It’s time to measure disability in spinal muscular atrophy
Antonio Trabacca, Camilla Ferrante, Marta De Rinaldis
DOI 10.36185/2532-1900-070
Fascicolo 2-2022
Letter to the Editor
Original article
The role of BAG3 in dilated cardiomyopathy and its association with Charcot-Marie-Tooth disease type 2
Nitya Yerabandi 1, Valentina L. Kouznetsova 2,3, Santosh Kesari 4, Igor F. Tsigelny 2-6
DOI 10.36185/2532-1900-071
Muscle quantitative MRI in adult SMA patients on nusinersen treatment: a longitudinal study
Annamaria Gallone 1, Federica Mazzi 2, Silvia Bonanno 1, Riccardo Zanin 3, Marco Moscatelli 2,4, Domenico Aquino 2, Lorenzo Maggi 1
DOI 10.36185/2532-1900-074
Peripheral circulation disturbances in two consecutive children with spinal muscular atrophy and literature review
Gloria Cristofano, Martina Fucci, Maria Carmela Oliva, Marta De Rinaldis, Antonio Trabacca
DOI 10.36185/2532-1900-072
Impact of the COVID-19 pandemic on neuromuscular rehabilitation setting. Part 2: patients and families’ views on the received health care during the pandemic
Lorenza Magliano 1, Giulia Citarelli 2, Maria Grazia Esposito 2, Vito Torre 2, Luisa Politano 2
DOI 10.36185/2532-1900-075
Case report
Autosomal dominant Ullrich congenital muscular dystrophy due to a de novo mutation in COL6A3 gene. A case report
Esther Picillo 1, Annalaura Torella 1,2, Luigia Passamano 1, Vincenzo Nigro 1,2,3, Luisa Politano 1
DOI 10.36185/2532-1900-073
NEWS FROM AROUND THE WORLD
NEWS FROM AROUND THE WORLD
FORTHCOMING MEETINGS
FORTHCOMING MEETINGS
