Mattia Parisi

Publication Activity (10 Years)

Years Active: 2022-2022
Publications (10 Years): 5

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Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

European journal of neurology

This page only lists publications with an associated author ORCID identifier.

Publications

Mattia Parisi, Antonio Canosa, Alessandra Tessa, Bruno Ferrero, Salvatore Gallone
A patient with demyelinating CMT carrying the p.Y347C heterozygous variant of the MME gene and the p.L131F heterozygous variant of the HARS1 gene. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (2022)
Mattia Parisi, Antonio Canosa, Alessandra Tessa, Bruno Ferrero, Salvatore Gallone
A patient with demyelinating CMT carrying the p.Y347C heterozygous variant of the MME gene and the p.L131F heterozygous variant of the HARS1 gene. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 44 (4) (2022)
Mattia Parisi, Antonio Canosa, Alessandra Tessa, Bruno Ferrero, Salvatore Gallone
A patient with demyelinating CMT carrying the p.Y347C heterozygous variant of the MME gene and the p.L131F heterozygous variant of the HARS1 gene. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 44 (4) (2022)
Mattia Parisi, Irene Dogliotti, Michele Clerico, Davide Bertuzzo, Giulia Benevolo, Lorella Orsucci, Irene Schiavetti, Roberto Cavallo, Federica Cavallo, Simone Ragaini, Alessandra Di Liberto, Martina Ferrante, Giulia Bondielli, Carlo Alberto Artusi, Daniela Drandi, Leonardo Lopiano, Bruno Ferrero, Simone Ferrero
Efficacy of rituximab in anti-myelin-associated glycoprotein demyelinating polyneuropathy: Clinical, hematological and neurophysiological correlations during 2 years of follow-up. European journal of neurology 29 (12) (2022)
Mattia Parisi, Antonio Canosa, Alessandra Tessa, Bruno Ferrero, Salvatore Gallone
A patient with demyelinating CMT carrying the p.Y347C heterozygous variant of the MME gene and the p.L131F heterozygous variant of the HARS1 gene. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 44 (4) (2022)