Francesca Sardina

5PUBLICATIONS
10CO-AUTHORS
Neurology and neuromuscular diseasesGene and molecular therapy
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Publications (5)

|Sep 03, 2026
Validation of a Cellular Imaging-Based Method as a Potential Biomarker for SPG4 Hereditary Spastic Paraplegia.

|Mar 02, 2026
Mutation type-specific transcriptomic signatures and readthrough therapy rescue in SMC1A-related developmental and epileptic encephalopathy.

Maddalena Di Nardo, Francesca Sardina, Maria M Pallotta

|Feb 07, 2025
Targeting MDM2 affects spastin protein levels and functions: implications for HSP treatment.

Francesca Sardina, Federica Polverino, Sonia Valentini

|Feb 23, 2023
New cellular imaging-based method to distinguish the SPG4 subtype of hereditary spastic paraplegia.

Francesca Sardina, Davide Valente, Gaia Fattorini

|Oct 27, 2020
Spastin recovery in hereditary spastic paraplegia by preventing neddylation-dependent degradation.

Francesca Sardina, Alessandra Pisciottani, Manuela Ferrara

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Frequent Collaborators

4 joint publications

Cinzia Rinaldo

1 joint publications

Davide Valente

1 joint publications

Fabiola Moretti

1 joint publications

Alessandro Paiardini