Assessment and management of respiratory function in patients with Duchenne muscular dystrophy: current and emerging options

por LoMauro, Antonella, D’Angelo, Maria Grazia, Aliverti, Andrea
Publicado 2015

Assessment of diaphragmatic thickness by ultrasonography in Duchenne muscular dystrophy (DMD) patients

por Laviola, Marianna, Priori, Rita, D’Angelo, Maria Grazia, Aliverti, Andrea
Publicado 2018

Non-Invasive Respiratory Assessment in Duchenne Muscular Dystrophy: From Clinical Research to Outcome Measures

por Pennati, Francesca, LoMauro, Antonella, D’Angelo, Maria Grazia, Aliverti, Andrea
Publicado 2021

A Wearable Device for Breathing Frequency Monitoring: A Pilot Study on Patients with Muscular Dystrophy

por Cesareo, Ambra, Nido, Santa Aurelia, Biffi, Emilia, Gandossini, Sandra, D’Angelo, Maria Grazia, Aliverti, Andrea
Publicado 2020

Is Social Training Delivered with a Head-Mounted Display Suitable for Patients with Hereditary Ataxia?

por Malerba, Giorgia, Bellazzecca, Silvia, Urgesi, Cosimo, Butti, Niccolò, D’Angelo, Maria Grazia, Diella, Eleonora, Biffi, Emilia
Publicado 2023

Rib Cage Deformities Alter Respiratory Muscle Action and Chest Wall Function in Patients with Severe Osteogenesis Imperfecta

por LoMauro, Antonella, Pochintesta, Simona, Romei, Marianna, D'Angelo, Maria Grazia, Pedotti, Antonio, Turconi, Anna Carla, Aliverti, Andrea
Publicado 2012

Psychological and practical difficulties among parents and healthy siblings of children with Duchenne vs. Becker muscular dystrophy: an Italian comparative study

por MAGLIANO, LORENZA, D'ANGELO, MARIA GRAZIA, VITA, GIUSEPPE, PANE, MARIKA, D'AMICO, ADELE, BALOTTIN, UMBERTO, ANGELINI, CORRADO, BATTINI, ROBERTA, POLITANO, LUISA
Publicado 2014

User-centred assistive SystEm for arm Functions in neUromuscuLar subjects (USEFUL): a randomized controlled study

por Longatelli, Valeria, Antonietti, Alberto, Biffi, Emilia, Diella, Eleonora, D’Angelo, Maria Grazia, Rossini, Mauro, Molteni, Franco, Bocciolone, Marco, Pedrocchi, Alessandra, Gandolla, Marta
Publicado 2021

Case Reports: Novel Missense Variants in the Filamin C Actin Binding Domain Cause Variable Phenotypes

por Velardo, Daniele, D'Angelo, Maria Grazia, Citterio, Andrea, Panzeri, Elena, Napoli, Laura, Cinnante, Claudia, Moggio, Maurizio, Comi, Giacomo Pietro, Ronchi, Dario, Bassi, Maria Teresa
Publicado 2022

Correlation of Circulating CD133+ Progenitor Subclasses with a Mild Phenotype in Duchenne Muscular Dystrophy Patients

por Marchesi, Chiara, Belicchi, Marzia, Meregalli, Mirella, Farini, Andrea, Cattaneo, Alessandra, Parolini, Daniele, Gavina, Manuela, Porretti, Laura, D'Angelo, Maria Grazia, Bresolin, Nereo, Cossu, Giulio, Torrente, Yvan
Publicado 2008

Neurocognitive Profiles in Duchenne Muscular Dystrophy and Gene Mutation Site

por D’Angelo, Maria Grazia, Lorusso, Maria Luisa, Civati, Federica, Comi, Giacomo Pietro, Magri, Francesca, Del Bo, Roberto, Guglieri, Michela, Molteni, Massimo, Turconi, Anna Carla, Bresolin, Nereo
Publicado 2011

Functional and Structural Brain Damage in Friedreich's Ataxia

por Vavla, Marinela, Arrigoni, Filippo, Nordio, Andrea, De Luca, Alberto, Pizzighello, Silvia, Petacchi, Elisa, Paparella, Gabriella, D'Angelo, Maria Grazia, Brighina, Erika, Russo, Emanuela, Fantin, Marianna, Colombo, Paola, Martinuzzi, Andrea
Publicado 2018

ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases

por Magri, Francesca, Colombo, Irene, Del Bo, Roberto, Previtali, Stefano, Brusa, Roberta, Ciscato, Patrizia, Scarlato, Marina, Ronchi, Dario, D’Angelo, Maria Grazia, Corti, Stefania, Moggio, Maurizio, Bresolin, Nereo, Comi, Giacomo Pietro
Publicado 2015

Sensitivity of Neuroimaging Indicators in Monitoring the Effects of Interferon Gamma Treatment in Friedreich’s Ataxia

por Vavla, Marinela, Arrigoni, Filippo, Toschi, Nicola, Peruzzo, Denis, D’Angelo, Maria Grazia, Gandossini, Sandra, Russo, Annamaria, Diella, Eleonora, Tirelli, Stefania, Salati, Roberto, Rufini, Alessandra, Condo, Ivano, Testi, Roberto, Martinuzzi, Andrea
Publicado 2020

Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome)

por Kurtas, Nehir, Arrigoni, Filippo, Errichiello, Edoardo, Zucca, Claudio, Maghini, Cristina, D’Angelo, Maria Grazia, Beri, Silvana, Giorda, Roberto, Bertuzzo, Sara, Delledonne, Massimo, Xumerle, Luciano, Rossato, Marzia, Zuffardi, Orsetta, Bonaglia, Maria Clara
Publicado 2018

Clinical and genetic features of a cohort of patients with MFN2-related neuropathy

por Abati, Elena, Manini, Arianna, Velardo, Daniele, Del Bo, Roberto, Napoli, Laura, Rizzo, Federica, Moggio, Maurizio, Bresolin, Nereo, Bellone, Emilia, Bassi, Maria Teresa, D’Angelo, Maria Grazia, Comi, Giacomo Pietro, Corti, Stefania
Publicado 2022

Intraarterial Injection of Muscle-Derived Cd34(+)Sca-1(+) Stem Cells Restores Dystrophin in mdx Mice

por Torrente, Yuan, Tremblay, Jacques-P, Pisati, Federica, Belicchi, Marzia, Rossi, Barbara, Sironi, Manuela, Fortunato, Franco, El Fahime, Mostafa, D'Angelo, Maria Grazia, Caron, Nicolas J., Constantin, Gabriela, Paulin, Denise, Scarlato, Guglielmo, Bresolin, Nereo
Publicado 2001

Extracellular Matrix Disorganization and Sarcolemmal Alterations in COL6-Related Myopathy Patients with New Variants of COL6 Genes

por Zanotti, Simona, Magri, Francesca, Salani, Sabrina, Napoli, Laura, Ripolone, Michela, Ronchi, Dario, Fortunato, Francesco, Ciscato, Patrizia, Velardo, Daniele, D’Angelo, Maria Grazia, Gualandi, Francesca, Nigro, Vincenzo, Sciacco, Monica, Corti, Stefania, Comi, Giacomo Pietro, Piga, Daniela
Publicado 2023

Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients

por Magri, Francesca, Bo, Roberto Del, D’Angelo, Maria Grazia, Sciacco, Monica, Gandossini, Sandra, Govoni, Alessandra, Napoli, Laura, Ciscato, Patrizia, Fortunato, Francesco, Brighina, Erika, Bonato, Sara, Bordoni, Andreina, Lucchini, Valeria, Corti, Stefania, Moggio, Maurizio, Bresolin, Nereo, Comi, Giacomo Pietro
Publicado 2012

Treatment effect of idebenone on inspiratory function in patients with Duchenne muscular dystrophy

por Buyse, Gunnar M., Voit, Thomas, Schara, Ulrike, Straathof, Chiara S.M., D'Angelo, Maria Grazia, Bernert, Günther, Cuisset, Jean‐Marie, Finkel, Richard S., Goemans, Nathalie, Rummey, Christian, Leinonen, Mika, Mayer, Oscar H., Spagnolo, Paolo, Meier, Thomas, McDonald, Craig M.
Publicado 2016