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Epilepsy & Behavior : E&B|August 12, 2015
CHD2 mutations are a rare cause of generalized epilepsy with myoclonic-atonic seizuresMarina Trivisano, Pasquale Striano, Jacopo Sartorelli, et al.
Stem Cell Research|October 3, 2020
Generation of induced pluripotent stem cell (iPSC) lines from a Joubert syndrome patient with compound heterozygous mutations in C5orf42 geneEltahir Ali, Rosalba Monica Ferraro, Gaetana Lanzi, et al.
Seizure|January 8, 2015
Sporadic and familial glut1ds Italian patients: A wide clinical variabilityValentina De Giorgis, Federica Teutonico, Cristina Cereda, et al.
Seizure|February 16, 2021
The epileptology of Aicardi-Goutières syndrome: electro-clinical-radiological findingsValentina De Giorgis, Costanza Varesio, Maurizio Viri, et al.
Pediatric Neurology|August 6, 2025
Fourteen New Pediatric Cases of Shapiro SyndromeFrancesca Maccarelli, Alice Muda, Elisa Crotti, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 28, 2015
Antiepileptic drugs in Rett SyndromeMaria Pintaudi, Maria Grazia Calevo, Aglaia Vignoli, et al.
Brain & Development|July 6, 2010
Ictal EEG patterns in epilepsy with centro-temporal spikesGiuseppe Capovilla, Francesca Beccaria, Amedeo Bianchi, et al.
Stem Cell Research|June 28, 2021
Establishment of three Joubert syndrome-derived induced pluripotent stem cell (iPSC) lines harbouring compound heterozygous mutations in CC2D2A geneEltahir Ali, Rosalba Monica Ferraro, Adele Guglielmi, et al.
Epilepsia Open|April 12, 2023
Cannabidiol in the acute phase of febrile infection-related epilepsy syndrome (FIRES)Anna Fetta, Elisa Crotti, Elena Campostrini, et al.
Epilepsia Open|February 25, 2026
Fenfluramine in SCN1A-related GEFS+: A multicenter observational study on efficacy, EEG improvement, and tolerabilityGiovanni B Dell'Isola, Alice Muda, Lucio Giordano, et al.
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