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Neurology|October 17, 2020
Respiratory Trajectories in Type 2 and 3 Spinal Muscular Atrophy in the iSMAC Cohort StudyFederica Trucco, Deborah Ridout, Mariacristina Scoto, et al.Neuromuscular Disorders : NMD|January 4, 2022
Revised upper limb module in type II and III spinal muscular atrophy: 24-month changesGiorgia Coratti, Maria Carmela Pera, Jacqueline Montes, et al.European Journal of Neurology|June 27, 2025
Longitudinal Assessment of 4-Year HFMSE Changes in SMA II and III Patients Treated With NusinersenGiorgia Coratti, Francesca Bovis, Marika Pane, et al.Journal of Neuromuscular Diseases|March 1, 2024
Disease Trajectories in the Revised Hammersmith Scale in a Cohort of Untreated Patients with Spinal Muscular Atrophy types 2 and 3Amy Wolfe, Georgia Stimpson, Danielle Ramsey, et al.Muscle & Nerve|July 30, 2021
Different trajectories in upper limb and gross motor function in spinal muscular atrophyGiorgia Coratti, Maria Carmela Pera, Jacqueline Montes, et al.Plos One|June 21, 2018
Upper limb function in Duchenne muscular dystrophy: 24 month longitudinal dataMarika Pane, Giorgia Coratti, Claudia Brogna, et al.Journal of Neuromuscular Diseases|February 16, 2024
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient CardiomyopathyLuca Bello, Daniele Sabbatini, Aurora Fusto, et al.Annals of Clinical and Translational Neurology|April 29, 2020
Genetic modifiers of respiratory function in Duchenne muscular dystrophyLuca Bello, Grazia D'Angelo, Matteo Villa, et al.European Journal of Neurology|October 11, 2024
Long-term natural history in type II and III spinal muscular atrophy: a 4-year international study on the Hammersmith Functional Motor Scale ExpandedGiorgia Coratti, Francesca Bovis, Maria Carmela Pera, et al.Drugs in R&D|May 28, 2025
Opinion of the Italian Association of Myology on Ataluren for the Treatment of Nonsense Mutation Duchenne Muscular DystrophyLuca Bello, Pietro Riguzzi, Emilio Albamonte, et al.Pageof 7