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Archives of Disease in Childhood|January 30, 2024
Communicative development inventory in type 1 and presymptomatic infants with spinal muscular atrophy: a cohort studyBianca Buchignani, Gianpaolo Cicala, Francesca Cumbo, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 28, 2025
Patients on treatment with risdiplam in Italy: challenges in the interpretation of the real-world dataEmilio Albamonte, Adrea Lizio, Giorgia Coratti, et al.
Annals of Clinical and Translational Neurology|August 20, 2025
Long-Term Evaluation of Givinostat in Duchenne Muscular Dystrophy, and Natural History ComparisonsCraig M McDonald, Michela Guglieri, Dragana Vučinić, et al.
Eclinicalmedicine|December 17, 2024
Type I spinal muscular atrophy and disease modifying treatments: a nationwide study in children born since 2016Maria Carmela Pera, Giorgia Coratti, Marika Pane, et al.
Journal of Neuromuscular Diseases|September 18, 2025
Upper limb progression in Duchenne muscular dystrophy: Insights from a 36-month longitudinal study using the PUL 20Giorgia Coratti, Marika Pane, Sophia Paolucci, et al.
European Journal of Neurology|March 7, 2023
Type I spinal muscular atrophy patients treated with nusinersen: 4-year follow-up of motor, respiratory and bulbar functionMarika Pane, Giorgia Coratti, Valeria A Sansone, et al.
Journal of Neurology|May 5, 2022
Genetic modifiers of upper limb function in Duchenne muscular dystrophyDaniele Sabbatini, Aurora Fusto, Sara Vianello, et al.
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