Sfoglia per Autore
Dominant muscular dystrophy with a novel SYNE1 gene mutation
2015 Fanin, M.; Savarese, M.; Nascimbeni, A. C.; Di Fruscio, G.; Pastorello, E.; Tasca, E.; Trevisan, C. P.; Nigro, V.; Angelini, C.
Undiagnosed myopathy before surgery and safe anaesthesia table
2013 Trevisan, Cp; Accorsi, A; Morandi, Lo; Mongini, T; Savoia, G; Gravino, E; Angelini, C; Tegazzin, V; Trevisan, Cp; Accorsi, A; Morandi, Lo; Mongini, T; Savoia, G; Gravino, E; Angelini, C; Tegazzin, V; Trevisan, Cp; Accorsi, A; Morandi, Lo; Mongini, T; Savoia, G; Gravino, E; Angelini, C; Tegazzin, V; Trevisan, Cp; Accorsi, A; Morandi, Lo; Mongini, T; Savoia, G; Gravino, E; Angelini, C; Tegazzin, V; Trevisan, Cp; Accorsi, A; Morandi, Lo; Mongini, T; Savoia, G; Gravino, E; Angelini, C; Tegazzin, V; Trevisan, Cp; Accorsi, A; Morandi, Lo; Mongini, T; Savoia, G; Gravino, E; Angelini, C; Tegazzin, V; Trevisan, Cp; Accorsi, A; Morandi, Lo; Mongini, T; Savoia, G; Gravino, E; Angelini, C; Tegazzin, V; Trevisan, Cp; Accorsi, A; Morandi, Lo; Mongini, T; Savoia, G; Gravino, E; Angelini, C; Tegazzin, V; Trevisan, Cp; Accorsi, A; Morandi, Lo; Mongini, T; Savoia, G; Gravino, E; Angelini, C; Tegazzin, V; Trevisan, Cp; Accorsi, A; Morandi, Lo; Mongini, T; Savoia, G; Gravino, E; Angelini, C; Tegazzin, V; Trevisan, Cp; Accorsi, A; Morandi, Lo; Mongini, T; Savoia, G; Gravino, E; Angelini, C; Tegazzin, V
Spinal Cord Herniation: A Missing Piece in the Pathogenesis of Amyotrophic Lateral Sclerosis and Multiple Sclerosis?
2011 Manara, Renzo; Citton, Valentina; Nardetto, Lucia; Semplicini, Claudio; Burlina, Alessandro; Trevisan, CARLO PIETRO; Argentiero, Vincenza; Baracchini, Claudio
Missplicing of Troponin T transcripts in Myotonic dystrophy type 2 human biopsies
2010 Salvatori, Sergio; Picard, ANNE ALEIDA; Furlan, S; Fanin, Marina; Trevisan, CARLO PIETRO; Angelini, Corrado
Brain involvement in myotonic dystrophies: neuroimaging and neuropsychological comparative study in DM1 and DM2
2010 Romeo, V; Pegoraro, Elena; Ferrati, C; Squarzanti, F; Soraru', Gianni; Palmieri, Arianna; Zucchetta, P; Antunovic, L; Bonifazi, E; Novelli, G; Trevisan, CARLO PIETRO; Ermani, Mario; Manara, R; Angelini, Corrado
Congenital muscular dystrophies with defective glycosylation of dystroglycan: apopulation study
2009 Mercuri, E; Messina, S; Bruno, C; Mora, M; Pegoraro, Elena; Comi, Gp; D'Amico, A; Aiello, C; Biancheri, R; Berardinelli, A; Boffi, P; Cassandrini, D; Laverda, ANNA MARIA; Moggio, M; Morandi, L; Moroni, I; Pane, M; Pezzani, Raffaele; Pichiecchio, A; Pini, A; Minetti, C; Mongini, T; Mottarelli, E; Ricci, E; Ruggieri, A; Saredi, S; Scuderi, C; Tessa, A; Toscano, A; Tortorella, G; Trevisan, CARLO PIETRO; Uggetti, C; Vasco, G; Santorelli, Fm; Bertini, E.
Comparative transcriptional and biochemical studies in muscle of myotonic dystrophies (DM1 and DM2)
2009 Salvatori, Sergio; Furlan, S; Fanin, Marina; Picard, ANNE ALEIDA; Pastorello, Ebe; Romeo, Vincenzo; Trevisan, CARLO PIETRO; Angelini, Corrado
Study of atrophy factors in 7 patients with myotonic dystrophy type 2
2009 Marsala, Sz; Fanin, Marina; Pegoraro, Elena; Trevisan, CARLO PIETRO; Marchini, C; Angelini, Corrado
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample
2009 Mostacciuolo, MARIA LUISA; Pastorello, E; Vazza, Giovanni; Miorin, M; Angelini, Corrado; Tomelleri, G; Galluzzi, G; Trevisan, CARLO PIETRO
Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions
2008 Trevisan, CARLO PIETRO; Pastorello, Ebe; G., Tomelleri; L., Vercelli; C., Bruno; S., Scapolan; G., Siciliano; F., Comacchio
POMT1 and POMT2 mutations in CMD patients: A multicentric Italian study
2008 Messina, S; Mora, M; Pegoraro, Elena; Pini, A; Mongini, T; D'Amico, A; Pane, M; Aiello, C; Bruno, C; Biancheri, R; Berardinelli, A; Boito, C; Farina, L; Morandi, L; Moroni, I; Pezzani, Raffaele; Pichiecchio, A; Ricci, E; Ruggieri, A; Saredi, S; Scuderi, C; Tessa, A; Toscano, A; Tortorella, G; Trevisan, CARLO PIETRO; Uggetti, C; Santorelli, Fm; Bertini, E; Mercuri, E.
Phenotypic clustering of lamin A/C mutations in neuromuscular patients
2007 Benedetti, S; Menditto, I; Degano, M; Rodolico, C; Merlini, L; D'Amico, A; Palmucci, L; Berardinelli, A; Pegoraro, Elena; Trevisan, CARLO PIETRO; Morandi, L; Moroni, I; Galluzzi, G; Bertini, E; Toscano, A; Olive, M; Bonne, G; Mari, F; Caldara, R; Fazio, R; Mammii, I; Carrera, P; Toniolo, D; Comi, G; Quattrini, A; Ferrari, M; Previtali, Sc
Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia
2006 Crippa, F; Panzeri, C; Martinuzzi, Andrea; Arnoldi, A; Redaelli, F; Tonelli, A; Baschirotto, C; Vazza, Giovanni; Mostacciuolo, MARIA LUISA; Daga, A; Orso, G; Profice, P; Trabacca, A; D'Angelo, Mg; Comi, Gp; Galbiati, S; Lamperti, C; Bonato, S; Pandolfo, M; Meola, G; Musumeci, O; Toscano, A; Trevisan, CARLO PIETRO; Bresolin, N; Bassi, Mt
Exploring mental status in Friedreich's ataxia: a combined neuropsychological, behavioral and neuroimaging study.
2006 Mantovan, Mc; Martinuzzi, A; Squarzanti, F; Bolla, A; Silvestri, I; Liessi, G; Macchi, Carlo; Ruzza, G; Trevisan, CARLO PIETRO; Angelini, Corrado
Diagnosis and management of Wilson's disease - Results of a single center experience
2006 Medici, V; Trevisan, CARLO PIETRO; D'Inca', R; Barollo, M; Zancan, L; Fagiuoli, S; Martines, Diego; Irato, Paola; Sturniolo, Giacomo
Facioscapulohumeral muscular dystrophy and occurrence of heart arrhythmia
2006 Trevisan, CARLO PIETRO; Pastorello, E; Armani, M; Angelini, Corrado; Nante, G; Tomelleri, G; Tonin, P; Mongini, T; Palmucci, L; Galluzzi, G; Tupler, Rg; Barchitta, A.
Adverse reaction after tetrathiomolybdate treatment for Wilson's disease: A case report
2006 Medici, V; Trevisan, CARLO PIETRO; Bigotto, Ma; D'Inca, R; Martines, Diego; DAL PONT, E; Sturniolo, Giacomo
Molecular and clinical characterization of a large cohort of Italian patients with Hereditary Spastic Paraplegia (HSP)
2006 Martinuzzi, A; Rossetto, Mg; Crippa, F; Panzeri, C; Musumeci, O; Vazza, Giovanni; Toscano, A; Comi, Gp; Dangelo, G; Mostacciuolo, MARIA LUISA; Trevisan, CARLO PIETRO; Siciliano, G; Meola, G; Profice, P; Daga, A; Pandolfo, M; Bresolin, N; Bassi, Mt
Decreased expression of DMPK: correlation with CTG repeat expansion and fibre type composition in myotonic dystrophy type 1
2005 Salvatori, Sergio; Fanin, Marina; Trevisan, CARLO PIETRO; Furlan, S; Reddy, S; Nagy, Ji; Angelini, Corrado
Liver transplantation for Wilson's disease: The burden of neurological and psychiatric disorders
2005 Medici, Valentina; MIRANTE V., G; FASSATI L., R; Pompili, M; Forti, D; DEL GAUDIO, M; Trevisan, CARLO PIETRO; Cillo, Umberto; Sturniolo, Giacomo; Fagiuoli, S.
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