An Italian Model for the Management of Cancer Patients during COVID-19 Pandemic: The Regional Center for Oncological Orientation (COrO) of Taranto (ROP) von Pisconti, Salvatore, Modoni, Gabriella, Cafiero, Concetta, Simeone, Giuseppe, Surico, Giammarco, Gorgoni, Giovanni

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Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression von Pescatori, Mario, Broccolini, Aldobrando, Minetti, Carlo, Bertini, Enrico, Bruno, Claudio, D'amico, Adele, Bernardini, Camilla, Mirabella, Massimiliano, Silvestri, Gabriella, Giglio, Vincenzo, Modoni, Anna, Pedemonte, Marina, Tasca, Giorgio, Galluzzi, Giuliana, Mercuri, Eugenio, Tonali, Pietro A, Ricci, Enzo

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Elevated serum Neurofilament Light chain (NfL) as a potential biomarker of neurological involvement in Myotonic Dystrophy type 1 (DM1) von Nicoletti, Tommaso F., Rossi, Salvatore, Vita, Maria Gabriella, Perna, Alessia, Guerrera, Gisella, Lino, Federica, Iacovelli, Chiara, Di Natale, Daniele, Modoni, Anna, Battistini, Luca, Silvestri, Gabriella

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A man with sarcoidosis and slurred speech von Nicoletti, T., Gaudino, S., Colacicco, G., Ausili Cefaro, L., Tasca, G., Guglielmi, V., Modoni, A., Gessi, M., Silvestri, G., Frisullo, G.

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High Prevalence and Gender-Related Differences of Gastrointestinal Manifestations in a Cohort of DM1 Patients: A Perspective, Cross-Sectional Study von Perna, Alessia, Maccora, Daria, Rossi, Salvatore, Nicoletti, Tommaso Filippo, Zocco, Maria Assunta, Riso, Vittorio, Modoni, Anna, Petrucci, Antonio, Valenza, Venanzio, Grieco, Antonio, Miele, Luca, 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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A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia von Hasan, Sonia, Bove, Cecilia, Silvestri, Gabriella, Mantuano, Elide, Modoni, Anna, Veneziano, Liana, Macchioni, Lara, Hunter, Therese, Hunter, Gary, Pessia, Mauro, D’Adamo, Maria Cristina

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Response to “Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype” von Rossi, Salvatore, Perna, Alessia, Modoni, Anna, Bertini, Enrico, Riso, Vittorio, Nicoletti, Tommaso Filippo, Silvestri, Gabriella

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Cognitive impairment in myotonic dystrophy type 1 (DM1) von Modoni, A, Silvestri, G, Vita, MGabriella, Quaranta, D, Tonali, P A, Marra, C

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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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Compound heterozygosity for an expanded (GAA) and a (GAAGGA) repeat at FXN locus: from a diagnostic pitfall to potential clues to the pathogenesis of Friedreich ataxia von Santoro, Massimo, Perna, Alessia, La Rosa, Piergiorgio, Petrillo, Sara, Piemonte, Fiorella, Rossi, Salvatore, Riso, Vittorio, Nicoletti, Tommaso Filippo, Modoni, Anna, Pomponi, Maria Grazia, Chiurazzi, Pietro, Silvestri, Gabriella

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Cognitive impairment in myotonic dystrophy type 1 (DM1): A longitudinal follow-up study von Modoni, A., Silvestri, G., Vita, M. Gabriella, Quaranta, D., Tonali, P. A., Marra, C.

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Resveratrol corrects aberrant splicing of RYR1 pre-mRNA and Ca2+ signal in myotonic dystrophy type 1 myotubes von Santoro, Massimo, Piacentini, Roberto, Perna, Alessia, Pisano, Eugenia, Severino, Anna, Modoni, Anna, Grassi, Claudio, Silvestri, Gabriella

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Alternative splicing alterations of Ca2+ handling genes are associated with Ca2+ signal dysregulation in myotonic dystrophy type 1 (DM1) and type 2 (DM2) myotubes von Santoro, Massimo, Piacentini, Roberto, Masciullo, Marcella, Bianchi, Maria Laura Ester, Modoni, Anna, Podda, Maria Vittoria, Ricci, Enzo, Silvestri, Gabriella, Grassi, Claudio

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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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Serial neuroimaging findings in a novel case of sporadic progressive ataxia and palatal tremor (PAPT) von Di Blasi, Chiara, Rizzo, Valentina, Di Lella, Giuseppe, Modoni, Anna, Calcagni, Maria Lucia, Picciotti, Pasqualina Maria, Silvestri, Gabriella

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Resveratrol corrects aberrant splicing of RYR1 pre-mRNA and Ca 2+ signal in myotonic dystrophy type 1 myotubes von Santoro, Massimo, Piacentini, Roberto, Perna, Alessia, Pisano, Eugenia, Severino, Anna, Modoni, Anna, Grassi, Claudio, Silvestri, Gabriella

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Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions von Santoro, Massimo, Masciullo, Marcella, Pietrobono, Roberta, Conte, Giulia, Modoni, Anna, Bianchi, Maria Laura E., Rizzo, Valentina, Pomponi, Maria Grazia, Tasca, Giorgio, Neri, Giovanni, Silvestri, Gabriella

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Substrate reduction therapy with miglustat in chronic GM2 gangliosidosis type Sandhoff: results of a 3-year follow-up von Masciullo, Marcella, Santoro, Massimo, Modoni, Anna, Ricci, Enzo, Guitton, Jerome, Tonali, Pietro, Silvestri, Gabriella

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Dysautonomia as Onset Symptom of Myotonic Dystrophy Type 2 von Rossi, Salvatore, Romano, Angela, Modoni, Anna, Perna, Francesco, Rizzo, Valentina, Santoro, Massimo, Monforte, Mauro, Pieroni, Maurizio, Luigetti, Marco, Pomponi, Maria Grazia, Silvestri, Gabriella

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