How Schwann Cells Sort Axons: New Concepts

Por Laura, Feltri M., Yannick, Poitelon, Carlo, Previtali Stefano
Publicado no Neuroscientist (2015)

Foot Pad Skin Biopsy in Mouse Models of Hereditary Neuropathy

Por Dacci, Patrizia, Dina, Giorgia, Cerri, Federica, Previtali, Stefano Carlo, Lopez, Ignazio Diego, Lauria, Giuseppe, Feltri, Maria Laura, Bolino, Alessandra, Comi, Giancarlo, Wrabetz, Lawrence, Quattrini, Angelo
Publicado em 2010

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

Por 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
Publicado em 2000

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

Por 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.
Publicado em 2012

Jab1 regulates Schwann cell proliferation and axonal sorting through p27

Por Porrello, Emanuela, Rivellini, Cristina, Dina, Giorgia, Triolo, Daniela, Del Carro, Ubaldo, Ungaro, Daniela, Panattoni, Martina, Feltri, Maria Laura, Wrabetz, Lawrence, Pardi, Ruggero, Quattrini, Angelo, Previtali, Stefano Carlo
Publicado em 2014

Jab1 regulates Schwann cell proliferation and axonal sorting through p27

Por Porrello, Emanuela, Rivellini, Cristina, Dina, Giorgia, Triolo, Daniela, Del Carro, Ubaldo, Ungaro, Daniela, Panattoni, Martina, Feltri, Maria Laura, Wrabetz, Lawrence, Pardi, Ruggero, Quattrini, Angelo, Previtali, Stefano Carlo
Publicado em 2013

Niacin‐mediated Tace activation ameliorates CMT neuropathies with focal hypermyelination

Por Bolino, Alessandra, Piguet, Françoise, Alberizzi, Valeria, Pellegatta, Marta, Rivellini, Cristina, Guerrero‐Valero, Marta, Noseda, Roberta, Brombin, Chiara, Nonis, Alessandro, D'Adamo, Patrizia, Taveggia, Carla, Previtali, Stefano Carlo
Publicado no EMBO Mol Med (2016)

P(0) Glycoprotein Overexpression Causes Congenital Hypomyelination of Peripheral Nerves

Por Wrabetz, Lawrence, Feltri, Maria Laura, Quattrini, Angelo, Imperiale, Daniele, Previtali, Stefano, D'Antonio, Maurizio, Martini, Rudolf, Yin, Xinghua, Trapp, Bruce D., Zhou, Lei, Chiu, Shing-Yan, Messing, Albee
Publicado em 2000

Mesoangioblast delivery of miniagrin ameliorates murine model of merosin-deficient congenital muscular dystrophy type 1A

Por Domi, Teuta, Porrello, Emanuela, Velardo, Daniele, Capotondo, Alessia, Biffi, Alessandra, Tonlorenzi, Rossana, Amadio, Stefano, Ambrosi, Alessandro, Miyagoe-Suzuki, Yuko, Takeda, Shin’ichi, Ruegg, Markus A., Previtali, Stefano Carlo
Publicado no Skelet Muscle (2015)

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

Por 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
Publicado em 2002

ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases

Por Magri, Francesca, Colombo, Irene, Del Bo, Roberto, Previtali, Stefano, Brusa, Roberta, Ciscato, Patrizia, Scarlato, Marina, Ronchi, Dario, D’Angelo, Maria Grazia, Corti, Stefania, Moggio, Maurizio, Bresolin, Nereo, Comi, Giacomo Pietro
Publicado no BMC Neurol (2015)

Disruption of Mtmr2 produces CMT4B1-like neuropathy with myelin outfolding and impaired spermatogenesis

Por Bolino, Alessandra, Bolis, Annalisa, Previtali, Stefano Carlo, Dina, Giorgia, Bussini, Simona, Dati, Gabriele, Amadio, Stefano, Del Carro, Ubaldo, Mruk, Dolores D., Feltri, Maria Laura, Cheng, C. Yan, Quattrini, Angelo, Wrabetz, Lawrence
Publicado em 2004

α6β4 Integrin and Dystroglycan Cooperate to Stabilize the Myelin Sheath

Por 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
Publicado em 2008

Kif13b Regulates PNS and CNS Myelination through the Dlg1 Scaffold

Por 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
Publicado no PLoS Biol (2016)

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

Por 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
Publicado no Eur J Hum Genet (2015)

Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measures

Por Lerario, Alberto, Bonfiglio, Serena, Sormani, MariaPia, Tettamanti, Andrea, Marktel, Sarah, Napolitano, Sara, Previtali, Stefano, Scarlato, Marina, Natali-Sora, MariaGrazia, Mercuri, Eugenio, Bresolin, Nereo, Mongini, Tiziana, Comi, Giancarlo, Gatti, Roberto, Ciceri, Fabio, Cossu, Giulio, Torrente, Yvan
Publicado em 2012

Loss of Fig4 in both Schwann cells and motor neurons contributes to CMT4J neuropathy

Por Vaccari, Ilaria, Carbone, Antonietta, Previtali, Stefano Carlo, Mironova, Yevgeniya A., Alberizzi, Valeria, Noseda, Roberta, Rivellini, Cristina, Bianchi, Francesca, Del Carro, Ubaldo, D'Antonio, Maurizio, Lenk, Guy M., Wrabetz, Lawrence, Giger, Roman J., Meisler, Miriam H., Bolino, Alessandra
Publicado no Hum Mol Genet (2015)

Longitudinal MRI quantification of muscle degeneration in Duchenne muscular dystrophy

Por 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.
Publicado no Ann Clin Transl Neurol (2016)

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

Por 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
Publicado no EMBO Mol Med (2015)

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

Por 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
Publicado em 2012