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Alessandro Geroldi

6PUBLICATIONS

6CO-AUTHORS

Medical mycologyNeonatologyGene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesMedical infection agents (incl. prions)

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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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Frequent Collaborators

2 joint publications

Stefano Tozza

2 joint publications

Lucio Marinelli

2 joint publications

Alessia Mammi

1 joint publications

Valeria Prada

1 joint publications

Paola Mandich

1 joint publications

Giulia Bisogni

Frequent Collaborators

2 joint publications

Stefano Tozza

2 joint publications

Lucio Marinelli

2 joint publications

Alessia Mammi

1 joint publications

Valeria Prada

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