MyoD Expression Restores Defective Myogenic Differentiation of Human Mesoangioblasts from Inclusion-Body Myositis Muscle von Morosetti, Roberta, Mirabella, Massimiliano, Gliubizzi, Carla, Broccolini, Aldobrando, De Angelism, Luciana, Tagliafico, Enrico, Sampaolesi, Maurilio, Gidaro, Teresa, Papacci, Manuela, Roncaglia, Enrica, Rutella, Sergio, Ferrari, Stefano, Tonali, Pietro Attilio, Ricci, Enzo, Cossu, Giulio

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Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene von Perna, Alessia, Bosco, Luca, Fattori, Fabiana, Torchia, Eleonora, Modoni, Anna, Papacci, Manuela, Petrucci, Antonio, Tasca, Giorgio, Ricci, Enzo, Bertini, Enrico Silvio, Silvestri, Gabriella

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Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy von Lucchini, Matteo, Bortolani, Sara, Monforte, Mauro, Papacci, Manuela, Ricci, Enzo, Mirabella, Massimiliano, Tasca, Giorgio

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Apoptosis and ROS Detoxification Enzymes Correlate with Cytochrome c Oxidase Deficiency in Mitochondrial Encephalomyopathies von Di Giovanni, Simone, Mirabella, Massimiliano, Papacci, Manuela, Odoardi, Francesca, Silvestri, Gabriella, Servidei, Serenella

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Insulin-like Growth Factor I in Inclusion-Body Myositis and Human Muscle Cultures von BROCCOLINI, ALDOBRANDO, RICCI, ENZO, PESCATORI, MARIO, PAPACCI, MANUELA, GLIUBIZZI, CARLA, DʼAMICO, ADELE, SERVIDEI, SERENELLA, TONALI, PIETRO, MIRABELLA, MASSIMILIANO

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MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle von Morosetti, Roberta, Mirabella, Massimiliano, Gliubizzi, Carla, Broccolini, Aldobrando, De Angelis, Luciana, Tagliafico, Enrico, Sampaolesi, Maurilio, Gidaro, Teresa, Papacci, Manuela, Roncaglia, Enrica, Rutella, Sergio, Ferrari, Stefano, Tonali, Pietro Attilio, Ricci, Enzo, Cossu, Giulio

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Pathogenic role of mtDNA duplications in mitochondrial diseases associated with mtDNA deletions von Odoardi, Francesca, Rana, Michele, Broccolini, Aldobrando, Mirabella, Massimiliano, Modoni, Anna, D'Amico, Adele, Papacci, Manuela, Tonali, Pietro, Servidei, Serenella, Silvestri, Gabriella

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Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene von Perna, Alessia, Bosco, Luca, Fattori, Fabiana, Torchia, Eleonora, Modoni, Anna, Papacci, Manuela, Petrucci, Antonio, Tasca, Giorgio, Ricci, Enzo, Bertini, Enrico Silvio, Silvestri, Gabriella

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Peripheral neuropathy with giant axons and cardiomyopathy associated with desmin type intermediate filaments in skeletal muscle von Sabatelli, Mario, Bertini, Enrico, Ricci, Enzo, Salviati, Giovanni, Magi, Stefania, Papacci, Manuela, Tonali, Pietro

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Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a family von Manfredi, Giovanni, Silvestri, Gabriella, Servidei, Serenella, Ricci, Enzo, Mirabella, Massimiliano, Bertini, Enrico, Papacci, Manuela, Rana, Michele, Tonali, Pietro

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