Physiological aspects of muscular adaptations to training translated to neuromuscular diseases

por BERARDINELLI, ANGELA, D’ANTONA, GIUSEPPE
Publicado 2019

Good response to the late treatment with ataluren in a boy with Duchenne muscular dystrophy: could the previous mild course of the disease have affected the outcome?

por Pasca, Ludovica, Gardani, Alice, Paoletti, Matteo, Velardo, Daniele, Berardinelli, Angela
Publicado 2022

Growth Hormone Deficiency in a Patient with Becker Muscular Dystrophy: A Pediatric Case Report

por Calcaterra, Valeria, Malvezzi, Annachiara, Toglia, Rossana, Berardinelli, Angela, Bozzola, Elena, Bozzola, Mauro, Larizza, Daniela
Publicado 2013

Subcutaneous Immunoglobulin in Infantile Chronic Inflammatory Demyelinating Polyneuropathy: A Case Report

por Cianci, Paola, Salvatore, Silvia, Moretti, Alex, Berardinelli, Angela, Salvatoni, Alessandro, Marinoni, Maddalena, Agosti, Massimo
Publicado 2019

Advances in Quantitative Imaging of Genetic and Acquired Myopathies: Clinical Applications and Perspectives

por Paoletti, Matteo, Pichiecchio, Anna, Cotti Piccinelli, Stefano, Tasca, Giorgio, Berardinelli, Angela L., Padovani, Alessandro, Filosto, Massimiliano
Publicado 2019

An integrated approach in a case of facioscapulohumeral dystrophy

por Pasotti, Stefano, Magnani, Bruno, Longa, Emanuela, Giovanetti, Giuseppe, Rossi, Albino, Berardinelli, Angela, Tupler, Rossella, D’Antona, Giuseppe
Publicado 2014

Nutrition and Exercise in a Case of Carnitine Palmitoyl-Transferase II Deficiency

por Parimbelli, Mauro, Pezzotti, Elena, Negro, Massimo, Calanni, Luca, Allemano, Silvia, Bernardi, Marco, Berardinelli, Angela, D’Antona, Giuseppe
Publicado 2021

Exercise, Nutrition, and Supplements in the Muscle Carnitine Palmitoyl-Transferase II Deficiency: New Theoretical Bases for Potential Applications

por Negro, Massimo, Cerullo, Giuseppe, Parimbelli, Mauro, Ravazzani, Alberto, Feletti, Fausto, Berardinelli, Angela, Cena, Hellas, D’Antona, Giuseppe
Publicado 2021

Early Neurodevelopmental Findings Predict School Age Cognitive Abilities in Duchenne Muscular Dystrophy: A Longitudinal Study

por Chieffo, Daniela, Brogna, Claudia, Berardinelli, Angela, D’Angelo, Grazia, Mallardi, Maria, D’Amico, Adele, Alfieri, Paolo, Mercuri, Eugenio, Pane, Marika
Publicado 2015

Muscle Fiber Conduction Velocity Correlates With the Age at Onset in Mild FSHD Cases

por Beretta-Piccoli, Matteo, Negro, Massimo, Calanni, Luca, Berardinelli, Angela, Siciliano, Gabriele, Tupler, Rossella, Soldini, Emiliano, Cescon, Corrado, D’Antona, Giuseppe
Publicado 2021

Increased resistance towards fatigability in patients with facioscapulohumeral muscular dystrophy

por Beretta-Piccoli, Matteo, Calanni, Luca, Negro, Massimo, Ricci, Giulia, Bettio, Cinzia, Barbero, Marco, Berardinelli, Angela, Siciliano, Gabriele, Tupler, Rossella, Soldini, Emiliano, Cescon, Corrado, D’Antona, Giuseppe
Publicado 2021

Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G > A mitochondrial DNA mutation: a case report

por Ronchi, Dario, Cosi, Alessandra, Tonduti, Davide, Orcesi, Simona, Bordoni, Andreina, Fortunato, Francesco, Rizzuti, Mafalda, Sciacco, Monica, Collotta, Martina, Cagdas, Sophie, Capovilla, Giuseppe, Moggio, Maurizio, Berardinelli, Angela, Veggiotti, Pierangelo, Comi, Giacomo P
Publicado 2011

Centronuclear myopathy related to dynamin 2 mutations: Clinical, morphological, muscle imaging and genetic features of an Italian cohort

por Catteruccia, Michela, Fattori, Fabiana, Codemo, Valentina, Ruggiero, Lucia, Maggi, Lorenzo, Tasca, Giorgio, Fiorillo, Chiara, Pane, Marika, Berardinelli, Angela, Verardo, Margherita, Bragato, Cinzia, Mora, Marina, Morandi, Lucia, Bruno, Claudio, Santoro, Lucio, Pegoraro, Elena, Mercuri, Eugenio, Bertini, Enrico, D’Amico, Adele
Publicado 2013

Pilot Study on Quantitative Cervical Cord and Muscular MRI in Spinal Muscular Atrophy: Promising Biomarkers of Disease Evolution and Treatment?

por Savini, Giovanni, Asteggiano, Carlo, Paoletti, Matteo, Parravicini, Stefano, Pezzotti, Elena, Solazzo, Francesca, Muzic, Shaun I., Santini, Francesco, Deligianni, Xeni, Gardani, Alice, Germani, Giancarlo, Farina, Lisa M., Bergsland, Niels, Gandini Wheeler-Kingshott, Claudia A. M., Berardinelli, Angela, Bastianello, Stefano, Pichiecchio, Anna
Publicado 2021

Upper Limb Changes in DMD Patients Amenable to Skipping Exons 44, 45, 51 and 53: A 24-Month Study

por Brogna, Claudia, Pane, Marika, Coratti, Giorgia, D’Amico, Adele, Pegoraro, Elena, Bello, Luca, Sansone, Valeria Ada Maria, Albamonte, Emilio, Messina, Sonia, Pini, Antonella, D’Angelo, Maria Grazia, Bruno, Claudio, Mongini, Tiziana, Ricci, Federica Silvia, Berardinelli, Angela, Battini, Roberta, Masson, Riccardo, Bertini, Enrico Silvio, Politano, Luisa, Mercuri, Eugenio
Publicado 2023

Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy

por Ruggiero, Lucia, Mele, Fabiano, Manganelli, Fiore, Bruzzese, Dario, Ricci, Giulia, Vercelli, Liliana, Govi, Monica, Vallarola, Antonio, Tripodi, Silvia, Villa, Luisa, Di Muzio, Antonio, Scarlato, Marina, Bucci, Elisabetta, Antonini, Giovanni, Maggi, Lorenzo, Rodolico, Carmelo, Tomelleri, Giuliano, Filosto, Massimiliano, Previtali, Stefano, Angelini, Corrado, Berardinelli, Angela, Pegoraro, Elena, Moggio, Maurizio, Mongini, Tiziana, Siciliano, Gabriele, Santoro, Lucio, Tupler, Rossella
Publicado 2020

A 5-year clinical follow-up study from the Italian National Registry for FSHD

por Vercelli, Liliana, Mele, Fabiano, Ruggiero, Lucia, Sera, Francesco, Tripodi, Silvia, Ricci, Giulia, Vallarola, Antonio, Villa, Luisa, Govi, Monica, Maranda, Louise, Di Muzio, Antonio, Scarlato, Marina, Bucci, Elisabetta, Maggi, Lorenzo, Rodolico, Carmelo, Moggio, Maurizio, Filosto, Massimiliano, Antonini, Giovanni, Previtali, Stefano, Angelini, Corrado, Berardinelli, Angela, Pegoraro, Elena, Siciliano, Gabriele, Tomelleri, Giuliano, Santoro, Lucio, Mongini, Tiziana, Tupler, Rossella
Publicado 2020

Health-related quality of life and functional changes in DMD: A 12-month longitudinal cohort study

por Messina, Sonia, Vita, Gian Luca, Sframeli, Maria, Mondello, Stefania, Mazzone, Elena, D'Amico, Adele, Berardinelli, Angela, La Rosa, Matteo, Bruno, Claudio, Distefano, Maria Grazia, Baranello, Giovanni, Barcellona, Costanza, Scutifero, Marianna, Marcato, Sonia, Palmieri, Arianna, Politano, Luisa, Morandi, Lucia, Mongini, Tiziana, Pegoraro, Elena, D'Angelo, Maria Grazia, Pane, Marika, Rodolico, Carmelo, Minetti, Carlo, Bertini, Enrico, Vita, Giuseppe, Mercuri, Eugenio
Publicado 2016

Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53

por Brogna, Claudia, Coratti, Giorgia, Pane, Marika, Ricotti, Valeria, Messina, Sonia, D’Amico, Adele, Bruno, Claudio, Vita, Gianluca, Berardinelli, Angela, Mazzone, Elena, Magri, Francesca, Ricci, Federica, Mongini, Tiziana, Battini, Roberta, Bello, Luca, Pegoraro, Elena, Baranello, Giovanni, Previtali, Stefano C., Politano, Luisa, Comi, Giacomo P., Sansone, Valeria A., Donati, Alice, Bertini, Enrico, Muntoni, Francesco, Goemans, Nathalie, Mercuri, Eugenio
Publicado 2019

Correction: Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53

por Brogna, Claudia, Coratt, Giorgia, Pane, Marika, Ricotti, Valeria, Messina, Sonia, D’Amico, Adele, Bruno, Claudio, Vita, Gianluca, Berardinelli, Angela, Mazzone, Elena, Magri, Francesca, Ricci, Federica, Mongini, Tiziana, Battini, Roberta, Bello, Luca, Pegoraro, Elena, Baranello, Giovanni, Previtali, Stefano C., Politano, Luisa, Comi, Giacomo P., Sansone, Valeria A., Donati, Alice, Bertini, Enrico, Muntoni, Francesco, Goemans, Nathalie, Mercuri, Eugenio
Publicado 2019