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Frontiers in Neurology|March 15, 2024
The impact of three <i>SMN2</i> gene copies on clinical characteristics and effect of disease-modifying treatment in patients with spinal muscular atrophy: a systematic literature reviewClaudia Dosi, Riccardo Masson
Developmental Medicine and Child Neurology|September 6, 2017
Efficacy of oral pharmacological treatments in dyskinetic cerebral palsy: a systematic reviewRiccardo Masson, Emanuela Pagliano, Giovanni Baranello
Developmental Medicine and Child Neurology|January 16, 2021
Brain, cognition, and language development in spinal muscular atrophy type 1: a scoping reviewRiccardo Masson, Chiara Brusa, Mariacristina Scoto, et al.
International Journal of Neonatal Screening|November 24, 2025
Treating Presymptomatic Spinal Muscular Atrophy Patients with Onasemnogene Abeparvovec in Italy: The Role of the National Health System and Drug Supply. Comment on Zaidman et al. Newborn Screening for Spinal Muscular Atrophy: Variations in Practice and Early Management of Infants with Spinal Muscular Atrophy in the United States. <i>Int. J. Neonatal Screen.</i> 2024, <i>10</i>, 58Riccardo Masson, Serena Gaballo, Raffaella Caravita, et al.
Molecular Genetics & Genomic Medicine|December 4, 2020
Expanding the PURA syndrome phenotype: A child with the recurrent PURA p.(Phe233del) pathogenic variant showing similarities with cutis laxaValeria Cinquina, Claudia Ciaccio, Marina Venturini, et al.
Child Neurology Open|February 23, 2019
A Not So Benign Family Pedigree With Hereditary Chorea: A Broader Phenotypic Expression or Additional Picture?Roberta Milone, Riccardo Masson, Caterina Di Cosmo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 18, 2020
Motor learning in unilateral cerebral palsy and the influence of corticospinal tract reorganizationMaíra I S Carneiro, Cristina Russo, Riccardo Masson, et al.
Audiology Research|October 28, 2025
Exploring the Trajectory of Swallowing Within Psychomotor Development in Spinal Muscular Atrophy: Moving Toward Integrated CareSofia Gandolfi, Claudia Dosi, Stefano Parravicini, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 25, 2018
Outcome measures for children with movement disordersEmanuela Pagliano, Giovanni Baranello, Riccardo Masson, et al.
Neuromuscular Disorders : NMD|July 4, 2019
Evolution of bone mineral density, bone metabolism and fragility fractures in Spinal Muscular Atrophy (SMA) types 2 and 3Giovanni Baranello, Silvia Vai, Francesca Broggi, et al.
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