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Journal of Neuromuscular Diseases|April 17, 2023
Longitudinal Analysis of PUL 2.0 Domains in Ambulant and Non-Ambulant Duchenne Muscular Dystrophy Patients: How do they Change in Relation to Functional Ability?Marika Pane, Giorgia Coratti, Claudia Brogna, et al.
Annals of Clinical and Translational Neurology|March 19, 2026
Onasemnogene Abeparvovec in Type I Spinal Muscular Atrophy: 24-Month Follow-Up From the Italian RegistryMarika Pane, Giorgia Coratti, Chiara Cutrì, et al.
Neurology. Clinical Practice|June 27, 2024
Therapeutic Role of Nusinersen on Respiratory Progression in Pediatric Patients With Spinal Muscular Atrophy Type 2 and Nonambulant Type 3Federica Trucco, Deborah Ridout, Harriet Weststrate, et al.
Epilepsia|October 21, 2016
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective multicentre studyMarilena Vecchi, Carmen Barba, Debora De Carlo, et al.
Neuromuscular Disorders : NMD|December 29, 2023
Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month studyGiorgia Coratti, Marika Pane, Claudia Brogna, et al.
European Journal of Pediatrics|December 16, 2024
Prevalence of Duchenne muscular dystrophy in Italy: a nationwide surveyAnna Capasso, Gianpaolo Cicala, Martina Ricci, et al.
Annals of Neurology|September 14, 2020
Clinical Variability in Spinal Muscular Atrophy Type IIIGiorgia Coratti, Sonia Messina, Simona Lucibello, et al.
Brain : a Journal of Neurology|November 5, 2024
Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severityDomenico Gorgoglione, Daniele Sabbatini, Pietro Riguzzi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|September 9, 2020
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phaseEleonora Mauri, Elena Abati, Olimpia Musumeci, et al.
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