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Muscle & Nerve|September 27, 2014
Muscle fiber type disproportion (FTD) in a family with mutations in the LMNA geneLucia Ruggiero, Chiara Fiorillo, Alessandra Tessa, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 15, 2018
Long-term therapy with miglustat and cognitive decline in the adult form of Niemann-Pick disease type C: a case reportStefano Tozza, Raffaele Dubbioso, Rosa Iodice, et al.Biochemical and Biophysical Research Communications|January 11, 2015
A rare mutation in MYH7 gene occurs with overlapping phenotypeLucia Ruggiero, Chiara Fiorillo, Sara Gibertini, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 26, 2021
The impact of symptoms on daily life as perceived by patients with Charcot-Marie-Tooth type 1A diseaseStefano Tozza, Dario Bruzzese, Daniele Severi, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 2, 2024
Charcot-Marie-Tooth type 2CC misdiagnosed as Chronic Inflammatory Demyelinating PolyradiculoneuropathyIsabella Di Sarno, Stefano Tozza, Filippo Maria Santorelli, et al.Annals of Clinical and Translational Neurology|October 21, 2020
Multimodal evaluation of an Italian family with a hereditary spastic paraplegia and POLR3A mutationsLucia Ruggiero, Aniello Iovino, Raffaele Dubbioso, et al.Restorative Neurology and Neuroscience|October 7, 2017
The therapeutic use of non-invasive brain stimulation in multiple sclerosis - a reviewRosa Iodice, Fiore Manganelli, Raffaele DubbiosoJournal of Neurophysiology|December 22, 2021
BDNF polymorphism and interhemispheric balance of motor cortex excitability: a preliminary studyRaffaele Dubbioso, Giovanni Pellegrino, Federico Ranieri, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 23, 2023
Heterogenous electrophysiological features in early stage of hereditary transthyretin amyloidosis neuropathyStefano Tozza, Giovanni Palumbo, Daniele Severi, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 28, 2019
Different cortical excitability profiles in hereditary brain iron and copper accumulationRaffaele Dubbioso, Lucia Ruggiero, Marcello Esposito, et al.Pageof 28