PREVITALI, STEFANO CARLO
PREVITALI, STEFANO CARLO
Facoltà di Medicina e Chirurgia
24 Month Longitudinal Data in Ambulant Boys with Duchenne Muscular Dystrophy
2013-01-01 Mazzone, Es; Pane, M; Sormani, Mp; Scalise, R; Berardinelli, A; Messina, S; Torrente, Y; D'Amico, A; Doglio, L; Viggiano, E; D'Ambrosio, P; Cavallaro, F; Frosini, S; Bello, L; Bonfiglio, S; De Sanctis, R; Rolle, E; Bianco, F; Magri, F; Rossi, F; Vasco, G; Vita, G; Motta, Mc; Donati, Ma; Sacchini, M; Mongini, T; Pini, A; Battini, R; Pegoraro, E; Previtali, S; Napolitano, S; Bruno, C; Politano, L; Comi, Gp; Bertini, E; Mercuri, E.
6 Minute Walk Test in Duchenne MD Patients with Different Mutations: 12 Month Changes
2014-01-01 Pane, M; Mazzone, Es; Sormani, Mp; Messina, S; Vita, Gl; Fanelli, L; Berardinelli, A; Torrente, Y; D'Amico, A; Lanzillotta, V; Viggiano, E; D'Ambrosio, P; Cavallaro, F; Frosini, S; Bello, L; Bonfiglio, S; Scalise, R; De Sanctis, R; Rolle, E; Bianco, F; Van der Haawue, M; Magri, F; Palermo, C; Rossi, F; Donati, Ma; Alfonsi, C; Sacchini, M; Arnoldi, Mt; Baranello, G; Mongini, T; Pini, A; Battini, R; Pegoraro, E; Previtali, S; Napolitano, S; Bruno, C; Politano, L; Comi, Gp; Bertini, E; Morandi, L; Gualandi, F; Ferlini, A; Goemans, N; Mercuri, E.
A 5-year clinical follow-up study from the Italian National Registry for FSHD
2021-01-01 Vercelli, L; Mele, F; Ruggiero, L; Sera, F; Tripodi, S; Ricci, G; Vallarola, A; Villa, L; Govi, M; Maranda, L; Di Muzio, A; Scarlato, M; Bucci, E; Maggi, L; Rodolico, C; Moggio, M; Filosto, M; Antonini, G; Previtali, S; Angelini, C; Berardinelli, A; Pegoraro, E; Siciliano, G; Tomelleri, G; Santoro, L; Mongini, T; Tupler, R
A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs)
2019-01-01 Pareyson, D.; Stojkovic, T.; Reilly, M. M.; Leonard-Louis, S.; Laura, M.; Blake, J.; Parman, Y.; Battaloglu, E.; Tazir, M.; Bellatache, M.; Bonello-Palot, N.; Levy, N.; Sacconi, S.; Guimaraes-Costa, R.; Attarian, S.; Latour, P.; Sole, G.; Megarbane, A.; Horvath, R.; Ricci, G.; Choi, B. -O.; Schenone, A.; Gemelli, C.; Geroldi, A.; Sabatelli, M.; Luigetti, M.; Santoro, L.; Manganelli, F.; Quattrone, A.; Valentino, P.; Murakami, T.; Scherer, S. S.; Dankwa, L.; Shy, M. E.; Bacon, C. J.; Herrmann, D. N.; Zambon, A.; Tramacere, I.; Pisciotta, C.; Magri, S.; Previtali, S. C.; Bolino, A.
A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation.
2015-01-01 Scarlato, M; Nuara, A; Gerevini, S; Benedetti, S; P., Rossi; Ferrari, Maurizio; Previtali, S. C.
A novel heat shock protein 27 homozygous mutation: widening of the continuum between MND/dHMN/CMT2
2015-01-01 Scarlato, M; Vigano, F; Carrera, P; Previtali, Sc; Bolino, A
A whole-brain network analysis in patients with hereditary and acquired peripheral neuropathy
2012-01-01 Rocca, Ma; Valsasina, P; Fazio, R; Previtali, S; Falini, A; Comi, G; Filippi, M
Alteration of the late endocytic pathway in Charcot-Marie-Tooth type 2B disease
2020-01-01 Romano, R; Rivellini, C; De Luca, M; Tonlorenzi, R; Beli, R; Manganelli, F; Nolano, M; Santoro, L; Eskelinen, El; Previtali, S; Bucci, C
Analyzing histopathological features of rare charcot-marie-tooth neuropathies to unravel their pathogenesis
2010-01-01 Benedetti, S; Previtali, Sc; Coviello, S; Scarlato, M; Cerri, F; DI PIERRI, E; Piantoni, L; Spiga, I; Fazio, R; Riva, N; NATALI SORA, Mg; Dacci, P; Malaguti, Mc; Munerati, E; Grimaldi, Lm; Marrosu, Mg; DE PELLEGRIN, M; Ferrari, Maurizio; Comi, Giancarlo; Quattrini, A; Bolino, A.
Animal Models as a Tool to Design Therapeutical Strategies for CMT-like Hereditary Neuropathies
2021-01-01 Bosco, L; Falzone, Ym; Previtali, S
Autocrine and immune cell-derived BDNF in human skeletal muscle: implications for myogenesis and tissue regeneration
2013-01-01 Colombo, E; Bedogni, F; Lorenzetti, I; Landsberger, N; Previtali, S; Farina, C.
Begelomab for severe refractory dermatomyositis: A case report
2021-01-01 De Lorenzo, R.; Sciorati, C.; Monno, A.; Cavalli, S.; Bonomi, F.; Tronci, S.; Previtali, S.; Rovere-Querini, P.
Brain connectivity abnormalities extend beyond the sensorimotor network in peripheral neuropathy
2014-01-01 Rocca, Ma; Valsasina, P; Fazio, R; Previtali, Sc; Messina, R; Falini, Andrea; Comi, Giancarlo; Filippi, Massimo
Cardiac and Neuromuscular Features of Patients with LMNA-Related Cardiomyopathy
2019-01-01 Peretto, Giovanni; Di Resta, Chiara; Perversi, Jacopo; Forleo, Cinzia; Maggi, Lorenzo; Politano, Luisa; Barison, Andrea; Previtali, Stefano C; Carboni, Nicola; Brun, Francesca; Pegoraro, Elena; D'Amico, Adele; Rodolico, Carmelo; Magri, Francesca; Manzi, Rosa C; Palladino, Alberto; Isola, Franco; Gigli, Lorenzo; Mongini, Tiziana E; Semplicini, Claudio; Calore, Chiara; Ricci, Giulia; Comi, Giacomo P; Ruggiero, Lucia; Bertini, Enrico; Bonomo, Paolo; Nigro, Gerardo; Resta, Nicoletta; Emdin, Michele; Favale, Stefano; Siciliano, Gabriele; Santoro, Lucio; Sinagra, Gianfranco; Limongelli, Giuseppe; Ambrosi, Alessandro; Ferrari, Maurizio; Golzio, Pier G; Bella, Paolo Della; Benedetti, Sara; Sala, Simone
Categorizing natural history trajectories of ambulatory function measured by the 6-minute walk distance in patients with Duchenne muscular dystrophy
2016-01-01 Mercuri, E; Signorovitch, Je; Swallow, E; Song, J; Ward, Sj; Pane, M1; Mazzone, E; Messina, S; Vita, Gl; Sormani, Mp; D'Amico, A; Berardinelli, A; Magri, F; Comi, Gp; Baranello, G; Mongini, T; Pini, A; Battini, R; Pegoraro, E; Bruno, C; Politano, L; Previtali, S; Binks, Mh; Campion, G; Charnas, L; Kaye, E; Kelly, M; Morris, C; Reha, A; Trajectory Analysis Project, (cTAP)
Charcot-Marie-Tooth type 4B demyelinating neuropathy: deciphering the role of MTMR phosphatases
2007-01-01 Previtali, S; Quattrini, A; Bolino, A
CSN5/JAB1 PLAYS A ROLE IN AXONAL SORTING AND MYELINATION IN PERIPHERAL NERVE
2012-01-01 Porrello, E; Rivellini, C; Dina, G; Triolo, D; Pardi, R; Wrabetz, L; Feltri, Ml; Quattrini, A; Previtali, S
CSN5/JAB1 REGULATES SCHWANN CELL-AXON INTERACTION AND PLAYS A ROLE IN PERIPHERAL NERVE DEVELOPMENT AND FUNCTION
2009-01-01 Porrello, E; Cerri, F; Dina, G; Triolo, D; Lopez, Id; Panattoni, M; Del Carro, U; Morana, P; Comi, G; Wrabetz, L; Feltri, Ml; Pardi, R; Quattrini, A; Previtali, S
DEFINING GENOTYPE-PHENOTYPE CORRELATIONS IN THE CMT NEUROPATHIES
2009-01-01 Benedetti, S; Coviello, S; Colombo, A; Piantoni, L; Spiga, I; Cerri, F; Scarlato, M; Fazio, R; Quattrini, A; Previtali, Sc; Bolino, A
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements
2017-01-01 D'Amico, A; Catteruccia, M; Baranello, G; Politano, L; Govoni, A; Previtali, S; Pane, M; D'Angelo, Mg; Bruno, C; Messina, S; Ricci, F; Pegoraro, E; Pini, A; Berardinelli, A; Gorni, K; Battini, R; Vita, G; Trucco, F; Scutifero, M; Petillo, R; D'Ambrosio, P; Ardissone, A; Pasanisi, B; Vita, G; Mongini, T; Moggio, M; Comi, Gp; Mercuri, E; Bertini, E
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 24 Month Longitudinal Data in Ambulant Boys with Duchenne Muscular Dystrophy | 1-gen-2013 | Mazzone, Es; Pane, M; Sormani, Mp; Scalise, R; Berardinelli, A; Messina, S; Torrente, Y; D'Amico, A; Doglio, L; Viggiano, E; D'Ambrosio, P; Cavallaro, F; Frosini, S; Bello, L; Bonfiglio, S; De Sanctis, R; Rolle, E; Bianco, F; Magri, F; Rossi, F; Vasco, G; Vita, G; Motta, Mc; Donati, Ma; Sacchini, M; Mongini, T; Pini, A; Battini, R; Pegoraro, E; Previtali, S; Napolitano, S; Bruno, C; Politano, L; Comi, Gp; Bertini, E; Mercuri, E. | |
| 6 Minute Walk Test in Duchenne MD Patients with Different Mutations: 12 Month Changes | 1-gen-2014 | Pane, M; Mazzone, Es; Sormani, Mp; Messina, S; Vita, Gl; Fanelli, L; Berardinelli, A; Torrente, Y; D'Amico, A; Lanzillotta, V; Viggiano, E; D'Ambrosio, P; Cavallaro, F; Frosini, S; Bello, L; Bonfiglio, S; Scalise, R; De Sanctis, R; Rolle, E; Bianco, F; Van der Haawue, M; Magri, F; Palermo, C; Rossi, F; Donati, Ma; Alfonsi, C; Sacchini, M; Arnoldi, Mt; Baranello, G; Mongini, T; Pini, A; Battini, R; Pegoraro, E; Previtali, S; Napolitano, S; Bruno, C; Politano, L; Comi, Gp; Bertini, E; Morandi, L; Gualandi, F; Ferlini, A; Goemans, N; Mercuri, E. | |
| A 5-year clinical follow-up study from the Italian National Registry for FSHD | 1-gen-2021 | Vercelli, L; Mele, F; Ruggiero, L; Sera, F; Tripodi, S; Ricci, G; Vallarola, A; Villa, L; Govi, M; Maranda, L; Di Muzio, A; Scarlato, M; Bucci, E; Maggi, L; Rodolico, C; Moggio, M; Filosto, M; Antonini, G; Previtali, S; Angelini, C; Berardinelli, A; Pegoraro, E; Siciliano, G; Tomelleri, G; Santoro, L; Mongini, T; Tupler, R | |
| A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs) | 1-gen-2019 | Pareyson, D.; Stojkovic, T.; Reilly, M. M.; Leonard-Louis, S.; Laura, M.; Blake, J.; Parman, Y.; Battaloglu, E.; Tazir, M.; Bellatache, M.; Bonello-Palot, N.; Levy, N.; Sacconi, S.; Guimaraes-Costa, R.; Attarian, S.; Latour, P.; Sole, G.; Megarbane, A.; Horvath, R.; Ricci, G.; Choi, B. -O.; Schenone, A.; Gemelli, C.; Geroldi, A.; Sabatelli, M.; Luigetti, M.; Santoro, L.; Manganelli, F.; Quattrone, A.; Valentino, P.; Murakami, T.; Scherer, S. S.; Dankwa, L.; Shy, M. E.; Bacon, C. J.; Herrmann, D. N.; Zambon, A.; Tramacere, I.; Pisciotta, C.; Magri, S.; Previtali, S. C.; Bolino, A. | |
| A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation. | 1-gen-2015 | Scarlato, M; Nuara, A; Gerevini, S; Benedetti, S; P., Rossi; Ferrari, Maurizio; Previtali, S. C. | |
| A novel heat shock protein 27 homozygous mutation: widening of the continuum between MND/dHMN/CMT2 | 1-gen-2015 | Scarlato, M; Vigano, F; Carrera, P; Previtali, Sc; Bolino, A | |
| A whole-brain network analysis in patients with hereditary and acquired peripheral neuropathy | 1-gen-2012 | Rocca, Ma; Valsasina, P; Fazio, R; Previtali, S; Falini, A; Comi, G; Filippi, M | |
| Alteration of the late endocytic pathway in Charcot-Marie-Tooth type 2B disease | 1-gen-2020 | Romano, R; Rivellini, C; De Luca, M; Tonlorenzi, R; Beli, R; Manganelli, F; Nolano, M; Santoro, L; Eskelinen, El; Previtali, S; Bucci, C | |
| Analyzing histopathological features of rare charcot-marie-tooth neuropathies to unravel their pathogenesis | 1-gen-2010 | Benedetti, S; Previtali, Sc; Coviello, S; Scarlato, M; Cerri, F; DI PIERRI, E; Piantoni, L; Spiga, I; Fazio, R; Riva, N; NATALI SORA, Mg; Dacci, P; Malaguti, Mc; Munerati, E; Grimaldi, Lm; Marrosu, Mg; DE PELLEGRIN, M; Ferrari, Maurizio; Comi, Giancarlo; Quattrini, A; Bolino, A. | |
| Animal Models as a Tool to Design Therapeutical Strategies for CMT-like Hereditary Neuropathies | 1-gen-2021 | Bosco, L; Falzone, Ym; Previtali, S | |
| Autocrine and immune cell-derived BDNF in human skeletal muscle: implications for myogenesis and tissue regeneration | 1-gen-2013 | Colombo, E; Bedogni, F; Lorenzetti, I; Landsberger, N; Previtali, S; Farina, C. | |
| Begelomab for severe refractory dermatomyositis: A case report | 1-gen-2021 | De Lorenzo, R.; Sciorati, C.; Monno, A.; Cavalli, S.; Bonomi, F.; Tronci, S.; Previtali, S.; Rovere-Querini, P. | |
| Brain connectivity abnormalities extend beyond the sensorimotor network in peripheral neuropathy | 1-gen-2014 | Rocca, Ma; Valsasina, P; Fazio, R; Previtali, Sc; Messina, R; Falini, Andrea; Comi, Giancarlo; Filippi, Massimo | |
| Cardiac and Neuromuscular Features of Patients with LMNA-Related Cardiomyopathy | 1-gen-2019 | Peretto, Giovanni; Di Resta, Chiara; Perversi, Jacopo; Forleo, Cinzia; Maggi, Lorenzo; Politano, Luisa; Barison, Andrea; Previtali, Stefano C; Carboni, Nicola; Brun, Francesca; Pegoraro, Elena; D'Amico, Adele; Rodolico, Carmelo; Magri, Francesca; Manzi, Rosa C; Palladino, Alberto; Isola, Franco; Gigli, Lorenzo; Mongini, Tiziana E; Semplicini, Claudio; Calore, Chiara; Ricci, Giulia; Comi, Giacomo P; Ruggiero, Lucia; Bertini, Enrico; Bonomo, Paolo; Nigro, Gerardo; Resta, Nicoletta; Emdin, Michele; Favale, Stefano; Siciliano, Gabriele; Santoro, Lucio; Sinagra, Gianfranco; Limongelli, Giuseppe; Ambrosi, Alessandro; Ferrari, Maurizio; Golzio, Pier G; Bella, Paolo Della; Benedetti, Sara; Sala, Simone | |
| Categorizing natural history trajectories of ambulatory function measured by the 6-minute walk distance in patients with Duchenne muscular dystrophy | 1-gen-2016 | Mercuri, E; Signorovitch, Je; Swallow, E; Song, J; Ward, Sj; Pane, M1; Mazzone, E; Messina, S; Vita, Gl; Sormani, Mp; D'Amico, A; Berardinelli, A; Magri, F; Comi, Gp; Baranello, G; Mongini, T; Pini, A; Battini, R; Pegoraro, E; Bruno, C; Politano, L; Previtali, S; Binks, Mh; Campion, G; Charnas, L; Kaye, E; Kelly, M; Morris, C; Reha, A; Trajectory Analysis Project, (cTAP) | |
| Charcot-Marie-Tooth type 4B demyelinating neuropathy: deciphering the role of MTMR phosphatases | 1-gen-2007 | Previtali, S; Quattrini, A; Bolino, A | |
| CSN5/JAB1 PLAYS A ROLE IN AXONAL SORTING AND MYELINATION IN PERIPHERAL NERVE | 1-gen-2012 | Porrello, E; Rivellini, C; Dina, G; Triolo, D; Pardi, R; Wrabetz, L; Feltri, Ml; Quattrini, A; Previtali, S | |
| CSN5/JAB1 REGULATES SCHWANN CELL-AXON INTERACTION AND PLAYS A ROLE IN PERIPHERAL NERVE DEVELOPMENT AND FUNCTION | 1-gen-2009 | Porrello, E; Cerri, F; Dina, G; Triolo, D; Lopez, Id; Panattoni, M; Del Carro, U; Morana, P; Comi, G; Wrabetz, L; Feltri, Ml; Pardi, R; Quattrini, A; Previtali, S | |
| DEFINING GENOTYPE-PHENOTYPE CORRELATIONS IN THE CMT NEUROPATHIES | 1-gen-2009 | Benedetti, S; Coviello, S; Colombo, A; Piantoni, L; Spiga, I; Cerri, F; Scarlato, M; Fazio, R; Quattrini, A; Previtali, Sc; Bolino, A | |
| Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements | 1-gen-2017 | D'Amico, A; Catteruccia, M; Baranello, G; Politano, L; Govoni, A; Previtali, S; Pane, M; D'Angelo, Mg; Bruno, C; Messina, S; Ricci, F; Pegoraro, E; Pini, A; Berardinelli, A; Gorni, K; Battini, R; Vita, G; Trucco, F; Scutifero, M; Petillo, R; D'Ambrosio, P; Ardissone, A; Pasanisi, B; Vita, G; Mongini, T; Moggio, M; Comi, Gp; Mercuri, E; Bertini, E |