Deconstructing speech alterations in episodic ataxia type 2: Perceptual-acoustic analysis in a case due to CACNA1A gene mutation.

Giacomo Argenziano, Francesco Cavallieri, Edoardo Monfrini, Annalisa Gessani, Marco Russo, Romana Rizzi, Valentina Fioravanti, Sara Grisanti, Giulia Toschi, Manuela Napoli, Rosario Pascarella, Carla Budriesi, Alessio Di Fonzo, Riccardo Zucco, Franco Valzania

Journal: Parkinsonism & related disorders 2023;108():105311

PMID: 36805178

Full Text on Elsevier Science View on PubMed

Abstract

Address: Neurology Unit, Neuromotor & Rehabilitation Department, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy; Neurology Unit, Department of Biomedical, Metabolic and Neural Science, University of Modena and Reggio Emilia, Modena, Italy.; Neurology Unit, Neuromotor & Rehabilitation Department, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy. Electronic address: [email protected].; Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Neurology Unit, Milan, Italy.; Neurology Unit, Department of Biomedical, Metabolic and Neural Science, University of Modena and Reggio Emilia, Modena, Italy.; Neurology Unit, Neuromotor & Rehabilitation Department, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.; Clinical and Experimental Medicine PhD Program, University of Modena and Reggio Emilia, Reggio Emilia, Italy.; Neuroradiology Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.

DOI: 10.1016/j.parkreldis.2023.105311

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MeSH Terms: Humans, Ataxia, Calcium Channels, Mutation, Nystagmus, Pathologic, Pedigree, Speech