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Therapeutic Advances in Neurological Disorders|December 14, 2018
One-year follow up of three Italian patients with Duchenne muscular dystrophy treated with ataluren: is earlier better?Lucia Ruggiero, Rosa Iodice, Marcello Esposito, et al.Neuropediatrics|December 1, 2021
Spinal Nerve Roots Abnormalities on MRI in a Child with SURF1 Mitochondrial DiseaseAlfonso Rubino, Giorgia Bruno, Federica Mazio, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 30, 2010
Electrophysiological characterisation in hereditary spastic paraplegia type 5Fiore Manganelli, Chiara Pisciotta, Raffaele Dubbioso, et al.Biomedicines|November 11, 2022
Quantitative Sensory Testing in Late-Onset ATTRv Presymptomatic Subjects: A Single Center ExperienceStefano Tozza, Daniele Severi, Giovanni Palumbo, et al.Multiple Sclerosis and Related Disorders|April 3, 2021
Alemtuzumab in Covid eraAniello Iovino, Nunzio Olivieri, Francesco Aruta, et al.Journal of the Neurological Sciences|December 25, 2014
Electrophysiological characterization of adult-onset Niemann-Pick type C diseaseRosa Iodice, Raffaele Dubbioso, Antonietta Topa, et al.Biomed Research International|June 6, 2019
RYR1 Sequence Variants in Myopathies: Expression and Functional Studies in Two FamiliesAlberto Zullo, Giuseppa Perrotta, Rossana D'Angelo, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|December 13, 2023
Pregnancy experience in women with spinal muscular atrophy: a case seriesRoberta Piera Bencivenga, Dario Zoppi, Anna Russo, et al.Archives of Neurology|April 13, 2011
Autoimmune autonomic ganglionopathy: a possible postganglionic neuropathyFiore Manganelli, Raffaele Dubbioso, Maria Nolano, et al.Journal of the Peripheral Nervous System : JPNS|May 7, 2021
The neuropathy in hereditary transthyretin amyloidosis: A narrative reviewStefano Tozza, Daniele Severi, Emanuele Spina, et al.Pageof 8