Kif13b Regulates PNS and CNS Myelination through the Dlg1 Scaffold von 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

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JAB1 deletion in oligodendrocytes causes senescence-induced inflammation and neurodegeneration in mice von Rivellini, Cristina, Porrello, Emanuela, Dina, Giorgia, Mrakic-Sposta, Simona, Vezzoli, Alessandra, Bacigaluppi, Marco, Gullotta, Giorgia Serena, Chaabane, Linda, Leocani, Letizia, Marenna, Silvia, Colombo, Emanuela, Farina, Cinthia, Newcombe, Jia, Nave, Klaus-Armin, Pardi, Ruggero, Quattrini, Angelo, Previtali, Stefano C

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Xanthene dyes/amine as photoinitiators of radical polymerization: A comparative and photochemical study in aqueous medium von Encinas, M.V., Rufs, A.M., Bertolotti, S.G., Previtali, C.M.

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Peripheral Nerve Development and the Pathogenesis of Peripheral Neuropathy: the Sorting Point von Previtali, Stefano C.

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Evidentiary basis of the first regulatory qualification of a digital primary efficacy endpoint von Servais, Laurent, Strijbos, Paul, Poleur, Margaux, Mirea, Andrada, Butoianu, Nina, Sansone, Valeria A., Vuillerot, Carole, Schara-Schmidt, Ulrike, Scoto, Mariacristina, Seferian, Andreea M., Previtali, Stefano C., Tulinius, Már, Nascimento, Andrés, Furlong, Pat, Singh, Teji, Dreghici, Roxana Donisa, Goemans, Nathalie, Mercuri, Eugenio, Straub, Volker, Ormazabal, Maitea Guridi, Braid, Jessica, Muntoni, Francesco, Tricot, Alexis, Annoussamy, Mélanie, Eggenspieler, Damien

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Laura Feltri: Of Schwann cells, matrix, and family von Previtali, Stefano C, Taveggia, Carla

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Editorial: Current Insights Into LAMA2 Disease von Previtali, Stefano C., Cohn, Ronald D., Ruegg, Markus A.

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Autocrine and immune cell-derived BDNF in human skeletal muscle: implications for myogenesis and tissue regeneration von Colombo, Emanuela, Bedogni, Francesco, Lorenzetti, Isabella, Landsberger, Nicoletta, Previtali, Stefano C., Farina, Cinthia

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Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle von Boyer, Olivier, Butler-Browne, Gillian, Chinoy, Hector, Cossu, Giulio, Galli, Francesco, Lilleker, James B, Magli, Alessandro, Mouly, Vincent, Perlingeiro, Rita C R, Previtali, Stefano C, Sampaolesi, Maurilio, Smeets, Hubert, Schoewel-Wolf, Verena, Spuler, Simone, Torrente, Yvan, Van Tienen, Florence

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Loss of glial fibrillary acidic protein (GFAP) impairs Schwann cell proliferation and delays nerve regeneration after damage von Triolo, Daniela, Dina, Giorgia, Lorenzetti, Isabella, Malaguti, Mariachiara, Morana, Paolo, Del Carro, Ubaldo, Comi, Giancarlo, Messing, Albee, Quattrini, Angelo, Previtali, Stefano C

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Laura Feltri: In memoriam von Previtali, Stefano C., Taveggia, Carla

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

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Psychosocial resources and psychopathology among persons with neuromuscular disorders during the COVID-19 pandemic von Sanzo', Silvia, Tizzoni, Federica, Previtali, Stefano C, Berardinelli, Angela, Nobile, Maria, Molteni, Massimo, Manzoni, Martina, Tarabelloni, Arianna, Russo, Annamaria, Delle Fave, Antonella, D'Angelo, Maria Grazia

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Phenotypic clustering of lamin A/C mutations in neuromuscular patients von BENEDETTI, S, MENDITTO, I, MORANDI, L, MORONI, I, GALLUZZI, G, BERTINI, E, TOSCANO, A, OLIVE, M, BONNE, G, MARI, F, CALDARA, R, FAZIO, R, DEGANO, M, MAMMI, I, CARRERA, P, TONIOLO, D, COMI, G, QUATTRINI, A, FERRARI, M, PREVITALI, S. C, RODOLICO, C, MERLINI, L, D'AMICO, A, PALMUCCI, L, BERARDINELLI, A, PEGORARO, E, TREVISAN, C. P

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Muscle hypertrophy following acquired neurogenic injury: systematic review and analysis of existing literature von Strano, Camilla MM, Bosco, Luca, Laurini, Christian, Sferruzza, Giacomo, Butera, Carla, Falzone, Yuri M., Sorrenti, Benedetta, Ratti, Adele, Tufano, Laura, Leonardi, Luca, Merlonghi, Gloria, Morino, Stefania, Gerevini, Simonetta, Del Carro, Ubaldo, Garibaldi, Matteo, Filippi, Massimo, Previtali, Stefano C

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Expression of Laminin Receptors in Schwann Cell Differentiation: Evidence for Distinct Roles von Previtali, Stefano C, Nodari, Alessandro, Taveggia, Carla, Pardini, Celia, Dina, Giorgia, Villa, Antonello, Wrabetz, Lawrence, Quattrini, Angelo, Feltri, M. Laura

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Early onset hereditary neuronopathies: an update on non-5q motor neuron diseases von Zambon, Alberto A, Pini, Veronica, Bosco, Luca, Falzone, Yuri M, Munot, Pinki, Muntoni, Francesco, Previtali, Stefano C

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Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4 von 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.

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Motor nerve biopsy: Clinical usefulness and histopathological criteria von Riva, Nilo, Iannaccone, Sandro, Corbo, Massimo, Casellato, Chiara, Sferrazza, Barbara, Lazzerini, Alberto, Scarlato, Marina, Cerri, Federica, Previtali, Stefano C., Nobile-Orazio, Eduardo, Comi, Giancarlo, Quattrini, Angelo

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Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathy von Benedetti, S, Bertini, E, Iannaccone, S, Angelini, C, Trisciani, M, Toniolo, D, Sferrazza, B, Carrera, P, Comi, G, Ferrari, M, Quattrini, A, Previtali, S C

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