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Neuromuscular Disorders : NMD|July 2, 2018
Nusinersen in type 1 SMA infants, children and young adults: Preliminary results on motor functionMarika Pane, Concetta Palermo, Sonia Messina, et al.
Cellular and Molecular Life Sciences : CMLS|September 10, 2024
Proteomics profiling and machine learning in nusinersen-treated patients with spinal muscular atrophyChiara Panicucci, Eray Sahin, Martina Bartolucci, et al.
Annals of Clinical and Translational Neurology|April 17, 2026
Safety and Tolerability of Givinostat: Evidence From Real-World and Clinical PracticeMarika Pane, Anna Capasso, Chiara Arpaia, et al.
European Journal of Medical Genetics|March 22, 2023
TeleNEwCARe: An Italian case-control telegenetics study in patients with Hereditary NEuromuscular and CARdiac diseasesMarianna Farnè, Fernanda Fortunato, Marcella Neri, et al.
Plos One|August 6, 2016
Revised North Star Ambulatory Assessment for Young Boys with Duchenne Muscular DystrophyEugenio Mercuri, Giorgia Coratti, Sonia Messina, 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.
Sleep Medicine|February 21, 2017
Sleep disorders in spinal muscular atrophyMaria C Pera, Domenico M Romeo, Alessandra Graziano, et al.
Neuromuscular Disorders : NMD|March 28, 2021
The Spinal Muscular Atrophy Health Index: Italian validation of a disease-specific outcome measureValeria A Sansone, Alice Pirola, Andrea Lizio, et al.
Journal of Neurology|November 29, 2019
MRI patterns of muscle involvement in type 2 and 3 spinal muscular atrophy patientsClaudia Brogna, Lara Cristiano, Tommaso Verdolotti, 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.
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