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Epilepsia|August 23, 2008
Two novel ALDH7A1 (antiquitin) splicing mutations associated with pyridoxine-dependent seizuresPasquale Striano, Silvia Battaglia, Lucio Giordano, et al.
Seizure|January 8, 2015
Do pure absence seizures occur in myoclonic epilepsy of infancy? A case seriesVincenzo Belcastro, Lucio Giordano, Dario Pruna, et al.
Epilepsy Research|August 23, 2017
Follow-up study of idiopathic generalized epilepsy with associated absence seizure and myoclonic epilepsy of infancyVincenzo Belcastro, Lucio Giordano, Dario Pruna, et al.
Seizure|October 12, 2025
Developmental and epileptic encephalopathy with spike-wave activation in sleep (D/EE-SWAS): Clinical and treatment insights from a cohort of 50 childrenRuzica Kravljanac, Pasquale Striano, Biljana Vucetic Tadic, et al.
Expert Opinion on Emerging Drugs|June 10, 2026
At the forefront of gene-based therapies in dravet syndromeAntonella Riva, Sara Di Gioacchino, Greta Volpedo, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 13, 2010
A pilot open-label trial of zonisamide in Unverricht-Lundborg diseaseDomenico Italiano, Marianna Pezzella, Antonietta Coppola, et al.
Neurology|December 28, 2013
KCNQ2 encephalopathy: delineation of the electroclinical phenotype and treatment responseAdam L Numis, Marco Angriman, Joseph E Sullivan, et al.
Neuropsychiatric Disease and Treatment|June 16, 2017
Ictal blinking, an under-recognized phenomenon: our experience and literature reviewMarco Andrea Nicola Saporito, Giovanna Vitaliti, Piero Pavone, et al.
Epilepsy Research|March 15, 2021
The role of inflammatory mediators in epilepsy: Focus on developmental and epileptic encephalopathies and therapeutic implicationsAlessandro Orsini, Thomas Foiadelli, Giorgio Costagliola, et al.
Frontiers in Neurology|February 3, 2022
The Broad Clinical Spectrum of Epilepsies Associated With Protocadherin 19 Gene MutationGiovanni Battista Dell'Isola, Valerio Vinti, Antonella Fattorusso, et al.
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