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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 10, 2024
The use of digital tools in rare neurological diseases towards a new care model: a narrative reviewFrancesca Torri, Gabriele Vadi, Adriana Meli, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 25, 2022
Frailties and critical issues in neuromuscular diseases highlighted by SARS-CoV-2 pandemic: how many patients are still "invisible"?Giulia Ricci, Francesca Torri, Francesca Bianchi, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 4, 2025
Deciphering Facioscapulohumeral Dystrophy in the clinical trials era: where are we now?Francesca Torri, Beatrice Ciurli, Mariaconcetta Rende, et al.Journal of Neuromuscular Diseases|January 8, 2024
Characterization of Phenotypic Variability in Becker Muscular Dystrophy for Clinical Practice and Towards Trial Readiness: A Two-Years Follow up StudyGiulia Ricci, Alessandra Govoni, Francesca Torri, et al.Clinical and Experimental Rheumatology|February 24, 2023
The role of magnetic resonance imaging in the diagnostic work-out of myopathies: differential diagnosis between inflammatory myopathies and muscular dystrophiesSimone Barsotti, Giacomo Aringhieri, Barbara Mugellini, et al.Journal of Cardiovascular Medicine (Hagerstown, Md.)|May 2, 2023
Cardiac magnetic resonance findings and prognosis in type 1 myotonic dystrophyMarco Leali, Alberto Aimo, Giulia Ricci, et al.Clinical Genetics|August 11, 2025
The Role of Whole-Exome Sequencing and Methylation Analysis in Untangling Complex Facioscapulo-Humeral Muscular Dystrophy CasesFrancesca Torri, Claudia Strafella, Liliana Vercelli, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 12, 2025
Describing phenotypes in FSHD: an update of the comprehensive clinical evaluation formGiulia Ricci, Francesca Torri, Lucia Ruggiero, et al.Journal of Neuromuscular Diseases|April 25, 2022
A Single mtDNA Deletion in Association with a LMNA Gene New Frameshift Variant: A Case ReportVincenzo Montano, Michelangelo Mancuso, Costanza Simoncini, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|December 13, 2023
Proposal of a new clinical protocol for evaluating fatigability in adult SMA patientsGiulia Ricci, Francesca Torri, Alessandra Govoni, et al.Pageof 3