Alessandro Geroldi

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 11

Top Venues

Journal of the peripheral nervous system : JPNS

Journal of medical genetics

Orphanet journal of rare diseases

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

Publications

Alessia Mammi, Alessandro Geroldi, Serena Patrone, Fabio Gotta, Paola Origone, Andrea Gaudio, Andrea La Barbera, Francesca Sanguineri, Clarissa Ponti, Michele Iacomino, Monica Traverso, Edoardo Ferlazzo, Angelo Schenone, Angelo Pascarella, Oreste Marsico, Paola Mandich, Emilia Bellone
The neurological core features of the infantile-onset multisystem neurologic, endocrine, and pancreatic disease: A novel nonsense mutation in an Italian family. Journal of the peripheral nervous system : JPNS 29 (2) (2024)
Alessia Mammi, Alessandro Geroldi, Serena Patrone, Fabio Gotta, Paola Origone, Andrea Gaudio, Andrea La Barbera, Francesca Sanguineri, Clarissa Ponti, Michele Iacomino, Monica Traverso, Edoardo Ferlazzo, Angelo Schenone, Angelo Pascarella, Oreste Marsico, Paola Mandich, Emilia Bellone
The neurological core features of the infantile-onset multisystem neurologic, endocrine, and pancreatic disease: A novel nonsense mutation in an Italian family. Journal of the peripheral nervous system : JPNS (2024)
Alessandro Geroldi, Andrea La Barbera, Alessia Mammi, Paola Origone, Andrea Gaudio, Clarissa Ponti, Francesca Sanguineri, Sabrina Matà, Martina Sperti, Ilaria Carboni, Emilia Bellone, Fabio Gotta, Chiara Gemelli, Sara Massucco, Guglielmino Valeria, Lucio Marinelli, Marina Grandis, Giulia Bisogni, Mario Sabatelli, Giuseppe Piscosquito, Gabriella Esposito, Angelo Schenone, Fiore Manganelli, Paola Mandich, Stefano Tozza, Marco Luigetti
Clinical and genetic features of CMT2T in Italian patients confirm the importance of MME pathogenic variants in idiopathic, late-onset axonal neuropathies. Journal of the peripheral nervous system : JPNS (2024)
Alessandro Geroldi, Alessia Mammi, Andrea Gaudio, Serena Patrone, Andrea La Barbera, Paola Origone, Clarissa Ponti, Francesca Sanguineri, Sara Massucco, Lucio Marinelli, Marina Grandis, Angelo Schenone, Paola Mandich, Emilia Bellone, Fabio Gotta
Next-generation sequencing in Charcot-Marie-Tooth: a proposal for improvement of ACMG guidelines for variant evaluation. Journal of medical genetics (2024)
Alessia Mammi, Alessandro Geroldi, Serena Patrone, Fabio Gotta, Paola Origone, Andrea Gaudio, Andrea La Barbera, Francesca Sanguineri, Clarissa Ponti, Michele Iacomino, Monica Traverso, Edoardo Ferlazzo, Angelo Schenone, Angelo Pascarella, Oreste Marsico, Paola Mandich, Emilia Bellone
The neurological core features of the infantile-onset multisystem neurologic, endocrine, and pancreatic disease: A novel nonsense mutation in an Italian family. Journal of the peripheral nervous system : JPNS 29 (2) (2024)
Alessandro Geroldi, Alessia Mammi, Andrea Gaudio, Serena Patrone, Andrea La Barbera, Paola Origone, Clarissa Ponti, Francesca Sanguineri, Sara Massucco, Lucio Marinelli, Marina Grandis, Angelo Schenone, Paola Mandich, Emilia Bellone, Fabio Gotta
Next-generation sequencing in Charcot-Marie-Tooth: a proposal for improvement of ACMG guidelines for variant evaluation. Journal of medical genetics 61 (9) (2024)
Alessandro Geroldi, Alessia Mammi, Andrea Gaudio, Serena Patrone, Andrea La Barbera, Paola Origone, Clarissa Ponti, Francesca Sanguineri, Sara Massucco, Lucio Marinelli, Marina Grandis, Angelo Schenone, Paola Mandich, Emilia Bellone, Fabio Gotta
Next-generation sequencing in Charcot-Marie-Tooth: a proposal for improvement of ACMG guidelines for variant evaluation. Journal of medical genetics 61 (9) (2024)
Alessandro Geroldi, Alessia Mammi, Andrea Gaudio, Serena Patrone, Andrea La Barbera, Paola Origone, Clarissa Ponti, Francesca Sanguineri, Sara Massucco, Lucio Marinelli, Marina Grandis, Angelo Schenone, Paola Mandich, Emilia Bellone, Fabio Gotta
Next-generation sequencing in Charcot-Marie-Tooth: a proposal for improvement of ACMG guidelines for variant evaluation. Journal of medical genetics (2024)
Alessandro Geroldi, Stefano Tozza, Chiara Fiorillo, Maria Nolano, Paola Fossa, Floriana Vitale, Regi Domi, Andrea Gaudio, Alessia Mammi, Serena Patrone, Andrea La Barbera, Paola Origone, Clarissa Ponti, Francesca Sanguineri, Federico Zara, Matteo Cataldi, Vincenzo Salpietro, Consuelo Barbara Venturi, Sara Massucco, Angelo Schenone, Fiore Manganelli, Paola Mandich, Emilia Bellone, Fabio Gotta
A novel de novo variant in POLR3B gene associated with a primary axonal involvement of the largest nerve fibers. Journal of the peripheral nervous system : JPNS (2023)
Alessandro Geroldi, Valeria Prada, Francesca Veneri, Lucia Trevisan, Paola Origone, Marina Grandis, Angelo Schenone, Chiara Gemelli, Paola Lanteri, Paola Fossa, Paola Mandich, Emilia Bellone
Early onset demyelinating Charcot-Marie-Tooth disease caused by a novel in-frame isoleucine deletion in peripheral myelin protein 2. Journal of the peripheral nervous system : JPNS 25 (2) (2020)
Marina Grandis, Alessandro Geroldi, Rossella Gulli, Fiore Manganelli, Fabio Gotta, Merit Lamp, Paola Origone, Lucia Trevisan, Chiara Gemelli, Sabrina Fabbri, Angelo Schenone, Stefano Tozza, Lucio Santoro, Emilia Bellone, Paola Mandich
Autosomal-dominant transthyretin (TTR)-related amyloidosis is not a frequent CMT2 neuropathy "in disguise". Orphanet journal of rare diseases 13 (1) (2018)

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Publication Activity (10 Years)

Top Topics

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Alessandro Geroldi