Noncoding RNAs in Duchenne and Becker muscular dystrophies: role in pathogenesis and future prognostic and therapeutic perspectives von Brusa, Roberta, Magri, Francesca, Bresolin, Nereo, Comi, Giacomo Pietro, Corti, Stefania

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Therapeutic Development in Amyotrophic Lateral Sclerosis von Bucchia, Monica, MS, Ramirez, Agnese, MS, Parente, Valeria, PhD, Simone, Chiara, PhD, Nizzardo, Monica, PhD, Magri, Francesca, MD, Dametti, Sara, MS, Corti, Stefania, MD, PhD

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SOD1 misplacing and mitochondrial dysfunction in amyotrophic lateral sclerosis pathogenesis von Tafuri, Francesco, Ronchi, Dario, Magri, Francesca, Comi, Giacomo P, Corti, Stefania

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Recurrence of alopecia areata after covid‐19 vaccination: A report of three cases in Italy von Rossi, Alfredo, Magri, Francesca, Michelini, Simone, Caro, Gemma, Di Fraia, Marco, Fortuna, Maria Caterina, Pellacani, Giovanni, Carlesimo, Marta

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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, 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

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Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patients von Faravelli, Irene, Meneri, Megi, Saccomanno, Domenica, Velardo, Daniele, Abati, Elena, Gagliardi, Delia, Parente, Valeria, Petrozzi, Lucia, Ronchi, Dario, Stocchetti, Nino, Calderini, Edoardo, D’Angelo, Grazia, Chidini, Giovanna, Prandi, Edi, Ricci, Giulia, Siciliano, Gabriele, Bresolin, Nereo, Comi, Giacomo Pietro, Corti, Stefania, Magri, Francesca, Govoni, Alessandra

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Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies von Piga, Daniela, Salani, Sabrina, Magri, Francesca, Brusa, Roberta, Mauri, Eleonora, Comi, Giacomo P., Bresolin, Nereo, Corti, Stefania

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Concomitant segmental vitiligo and segmental morphea in an 8-year-old boy von Magri, Francesca, Miraglia, Emanuele, Soda, Giuseppe, Giustini, Sandra

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Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophy von Govoni, Alessandra, Magri, Francesca, Brajkovic, Simona, Zanetta, Chiara, Faravelli, Irene, Corti, Stefania, Bresolin, Nereo, Comi, Giacomo P

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Mutations in DNA2 Link Progressive Myopathy to Mitochondrial DNA Instability von Ronchi, Dario, Di Fonzo, Alessio, Lin, Weiqiang, Bordoni, Andreina, Liu, Changwei, Fassone, Elisa, Pagliarani, Serena, Rizzuti, Mafalda, Zheng, Li, Filosto, Massimiliano, Ferrò, Maria Teresa, Ranieri, Michela, Magri, Francesca, Peverelli, Lorenzo, Li, Hongzhi, Yuan, Yate-Ching, Corti, Stefania, Sciacco, Monica, Moggio, Maurizio, Bresolin, Nereo, Shen, Binghui, Comi, Giacomo Pietro

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Genetic Modifiers of Duchenne Muscular Dystrophy and Dilated Cardiomyopathy von Barp, Andrea, Bello, Luca, Politano, Luisa, Melacini, Paola, Calore, Chiara, Polo, Angela, Vianello, Sara, Sorarù, Gianni, Semplicini, Claudio, Pantic, Boris, Taglia, Antonella, Picillo, Ester, Magri, Francesca, Gorni, Ksenija, Messina, Sonia, Vita, Gian Luca, Vita, Giuseppe, Comi, Giacomo P, Ermani, Mario, Calvo, Vincenzo, Angelini, Corrado, Hoffman, Eric P, Pegoraro, Elena

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6 Minute walk test in Duchenne MD patients with different mutations: 12 month changes von Pane, Marika, Mazzone, Elena S, Sormani, Maria Pia, Messina, Sonia, Vita, Gian Luca, Fanelli, Lavinia, Berardinelli, Angela, Torrente, Yvan, D'Amico, Adele, Lanzillotta, Valentina, Viggiano, Emanuela, D'Ambrosio, Paola, Cavallaro, Filippo, Frosini, Silvia, Bello, Luca, Bonfiglio, Serena, Scalise, Roberta, De Sanctis, Roberto, Rolle, Enrica, Bianco, Flaviana, Van der Haawue, Marlene, Magri, Francesca, Palermo, Concetta, Rossi, Francesca, Donati, Maria Alice, Alfonsi, Chiara, Sacchini, Michele, Arnoldi, Maria Teresa, Baranello, Giovanni, Mongini, Tiziana, Pini, Antonella, Battini, Roberta, Pegoraro, Elena, Previtali, Stefano C, Napolitano, Sara, Bruno, Claudio, Politano, Luisa, Comi, Giacomo P, Bertini, Enrico, Morandi, Lucia, Gualandi, Francesca, Ferlini, Alessandra, Goemans, Nathalie, Mercuri, Eugenio

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Muscle histological changes in a large cohort of patients affected with Becker muscular dystrophy von Ripolone, Michela, Velardo, Daniele, Mondello, Stefania, Zanotti, Simona, Magri, Francesca, Minuti, Elisa, Cazzaniga, Sara, Fortunato, Francesco, Ciscato, Patrizia, Tiberio, Francesca, Sciacco, Monica, Moggio, Maurizio, Bettica, Paolo, Comi, Giacomo P

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Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions von Johari, Mridul, Sarparanta, Jaakko, Vihola, Anna, Jonson, Per Harald, Savarese, Marco, Jokela, Manu, Torella, Annalaura, Piluso, Giulio, Said, Edith, Vella, Norbert, Cauchi, Marija, Magot, Armelle, Magri, Francesca, Mauri, Eleonora, Kornblum, Cornelia, Reimann, Jens, Stojkovic, Tanya, Romero, Norma B., Luque, Helena, Huovinen, Sanna, Lahermo, Päivi, Donner, Kati, Comi, Giacomo Pietro, Nigro, Vincenzo, Hackman, Peter, Udd, Bjarne

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Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant von Rimoldi, Martina, Magri, Francesca, Antognozzi, Sara, Ripolone, Michela, Salani, Sabrina, Piga, Daniela, Bertolasi, Letizia, Zanotti, Simona, Ciscato, Patrizia, Fortunato, Francesco, Moggio, Maurizio, Corti, Stefania, Comi, Giacomo Pietro, Ronchi, Dario

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24 month longitudinal data in ambulant boys with Duchenne muscular dystrophy von Mazzone, Elena Stacy, Pane, Marika, Sormani, Maria Pia, Scalise, Roberta, Berardinelli, Angela, Messina, Sonia, Torrente, Yvan, D'Amico, Adele, Doglio, Luca, Viggiano, Emanuela, D'Ambrosio, Paola, Cavallaro, Filippo, Frosini, Silvia, Bello, Luca, Bonfiglio, Serena, De Sanctis, Roberto, Rolle, Enrica, Bianco, Flaviana, Magri, Francesca, Rossi, Francesca, Vasco, Gessica, Vita, Gianluca, Motta, Maria Chiara, Donati, Maria Alice, Sacchini, Michele, Mongini, Tiziana, Pini, Antonella, Battini, Roberta, Pegoraro, Elena, Previtali, Stefano, Napolitano, Sara, Bruno, Claudio, Politano, Luisa, Comi, Giacomo Pietro, Bertini, Enrico, Mercuri, Eugenio

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

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Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutation von Scarcella, Simone, Dell'Arti, Laura, Gagliardi, Delia, Magri, Francesca, Govoni, Alessandra, Velardo, Daniele, Mainetti, Claudia, Minorini, Valeria, Ronchi, Dario, Piga, Daniela, Comi, Giacomo Pietro, Corti, Stefania, Meneri, Megi

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Case report: A novel ACTA1 variant in a patient with nemaline rods and increased glycogen deposition von Piga, Daniela, Rimoldi, Martina, Magri, Francesca, Zanotti, Simona, Napoli, Laura, Ripolone, Michela, Pagliarani, Serena, Ciscato, Patrizia, Velardo, Daniele, D'Amico, Adele, Bertini, Enrico, Comi, Giacomo Pietro, Ronchi, Dario, Corti, Stefania

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Immunofluorescence signal intensity measurements as a semi-quantitative tool to assess sarcoglycan complex expression in muscle biopsy von Zanotti, Simona, Magri, Francesca, Poggetti, Francesca, Ripolone, Michela, Velardo, Daniele, Fortunato, Francesco, Ciscato, Patrizia, Moggio, Maurizio, Corti, Stefania, Comi, Giacomo Pietro, Sciacco, Monica

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