Francesca Furia
7PUBLICATIONS
40CO-AUTHORS
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Publications (7)
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|Apr 02, 2026
Neonatal developmental and epileptic encephalopathy with movement disorder and arthrogryposis: A shared phenotype across brain-expressed sodium channelopathies.Sopio Gverdtsiteli, Sebastian Ortiz, Tobias Brünger
|Jan 15, 2025
Cenobamate as add-on treatment for SCN8A developmental and epileptic encephalopathy.Cathrine E Gjerulfsen, Madeleine J Oudin, Francesca Furia
|Oct 28, 2024
Quantitative EEG biomarkers for STXBP1-related disorders.Alberto Cossu, Francesca Furia, Jacopo Proietti
|Mar 04, 2024
Emergence of lingual dystonia and strabismus in early-onset SCN8A self-limiting familial infantile epilepsy.Caterina Ancora, Juan Dario Ortigoza-Escobar, Margherita Aluffi Valletti
|Apr 28, 2023
IRF2BPL as a novel causative gene for progressive myoclonus epilepsy.Elena Gardella, Roberto Michelucci, Hanne M Christensen
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Frequent Collaborators
7 joint publications
Elena Gardella
7 joint publications
Rikke S Møller
5 joint publications
Guido Rubboli
3 joint publications
Sopio Gverdtsiteli
3 joint publications
Roberto Previtali
2 joint publications
Caterina Ancora
2 joint publications
Jacopo Proietti
2 joint publications
Angel Aledo-Serrano
1 joint publications
Roberto Michelucci
1 joint publications
Chiara Reale
