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Epilepsy Research|September 29, 2009
Epilepsy associated with supratentorial brain tumors under 3 years of lifeRoberto Gaggero, Alessandro Consales, Francesca Fazzini, et al.Epilepsia Open|September 12, 2025
Long-term plasma monitoring of THC and CBD in pediatric drug-resistant epilepsy: Implications for cannabidiol therapy with Epidyolex®Alessia Cafaro, Antonella Riva, Federica Pigliasco, et al.Neuroscience and Biobehavioral Reviews|October 21, 2025
Placental omics and neuropsychiatric outcomes: A systematic review of longitudinal human studiesRiccardo Guglielmo, Giulia Sartoris, Pasquale Striano, et al.Epilepsia|June 7, 2014
Co-occurring malformations of cortical development and SCN1A gene mutationsCarmen Barba, Elena Parrini, Roland Coras, et al.Seizure|February 4, 2015
Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variantColoma Tiron, Coloma Tiron de Llano, Oscar Campuzano, et al.Epilepsia|August 1, 2013
Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden deathSara Partemi, Sandrine Cestèle, Marianna Pezzella, et al.Journal of Neurology|February 24, 2019
Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical developmentSara Uccella, Andrea Accogli, Domenico Tortora, et al.Nature Clinical Practice. Neurology|February 8, 2008
Typical progression of myoclonic epilepsy of the Lafora type: a case reportPasquale Striano, Federico Zara, Julie Turnbull, et al.Epilepsy Research|May 27, 2008
Hyperhomocysteinemia and retinal vascular changes in patients with epilepsyVincenzo Belcastro, Pasquale Striano, Daniela Caccamo, et al.Journal of Molecular Medicine (Berlin, Germany)|August 20, 2013
The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonismJose Felix Martí-Massó, Alberto Bergareche, Vladimir Makarov, et al.Pageof 77