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Cells|May 14, 2020
Creatine Kinase and Progression Rate in Amyotrophic Lateral SclerosisMarco Ceccanti, Valeria Pozzilli, Chiara Cambieri, et al.Frontiers in Neurology|December 15, 2016
Laryngeal Sensitivity in Patients with Amyotrophic Lateral SclerosisGiovanni Ruoppolo, Emanuela Onesti, Maria Cristina Gori, et al.European Journal of Neurology|November 5, 2025
Polyneuropathy in Wild-Type Transthyretin AmyloidosisMaria Ausilia Sciarrone, Francesca Vitali, Valeria Guglielmino, et al.Brain, Behavior, and Immunity|December 13, 2024
GDF15-GFRAL signaling drives weight loss and lipid metabolism in mouse model of amyotrophic lateral sclerosisGermana Cocozza, Ludovica Maria Busdraghi, Giuseppina Chece, et al.Scientific Reports|February 28, 2019
Neuromuscular magnetic stimulation counteracts muscle decline in ALS patients: results of a randomized, double-blind, controlled studyAntonio Musarò, Gabriella Dobrowolny, Chiara Cambieri, et al.Antioxidants (Basel, Switzerland)|August 29, 2024
Oxidative Stress in Transthyretin-Mediated Amyloidosis: An Exploratory StudyMarco Fiore, Chiara Cambieri, Laura Libonati, et al.Inflammation and Regeneration|March 9, 2023
Immune-mediated myogenesis and acetylcholine receptor clustering promote a slow disease progression in ALS mouse modelsCassandra Margotta, Paola Fabbrizio, Marco Ceccanti, et al.Current Gene Therapy|February 24, 2026
Padlock Assay in Transthyretin Amyloidosis: A Feasibility StudyMaria Grazia Di Certo, Francesca Gabanella, Claudio Passananti, et al.Journal of the Neurological Sciences|March 15, 2024
Chronic inflammatory demyelinating polyneuropathy and HEV antibody status: A case-control study from Lazio, ItalyFederica Moret, Enea Spada, Marco Ceccanti, et al.Diagnostics (Basel, Switzerland)|February 26, 2025
Exploring Cardiac Sympathetic Denervation in Transthyretin-Mediated Hereditary Amyloidosis (ATTRv): Insights from <sup>123</sup>I-mIBG ScintigraphyMaria Silvia De Feo, Chiara Cambieri, Eleonora Galosi, et al.Pageof 4