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Archives of Disease in Childhood|May 16, 2022
Oral and Swallowing Abilities Tool (OrSAT) in nusinersen treated patientsBeatrice Berti, Lavinia Fanelli, Giulia Stanca, et al.International Journal of Molecular Sciences|July 27, 2024
De Novo DNM1L Mutation in a Patient with Encephalopathy, Cardiomyopathy and Fatal Non-Epileptic Paroxysmal Refractory VomitingBeatrice Berti, Daniela Verrigni, Alessia Nasca, et al.Plos One|March 24, 2020
Diagnostic journey in Spinal Muscular Atrophy: Is it still an odyssey?Maria Carmela Pera, Giorgia Coratti, Beatrice Berti, et al.Children (Basel, Switzerland)|June 26, 2026
Oral and Swallowing Abilities Tool (OrSAT) in Individuals with Type I SMA Older than 24 Months: A Pilot StudyGiulia Stanca, Maria Sframeli, Camilla Verdilio, et al.Neuromuscular Disorders : NMD|August 23, 2023
Patient reported outcome measure for upper limb in Duchenne muscular dystrophy: correlation with PUL2.0Gianpaolo Cicala, Marika Pane, Giorgia Coratti, et al.Dysphagia|June 8, 2023
Assessing Prevalence and Characteristics of Oro-bulbar Involvement in Children and Adults with SMA Type 2 and 3 Using a Multimodal ApproachFederica Trucco, Francesca Salmin, Andrea Lizio, et al.European Journal of Pediatrics|May 6, 2022
Neurological assessment of newborns with spinal muscular atrophy identified through neonatal screeningMarika Pane, Maria Alice Donati, Costanza Cutrona, et al.Annals of Neurology|June 23, 2019
Nusinersen in type 1 spinal muscular atrophy: Twelve-month real-world dataMarika Pane, Giorgia Coratti, Valeria A Sansone, et al.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.European Journal of Pediatrics|January 20, 2022
Body mass index in type 2 spinal muscular atrophy: a longitudinal studyGloria Ferrantini, Giorgia Coratti, Roberta Onesimo, et al.Pageof 5