TREVISAN, CARLO PIETRO
TREVISAN, CARLO PIETRO
A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy.
2000 Pegoraro, Elena; Fanin, Marina; Trevisan, CARLO PIETRO; Angelini, Corrado; Hoffman, E. P.
A severe case of Duchenne-like muscular dystrophy due to a mutation in the alpha-sarcoglycan (adhalin) gene
1996 Fanin, Marina; Martinello, F; Duggan, Dj; Gorospe, Jr; Freda, Mp; Pegoraro, Elena; Soraru', Gianni; Mostacciuolo, MARIA LUISA; Trevisan, CARLO PIETRO; Hoffman, Ep; Angelini, Corrado
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
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
Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency
2003 Tezak, Z; Prandini, P; Boscaro, Marco; Marin, A; Devaney, J; Marino, M; Fanin, Marina; Trevisan, CARLO PIETRO; Park, J; Tyson, W; Finkel, R; Garcia, C; Angelini, Corrado; Hoffman, Ep; Pegoraro, Elena
Clinical varieties of carnitine and carnitine palmitoyltransferase deficiency
1987 Angelini, C.; Trevisan, C.; Isaya, G.; Pegolo, G.; Vergani, L.
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
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.
CTG repeat expansion and fiber type composition affect DMPK expression in myotonic dystrophy type 1.
2004 Salvatori, Sergio; Fanin, Marina; Trevisan, CARLO PIETRO; Furlan, S.; Reddy, S.; Angelini, Corrado
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
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
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.
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
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.
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
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1
2002 Zortea, M.; Vettori, Andrea; Trevisan, CARLO PIETRO; Bellini, S.; Vazza, Giovanni; Armani, Mario; Simonati, A.; Mostacciuolo, MARIA LUISA
Integrin alpha 7 beta 1 in muscular dystrophy/myopathy of unknown etiology
2002 Pegoraro, Elena; Cepollaro, F; Prandini, P; Marin, A; Fanin, Marina; Trevisan, CARLO PIETRO; EL MESSLEMANI, Ah; Tarone, G; Engvall, E; Hoffman, Ep; Angelini, Corrado
Integrin α7β1 in muscular dystrophy/myopathy of unknown etiology
2002 Pegoraro, E.; Cepollaro, F.; Prandini, P.; Marin, A.; Fanin, M.; Trevisan, C. P.; El-Messlemani, A. H.; Tarone, G.; Engvall, E.; Hoffman, E. P.; Angelini, C.