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Journal of Neurology|February 6, 2019
Six-minute walk test is reliable and sensitive in detecting response to therapy in CIDPEmanuele Spina, Antonietta Topa, Rosa Iodice, et al.Journal of Neurology|August 4, 2017
Early predictive factors of disability in CIDPEmanuele Spina, Antonietta Topa, Rosa Iodice, et al.Antioxidants (Basel, Switzerland)|November 27, 2024
Muscle Proteome Analysis of Facioscapulohumeral Dystrophy Patients Reveals a Metabolic Rewiring Promoting Oxidative/Reductive Stress Contributing to the Loss of Muscle FunctionManuela Moriggi, Lucia Ruggiero, Enrica Torretta, et al.Journal of the Peripheral Nervous System : JPNS|May 14, 2021
Proximal weakness involvement in the first Italian case of Charcot-Marie-Tooth 2CC harboring a novel frameshift variant in NEFHFrancesco Aruta, Daniele Severi, Aniello Iovino, et al.Journal of Neurology|February 27, 2014
Central cholinergic dysfunction in the adult form of Niemann Pick disease type C: a further link with Alzheimer's disease?Fiore Manganelli, Raffaele Dubbioso, Rosa Iodice, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 5, 2012
Electrophysiological comparison between males and females in HNPPFiore Manganelli, Chiara Pisciotta, Raffaele Dubbioso, et al.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.Frontiers in Immunology|April 4, 2022
Case Report: Severe Rhabdomyolysis and Multiorgan Failure After ChAdOx1 nCoV-19 VaccinationEmilia Cirillo, Ciro Esposito, Giuliana Giardino, 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.Pageof 8