Osteopontin is highly expressed in severely dystrophic muscle and seems to play a role in muscle regeneration and fibrosis von Zanotti, Simona, Gibertini, Sara, Di Blasi, Claudia, Cappelletti, Cristina, Bernasconi, Pia, Mantegazza, Renato, Morandi, Lucia, Mora, Marina

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Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients von Guglieri, Michela, Magri, Francesca, D'Angelo, Maria Grazia, Prelle, Alessandro, Morandi, Lucia, Rodolico, Carmelo, Cagliani, Rachele, Mora, Marina, Fortunato, Francesco, Bordoni, Andreina, Del Bo, Roberto, Ghezzi, Serena, Pagliarani, Serena, Lucchiari, Sabrina, Salani, Sabrina, Zecca, Chiara, Lamperti, Costanza, Ronchi, Dario, Aguennouz, Mohammed, Ciscato, Patrizia, Di Blasi, Claudia, Ruggieri, Alessandra, Moroni, Isabella, Turconi, Anna, Toscano, Antonio, Moggio, Maurizio, Bresolin, Nereo, Comi, Giacomo P

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Decorin and biglycan expression is differentially altered in several muscular dystrophies von Zanotti, Simona, Negri, Tiziana, Cappelletti, Cristina, Bernasconi, Pia, Canioni, Eleonora, Di Blasi, Claudia, Pegoraro, Elena, Angelini, Corrado, Ciscato, Patrizia, Prelle, Alessandro, Mantegazza, Renato, Morandi, Lucia, Mora, Marina

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LAMA2 stop-codon mutation: Merosin-deficient congenital muscular dystrophy with occipital polymicrogyria, epilepsy and psychomotor regression von Vigliano, Piernanda, Dassi, Patrizia, Blasi, Claudia Di, Mora, Marina, Jarre, Laura

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Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2 von Di Blasi, Claudia, Bellafiore, Emanuela, Salih, Mustafa Am, Manzini, M Chiara, Moore, Steven A, Seidahmed, Mohammed Z, Mukhtar, Maowia M, Karrar, Zein A, Walsh, Christopher A, Campbell, Kevin P, Mantegazza, Renato, Morandi, Lucia, Mora, Marina

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Abnormal lysosomal and ubiquitin-proteasome pathways in 19p13.3 distal myopathy von Di Blasi, Claudia, Moghadaszadeh, Behzad, Ciano, Claudia, Negri, Tiziana, Giavazzi, Alessio, Cornelio, Ferdinando, Morandi, Lucia, Mora, Marina

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Transforming growth factor- β1 and fibrosis in congenital muscular dystrophies von Bernasconi, Pia, Di Blasi, Claudia, Mora, Marina, Morandi, Lucia, Galbiati, Silvia, Confalonieri, Paolo, Cornelio, Ferdinando, Mantegazza, Renato

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Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping von Di Blasi, Claudia, He, Yi, Morandi, Lucia, Cornelio, Ferdinando, Guicheney, Pascale, Mora, Marina

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Severe Congenital Muscular Dystrophy in a LAMA2 -Mutated Case von Di Blasi, Claudia, PhD, van Alfen, Nens, MD, PhD, Colleoni, Francesca, PhD, ter Laak, Henk, MSc, PhD, Mora, Marina, PhD

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Partial laminin α2 chain deficiency in a patient with myopathy resembling inclusion body myositis von Di Blasi, Claudia, Mora, Marina, Pareyson, Davide, Farina, Laura, Sghirlanzoni, Angelo, Vignier, Nicolas, Blasevich, Flavia, Cornelio, Ferdinando, Guicheney, Pascale, Morandi, Lucia

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A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemia von Di Blasi, Claudia, Sansanelli, Serena, Ruggieri, Alessandra, Moriggi, Manuela, Vasso, Michele, D'Adamo, Adamo Pio, Blasevich, Flavia, Zanotti, Simona, Paolini, Cecilia, Protasi, Feliciano, Tezzon, Frediano, Gelfi, Cecilia, Morandi, Lucia, Pessia, Mauro, Mora, Marina

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Concomitant deficiency of β- and γ-sarcoglycans in 20 α-sarcoglycan (adhalin)-deficient patients : immunohistochemical analysis and clinical aspects von BARRESI, R, CONFALONIERI, V, PINI, A, CORNELIO, F, MORA, M, MORANDI, L, LANFOSSI, M, DI BLASI, C, TORCHIANA, E, MANTEGAZZA, R, JARRE, L, NARDOCCI, N, BOFFI, P, TEZZON, F

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Osteopontin is highly expressed in severely dystrophic muscle and seems to play a role in muscle regeneration and fibrosis: Fibrosis in muscular dystrophies von Zanotti, Simona, Gibertini, Sara, Di Blasi, Claudia, Cappelletti, Cristina, Bernasconi, Pia, Mantegazza, Renato, Morandi, Lucia, Mora, Marina

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Danon disease: A novel LAMP2 mutation affecting the pre-mRNA splicing and causing aberrant transcripts and partial protein expression von Di Blasi, Claudia, Jarre, Laura, Blasevich, Flavia, Dassi, Patrizia, Mora, Marina

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Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by β sarcoglycan mutations von Barresi, Rita, Di Blasi, Claudia, Negri, Tiziana, Brugnoni, Raffaella, Vitali, Andrea, Felisari, Giorgio, Salandi, Antonio, Daniel, Sergio, Cornelio, Ferdinando, Morandi, Lucia, Mora, Marina

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Calsequestrin and junctin immunoreactivity in hexagonally cross-linked tubular arrays myopathy von Di Blasi, Claudia, Blasevich, Flavia, Bellafiore, Emanuela, Mottarelli, Elisa, Gibertini, Sara, Zanotti, Simona, Saredi, Simona, Mantegazza, Renato, Morandi, Lucia, Mora, Marina

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Heart-Specific Localization of Emerin: New Insights Into Emery-Dreifuss Muscular Dystrophy von Cartegni, Luca, di Barletta, Marina Raffaele, Barresi, Rita, Squarzoni, Stefano, Sabatelli, Patrizia, Maraldi, Nadir, Mora, Marina, Di Blasi, Claudia, Cornelio, Ferdinando, Merlini, Luciano, Villa, Antonello, Cobianchi, Fabio, Toniolo, Daniela

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Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalities von Mora, Marina, Moroni, Isabella, Uziel, Graziella, Di Blasi, Claudia, Barresi, Rita, Farina, Laura, Morandi, Lucia

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Partial laminin ?2 chain deficiency in a patient with myopathy resembling inclusion body myositis von Di Blasi, Claudia, Mora, Marina, Pareyson, Davide, Farina, Laura, Sghirlanzoni, Angelo, Vignier, Nicolas, Blasevich, Flavia, Cornelio, Ferdinando, Guicheney, Pascale, Morandi, Lucia

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Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by [beta] sarcoglycan mutations von Barresi, Rita, Di Blasi, Claudia, Negri, Tiziana, Brugnoni, Raffaella, Vitali, Andrea, Felisari, Giorgio, Salandi, Antonio, Daniel, Sergio, Cornelio, Ferdinando, Morandi, Lucia, Mora, Marina

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