Serena Lattante
8PUBLICATIONS
14CO-AUTHORS
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Publications (8)
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|Jun 26, 2025
Investigating the Role of B9D1 in Meckel-Gruber Syndrome: A Case Report and Comprehensive Literature Review.Gianluca Campobasso, Ludovica Mercuri, Francesca De Razza
|Jan 08, 2025
Exploring the Role of CCNF Variants in Italian ALS Patients.Giulia Bisogni, Amelia Conte, Umberto Costantino
|Nov 27, 2024
A familial form of Charcot-Marie-Tooth disease (type 2d) caused by a previously unreported variant in GARS1.Dora Varvara, Serena Lattante, Stefania Magri
|Feb 08, 2023
Allele-specific silencing as therapy for familial amyotrophic lateral sclerosis caused by the p.G376D TARDBP mutation.Roberta Romano, Maria De Luca, Victoria Stefania Del Fiore
|Feb 03, 2023
Evaluating the contribution of the gene TARDBP in Italian patients with amyotrophic lateral sclerosis.Serena Lattante, Mario Sabatelli, Giulia Bisogni
|May 28, 2022
Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients.Elisa Perciballi, Federica Bovio, Jessica Rosati
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Frequent Collaborators
2 joint publications
Giuseppe Marangi
2 joint publications
Giulia Bisogni
1 joint publications
Alessia Serrano
1 joint publications
Elisa Perciballi
1 joint publications
Jessica Rosati
1 joint publications
Fabiola De Marchi
1 joint publications
Ivan Lombardi
1 joint publications
Matilde Forcella
1 joint publications
Sabata Martino
1 joint publications
Daniela Ferrari
