietta, Siciliano, Gabriele, Tomelleri, Giuliano, Angelini, Corrado, Tupler, Rossella
Published in Sci Rep (2020)

Intra‐arterial transplantation of HLA‐matched donor mesoangioblasts in Duchenne muscular dystrophy

by Cossu, Giulio, Previtali, Stefano C, Napolitano, Sara, Cicalese, Maria Pia, Tedesco, Francesco Saverio, Nicastro, Francesca, Noviello, Maddalena, Roostalu, Urmas, Natali Sora, Maria Grazia, Scarlato, Marina, De Pellegrin, Maurizio, Godi, Claudia, Giuliani, Serena, Ciotti, Francesca, Tonlorenzi, Rossana, Lorenzetti, Isabella, Rivellini, Cristina, Benedetti, Sara, Gatti, Roberto, Marktel, Sarah, Mazzi, Benedetta, Tettamanti, Andrea, Ragazzi, Martina, Imro, Maria Adele, Marano, Giuseppina, Ambrosi, Alessandro, Fiori, Rossana, Sormani, Maria Pia, Bonini, Chiara, Venturini, Massimo, Politi, Letterio S, Torrente, Yvan, Ciceri, Fabio
Published in EMBO Mol Med (2015)

Intra‐arterial transplantation of HLA‐matched donor mesoangioblasts in Duchenne muscular dystrophy

by Cossu, Giulio, Previtali, Stefano C, Napolitano, Sara, Cicalese, Maria Pia, Tedesco, Francesco Saverio, Nicastro, Francesca, Noviello, Maddalena, Roostalu, Urmas, Natali Sora, Maria Grazia, Scarlato, Marina, De Pellegrin, Maurizio, Godi, Claudia, Giuliani, Serena, Ciotti, Francesca, Tonlorenzi, Rossana, Lorenzetti, Isabella, Rivellini, Cristina, Benedetti, Sara, Gatti, Roberto, Marktel, Sarah, Mazzi, Benedetta, Tettamanti, Andrea, Ragazzi, Martina, Imro, Maria Adele, Marano, Giuseppina, Ambrosi, Alessandro, Fiori, Rossana, Sormani, Maria Pia, Bonini, Chiara, Venturini, Massimo, Politi, Letterio S, Torrente, Yvan, Ciceri, Fabio
Published in EMBO Mol Med (2016)

North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up

by Coratti, Giorgia, Pane, Marika, Brogna, Claudia, Ricotti, Valeria, Messina, Sonia, D’Amico, Adele, Bruno, Claudio, Vita, Gianluca, Berardinelli, Angela, Mazzone, Elena, Magri, Francesca, Ricci, Federica, Mongini, Tiziana, Battini, Roberta, Bello, Luca, Pegoraro, Elena, Baranello, Giovanni, Previtali, Stefano C., Politano, Luisa, Comi, Giacomo P., Sansone, Valeria A., Donati, Alice, Hogrel, Jean Yves, Straub, Volker, De Lucia, Silvana, Niks, Erik, Servais, Laurent, De Groot, Imelda, Chesshyre, Mary, Bertini, Enrico, Goemans, Nathalie, Muntoni, Francesco, Mercuri, Eugenio
Published in PLoS One (2021)

Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy

by Bello, Luca, Piva, Luisa, Barp, Andrea, Taglia, Antonella, Picillo, Esther, Vasco, Gessica, Pane, Marika, Previtali, Stefano C., Torrente, Yvan, Gazzerro, Elisabetta, Chiara Motta, Maria, Grieco, Gaetano S., Napolitano, Sara, Magri, Francesca, D'Amico, Adele, Astrea, Guja, Messina, Sonia, Sframeli, Maria, Luca Vita, Gian, Boffi, Patrizia, Mongini, Tiziana, Ferlini, Alessandra, Gualandi, Francesca, Soraru', Gianni, Ermani, Mario, Vita, Giuseppe, Battini, Roberta, Bertini, Enrico, Comi, Giacomo P., Berardinelli, Angela, Minetti, Carlo, Bruno, Claudio, Mercuri, Eugenio, Politano, Luisa, Angelini, Corrado, Hoffman, Eric P., Pegoraro, Elena
Published 2012