Alessandro Geroldi
6PUBLICATIONS
6CO-AUTHORS
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Publications (6)
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|Sep 09, 2024
Clinical and genetic features of CMT2T in Italian patients confirm the importance of MME pathogenic variants in idiopathic, late-onset axonal neuropathies.Alessandro Geroldi, Andrea La Barbera, Alessia Mammi
|Jun 14, 2024
The neurological core features of the infantile-onset multisystem neurologic, endocrine, and pancreatic disease: A novel nonsense mutation in an Italian family.Alessia Mammi, Alessandro Geroldi, Serena Patrone
|Jun 13, 2024
Next-generation sequencing in Charcot-Marie-Tooth: a proposal for improvement of ACMG guidelines for variant evaluation.Alessandro Geroldi, Alessia Mammi, Andrea Gaudio
|Oct 28, 2023
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers.Alessandro Geroldi, Stefano Tozza, Chiara Fiorillo
|Apr 12, 2020
Early onset demyelinating Charcot-Marie-Tooth disease caused by a novel in-frame isoleucine deletion in peripheral myelin protein 2.Alessandro Geroldi, Valeria Prada, Francesca Veneri
|Oct 06, 2018
Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise".Marina Grandis, Alessandro Geroldi, Rossella Gulli
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