Francesca Furia
Odense, Denmark
Last Updated: 09/26/2026
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Found 15 publications
Neonatal developmental and epileptic encephalopathy with movement disorder and arthrogryposis: A shared phenotype across brain-expressed sodium channelopathies.
Journal: Epilepsia
Published: October 31, 2025
Differential outcomes in familial and sporadic SCN8A self-limited infantile epilepsies: Insights from a large international registry.
Journal: Epilepsia
Published: May 08, 2025
Deciphering the Natural History of SCN8A-Related Disorders.
Journal: Neurology
Published: April 14, 2025
Cyclical Vomiting Syndrome in Individuals With BPTF Haploinsufficiency.
Journal: Pediatric neurology
Published: December 08, 2024
Cenobamate as add-on treatment for SCN8A developmental and epileptic encephalopathy.
Journal: Epilepsia
Published: August 25, 2024
Early mortality in STXBP1-related disorders.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: June 20, 2024
Controlling the Relaxation Dynamics of Polymer Networks by Combining Associative and Dissociative Dynamic Covalent Bonds.
Journal: Advanced materials (Deerfield Beach, Fla.)
Published: May 29, 2024
The phenotypic and genotypic spectrum of individuals with mono- or biallelic ANK3 variants.
Journal: Clinical genetics
Published: May 03, 2024
Quantitative EEG biomarkers for STXBP1-related disorders.
Journal: Epilepsia
Published: March 18, 2024
Emergence of lingual dystonia and strabismus in early-onset SCN8A self-limiting familial infantile epilepsy.
Journal: Epileptic disorders : international epilepsy journal with videotape
Published: December 02, 2023
Epilepsy as a Novel Phenotype of BPTF-Related Disorders.
Journal: Pediatric neurology
Published: September 20, 2023
Last Updated: 09/26/2026