A systematic review on the definition of rhabdomyolysis von Stahl, Kristina, Rastelli, Emanuele, Schoser, Benedikt

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Validation of Motor Outcome Measures in Myotonic Dystrophy Type 2 von Montagnese, Federica, Rastelli, Emanuele, Khizanishvili, Nina, Massa, Roberto, Stahl, Kristina, Schoser, Benedikt

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Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients von Pennisi, Elena Maria, Arca, Marcello, Bertini, Enrico, Bruno, Claudio, Cassandrini, Denise, D'amico, Adele, Garibaldi, Matteo, Gragnani, Francesca, Maggi, Lorenzo, Massa, Roberto, Missaglia, Sara, Morandi, Lucia, Musumeci, Olimpia, Pegoraro, Elena, Rastelli, Emanuele, Santorelli, Filippo Maria, Tasca, Elisabetta, Tavian, Daniela, Toscano, Antonio, Angelini, Corrado

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Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis von Campione, Elena, MD, PhD, Botta, Annalisa, PhD, Di Prete, Monia, MD, Rastelli, Emanuele, MD, Gibellini, Manuela, MD, Petrucci, Antonio, MD, Bernardini, Sergio, MD, Novelli, Giuseppe, PhD, Bianchi, Luca, MD, Orlandi, Augusto, MD, Massa, Roberto, MD, Terracciano, Chiara, MD, PhD

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An Age-Standardized Prevalence Estimate and a Sex and Age Distribution of Myotonic Dystrophy Types 1 and 2 in the Rome Province, Italy von Vanacore, Nicola, Rastelli, Emanuele, Antonini, Giovanni, Bianchi, Maria Laura Ester, Botta, Annalisa, Bucci, Elisabetta, Casali, Carlo, Costanzi-Porrini, Sandro, Giacanelli, Manlio, Gibellini, Manuela, Modoni, Anna, Novelli, Giuseppe, Pennisi, Elena Maria, Petrucci, Antonio, Piantadosi, Carlo, Silvestri, Gabriella, Terracciano, Chiara, Massa, Roberto

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How to capture activities of daily living in myotonic dystrophy type 2? von Montagnese, Federica, Rastelli, Emanuele, Stahl, Kristina, Massa, Roberto, Schoser, Benedikt

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Towards clinical outcome measures in myotonic dystrophy type 2: a systematic review von Rastelli, Emanuele, Montagnese, Federica, Massa, Roberto, Schoser, Benedikt

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Aquaporin 4 expression in human skeletal muscle fiber types von Vizzaccaro, Elisa, Terracciano, Chiara, Rastelli, Emanuele, Massa, Roberto

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Comparative Sleep Disturbances in Myotonic Dystrophy Types 1 and 2 von Romigi, Andrea, Franco, Valentina, Placidi, Fabio, Liguori, Claudio, Rastelli, Emanuele, Vitrani, Giuseppe, Centonze, Diego, Massa, Roberto

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Prevalence and predictor factors of respiratory impairment in a large cohort of patients with Myotonic Dystrophy type 1 (DM1): A retrospective, cross sectional study von Rossi, Salvatore, Della Marca, Giacomo, Ricci, Martina, Perna, Alessia, Nicoletti, Tommaso F., Brunetti, Valerio, Meleo, Emiliana, Calvello, Mariarosaria, Petrucci, Antonio, Antonini, Giovanni, Bucci, Elisabetta, Licchelli, Loretta, Sancricca, Cristina, Massa, Roberto, Rastelli, Emanuele, Botta, Annalisa, Di Muzio, Antonio, Romano, Sonia, Garibaldi, Matteo, Silvestri, Gabriella

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Neutral lipid-storage disease with myopathy and extended phenotype with novel PNPLA2 mutation von Massa, Roberto, Pozzessere, Simone, Rastelli, Emanuele, Serra, Laura, Terracciano, Chiara, Gibellini, Manuela, Bozzali, Marco, Arca, Marcello

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Understanding hyper-reflexia in acute motor axonal neuropathy (AMAN) von Versace, Viviana, Campostrini, Stefania, Rastelli, Emanuele, Sebastianelli, Luca, Nardone, Raffaele, Pucks-Faes, Elke, Saltuari, Leopold, Kofler, Markus, Uncini, Antonino

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Validation of the Nine Hole Peg Test as a measure of dexterity in myotonic dystrophy type 1 von Cutellè, Claudia, Rastelli, Emanuele, Gibellini, Manuela, Greco, Giulia, Frezza, Erica, Botta, Annalisa, Terracciano, Chiara, Massa, Roberto

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Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factors von Bianchi, Maria Laura Ester, Leoncini, Emanuele, Masciullo, Marcella, Modoni, Anna, Gadalla, Shahinaz M., Massa, Roberto, Rastelli, Emanuele, Terracciano, Chiara, Antonini, Giovanni, Bucci, Elisabetta, Petrucci, Antonio, Costanzi, Sandro, Santoro, Massimo, Boccia, Stefania, Silvestri, Gabriella

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Thymomatous myasthenia gravis: novel association with HLA DQB105:01 and strengthened evidence of high clinical and serological severity von Massa, Roberto, Greco, Giulia, Testi, Manuela, Rastelli, Emanuele, Terracciano, Chiara, Frezza, Erica, Garibaldi, Matteo, Marfia, Girolama A., Locatelli, Franco, Mercuri, Nicola B., Pompeo, Eugenio, Antonini, Giovanni, Andreani, Marco

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Periodic acid-Schiff staining on resin muscle sections: Improvement in the histological diagnosis of late-onset Pompe disease von Terracciano, Chiara, Rastelli, Emanuele, Massa, Roberto

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Vitamin D deficiency in myotonic dystrophy type 1 von Terracciano, Chiara, Rastelli, Emanuele, Morello, Maria, Celi, Monica, Bucci, Elisabetta, Antonini, Giovanni, Porzio, Ottavia, Tarantino, Umberto, Zenobi, Rossella, Massa, Roberto

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Reply to the letter entitled “Predictors of respiratory impairment in patients with myotonic dystrophy type 1” von Rossi, Salvatore, Della Marca, Giacomo, Ricci, Martina, Perna, Alessia, Nicoletti, Tommaso F., Brunetti, Valerio, Meleo, Emiliana, Calvello, Mariarosaria, Petrucci, Antonio, Antonini, Giovanni, Bucci, Elisabetta, Licchelli, Loretta, Sancricca, Cristina, Massa, Roberto, Rastelli, Emanuele, Botta, Annalisa, Di Muzio, Antonio, Romano, Sonia, Garibaldi, Matteo, Silvestri, Gabriella

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RECURRENT HYPERCKEMIA WITH NORMAL MUSCLE BIOPSY IN A PEDIATRIC PATIENT WITH NEUROMYELITIS OPTICA von DI FILIPPO, Massimiliano, FRANCIOTTA, Diego, MENDUNO, Paola, FLORIDI, Piero, SARCHIELLI, Paola, CALABRESI, Paolo, MASSA, Roberto, DI GREGORIO, Maria, ZARDINI, Elisabetta, GASTALDI, Matteo, TERRACCIANO, Chiara, RASTELLI, Emanuele, GAETANI, Lorenzo, IANNONE, Alessia

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Erratum to: Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factors von Bianchi, Maria Laura Ester, Leoncini, Emanuele, Masciullo, Marcella, Modoni, Anna, Gadalla, Shahinaz M., Massa, Roberto, Botta, Annalisa, Rastelli, Emanuele, Terracciano, Chiara, Antonini, Giovanni, Bucci, Elisabetta, Petrucci, Antonio, Costanzi, Sandro, Santoro, Massimo, Boccia, Stefania, Silvestri, Gabriella

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