Mattia Parisi
2PUBLICATIONS
1CO-AUTHORS
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Publications (2)
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|Dec 14, 2022
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.Mattia Parisi, Antonio Canosa, Alessandra Tessa
|Sep 09, 2022
Efficacy of rituximab in anti-myelin-associated glycoprotein demyelinating polyneuropathy: Clinical, hematological and neurophysiological correlations during 2 years of follow-up.Mattia Parisi, Irene Dogliotti, Michele Clerico
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