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Francesca Furia

7PUBLICATIONS
40CO-AUTHORS
NeonatologyGene expression (incl. microarray and other genome-wide approaches)Major global burdens of diseaseSystem and network securityEpigenetics (incl. genome methylation and epigenomics)
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Journal

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

|Aug 18, 2025
Differential outcomes in familial and sporadic SCN8A self-limited infantile epilepsies: Insights from a large international registry.

Francesca Furia, Sopio Gverdtsiteli, Wibke Janzarik

|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

|Oct 03, 2024
Sleep disturbances in SCN8A-related disorders.

Francesca Furia, Katrine M Johannesen, Claudia M Bonardi

|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

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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

Frequent Collaborators

7 joint publications

Elena Gardella

7 joint publications

Rikke S Møller

5 joint publications

Guido Rubboli

3 joint publications

Sopio Gverdtsiteli

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