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Frontiers in Neuroscience|June 26, 2020
Loss of Wwox Perturbs Neuronal Migration and Impairs Early Cortical DevelopmentMichele Iacomino, Simona Baldassari, Yuki Tochigi, et al.Genes|December 23, 2023
NUP85 as a Neurodevelopmental Gene: From Podocyte to NeuronAntonella Gambadauro, Giuseppe Donato Mangano, Karol Galletta, et al.Epilepsy & Behavior : E&B|November 5, 2019
Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up studyGiulia Iapadre, Luca Zagaroli, Nicola Cimini, et al.Epilepsy Research|August 9, 2019
Genetic heterogeneity in infantile spasmsAlison M Muir, Candace T Myers, Nancy T Nguyen, et al.International Journal of Legal Medicine|August 15, 2014
Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case seriesSara Partemi, Monica Coll Vidal, Pasquale Striano, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 28, 2021
CASK related disorder: Epilepsy and developmental outcomeThea Giacomini, Sara Nuovo, Ginevra Zanni, et al.Frontiers in Pharmacology|June 28, 2021
Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure MedicationsStefan Wolking, Ciarán Campbell, Caragh Stapleton, et al.Epilepsy & Behavior : E&B|August 2, 2024
Retrospective study on neonatal seizures in a tertiary center of northern Italy after ILAE classification: Incidence, seizure type, EEG and etiologyRobertino Dilena, Maria T Molisso, Agnese De Carli, et al.Epilepsia|January 5, 2026
Memantine treatment in individuals with GRIN gain-of-function variants is associated with improvements in behavior, development, and seizure frequencyMaike Karnstedt, Riley E Perszyk, Scott J Myers, et al.Human Mutation|October 25, 2017
Gain-of-function HCN2 variants in genetic epilepsyMelody Li, Snezana Maljevic, A Marie Phillips, et al.Pageof 68