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Annals of Clinical and Translational Neurology|February 6, 2021
Type I SMA "new natural history": long-term data in nusinersen-treated patientsMarika Pane, Giorgia Coratti, Valeria A Sansone, et al.Neuromuscular Disorders : NMD|June 8, 2021
Age related treatment effect in type II Spinal Muscular Atrophy pediatric patients treated with nusinersenGiorgia Coratti, Marika Pane, Simona Lucibello, et al.Neuromuscular Disorders : NMD|March 28, 2021
The nonsense mutation stop+4 model correlates with motor changes in Duchenne muscular dystrophyClaudia Brogna, Giorgia Coratti, Rachele Rossi, et al.Plos One|July 29, 2022
Age, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular DystrophyGiorgia Coratti, Jacopo Lenkowicz, Giulia Norcia, et al.BMC Neurology|February 25, 2017
Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophyMaria C Pera, Giorgia Coratti, Nicola Forcina, 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 Neurology|September 14, 2020
Clinical Variability in Spinal Muscular Atrophy Type IIIGiorgia Coratti, Sonia Messina, Simona Lucibello, et al.Pageof 4