Atypical onset in a series of 122 cases with FacioScapuloHumeral Muscular Dystrophy von Pastorello, Ebe, Cao, Michelangelo, Trevisan, Carlo P

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Facioscapulohumeral Muscular Dystrophy: A Multicenter Study on Hearing Function von Trevisan, Carlo P., Pastorello, Ebe, Ermani, Mario, Angelini, Corrado, Tomelleri, Giuliano, Tonin, Paola, Mongini, Tiziana, Palmucci, Laura, Galluzzi, Giuliana, Tupler, Rossella G., Marioni, Gino, Rimini, Alessandro

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Dominant muscular dystrophy with a novel SYNE1 gene mutation von Fanin, Marina, Savarese, Marco, Nascimbeni, Anna C., Di Fruscio, Giuseppina, Pastorello, Ebe, Tasca, Elisabetta, Trevisan, Carlo P., Nigro, Vincenzo, Angelini, Corrado

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Liver transplantation for Wilson's disease: The burden of neurological and psychiatric disorders von Medici, Valentina, Mirante, Vincenzo G., Fassati, Luigi R., Pompili, Maurizio, Forti, Domenico, Del Gaudio, Massimo, Trevisan, Carlo P., Cillo, Umberto, Sturniolo, Giacomo C., Fagiuoli, Stefano

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Undiagnosed myopathy before surgery and safe anaesthesia table von Trevisan, Carlo P, Accorsi, Alma, Morandi, Lucia O, Mongini, Tiziana, Savoia, Gennaro, Gravino, Elvira, Angelini, Corrado, Tegazzin, Vincenzo

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Ataxia and Congenital Muscular Dystrophy: the follow-up of a new specific phenotype von Trevisan, Carlo P, Pastorello, Ebe, Tonello, Simone, Armani, Mario, Rigoni, Maria T, Tormene, Alma P, Freda, Maria P, Zortea, Michela, Lombardi, Stefania

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Integrin α7β1 in Muscular Dystrophy/Myopathy of Unknown Etiology von Pegoraro, Elena, Cepollaro, Fulvio, Prandini, Paola, Marin, Alessandra, Fanin, Marina, Trevisan, Carlo P., El-Messlemani, Abdul Hassib, Tarone, Guido, Engvall, Eva, Hoffman, Eric P., Angelini, Corrado

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Tau missing from csf : a case report von ALBERICI, Antonella, ARMANI, Mario, TREVISAN, Carlo P, GROWDON, John H, BORRONI, Barbara, PADOVANI, Alessandro, ROSSINI, Paolo M, BINETTI, Giuliano, PATERLINI, Anna, BENUSSI, Luisa, FRANCESCA NICOSIA, GHIDONI, Roberta, SIGNORINI, Simona, COTELLI, Maria, FRISONI, Giovanni B, GEROLDI, Cristina

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Clinical and molecular study in congenital muscular dystrophy with partial laminin ?2 (LAMA2) deficiency von Tezak, Zivana, Prandini, Paola, Boscaro, Marco, Marin, Alessandra, Devaney, Joseph, Marino, Michael, Fanin, Marina, Trevisan, Carlo P., Park, Julie, Tyson, Weslie, Finkel, R., Garcia, Carlos, Angelini, Corrado, Hoffman, Eric P., Pegoraro, Elena

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Novel mutations and polymorphisms in the human dystrophin gene detected by double-strand conformation analysis von Saad, Fawzy A., Mostacciuolo, Maria L., Trevisan, Carlo P., Tomelleri, Giuliano, Angelini, Corrado, Salam, Ekram Abdel, Danieli, Gian Antonio

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Clinical and molecular study in congenital muscular dystrophy with partial laminin α2 (LAMA2) deficiency von Tezak, Zivana, Prandini, Paola, Boscaro, Marco, Marin, Alessandra, Devaney, Joseph, Marino, Michael, Fanin, Marina, Trevisan, Carlo P., Park, Julie, Tyson, Weslie, Finkel, R., Garcia, Carlos, Angelini, Corrado, Hoffman, Eric P., Pegoraro, Elena

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Integrin alpha 7 beta 1 in muscular dystrophy/myopathy of unknown etiology von Pegoraro, Elena, Cepollaro, Fulvio, Prandini, Paola, Marin, Alessandra, Fanin, Marina, Trevisan, Carlo P, El-Messlemani, Abdul Hassib, Tarone, Guido, Engvall, Eva, Hoffman, Eric P, Angelini, Corrado

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Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency von Tezak, Zivana, Prandini, Paola, Boscaro, Marco, Marin, Alessandra, Devaney, Joseph, Marino, Michael, Fanin, Marina, Trevisan, Carlo P, Park, Julie, Tyson, Weslie, Finkel, R, Garcia, Carlos, Angelini, Corrado, Hoffman, Eric P, Pegoraro, Elena

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Genetic epidemiology of congenital muscular dystrophy in a sample from north-east Italy von MOSTACCIUOLO, M. L, MIORIN, M, MARTINELLO, F, ANGELINI, C, PERINI, P, TREVISAN, C. P

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Long term experience in Wilson disease treatment von Medici, Valentina, D'Inca, Renata, Barollo, Michela, Trevisan, Carlo P., Zancan, Lucia, Sturniolo, Giacomo C.

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Integrin {alpha}7{beta}1 in Muscular Dystrophy/Myopathy of Unknown Etiology von Pegoraro, Elena, Cepollaro, Fulvio, Prandini, Paola, Marin, Alessandra, Fanin, Marina, Trevisan, Carlo P, El-Messlemani, Abdul Hassib, Tarone, Guido, Engvall, Eva, Hoffman, Eric P, Angelini, Corrado

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Prenatal diagnosis in congenital muscular dystrophy von Muntoni, Francesco, Sewry, Caroline, Wilson, Lesley, Angelini, Corrado, Trevisan, CarloP, Brambati, Bruno, Dubowitz, Victor

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Brain alterations in the classical form of congenital muscular dystrophy : Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle von TREVISAN, C. P, MARTINELLO, F, FERRUZZA, E, FANIN, M, CHEVALLAY, M, TOME, F. M. S

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Prevalence of unsuspected myopathy in infants presenting for clubfoot surgery von ZANETTE, GASTONE, MANANI, GIOVANNI, PITTONI, GIOVANNI, ANGELINI, CORRADO, TREVISAN, CARLO P., TURRA, SISTO

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Reversible aphasia in adolescence: A late-onset form of Landau Kleffner syndrome? Report of a single case von Denes, G, Mantovan, C, Ferruzza, E, Trevisan, C P, Gallo, A

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