Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Journal of Alzheimer'S Disease : JAD|May 14, 2026
The bidirectional association of epilepsy with Alzheimer's disease and other neurodegenerative dementias: A longitudinal observational study on the UK BiobankEnrico Fratto, Jolanda Buonocore, Francesco Fortunato, et al.
Neurophysiologie Clinique = Clinical Neurophysiology|March 29, 2024
Quantitative analysis of visually normal EEG reveals spectral power abnormalities in temporal lobe epilepsyMaria Celeste Bonacci, Ilaria Sammarra, Maria Eugenia Caligiuri, et al.
International Journal of Molecular Sciences|May 25, 2024
Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band HeterotopiaRadha Procopio, Francesco Fortunato, Monica Gagliardi, et al.
Stem Cell Research|March 7, 2026
Generation of hiPSCs lines from PRICKLE2-mutant individuals with epilepsyClara Zannino, Antonella Esposito, Mariagrazia Talarico, et al.
Brain Sciences|September 25, 2019
Value of Multimodal Imaging Approach to Diagnosis of NeurosarcoidosisIlaria Sammarra, Gaetano Barbagallo, Angelo Labate, et al.
Epilepsia|May 5, 2025
Focal epilepsy with sensory seizures associated with arginine:glycine amidinotransferase deficiency: A clinical and advanced magnetic resonance imaging studyFrancesco Fortunato, Roberta De Fiores, Ilaria Sammarra, et al.
International Journal of Molecular Sciences|January 11, 2025
Novel KCNQ2 Variants Related to a Variable Phenotypic Spectrum Ranging from Epilepsy with Auditory Features to Severe Developmental and Epileptic EncephalopathiesMariagrazia Talarico, Radha Procopio, Monica Gagliardi, et al.
Genes|November 27, 2024
Two Novel Variants in the CHRNA2 and SCN2A Genes in Italian Patients with Febrile SeizuresRadha Procopio, Monica Gagliardi, Mariagrazia Talarico, et al.
Epilepsia Open|March 13, 2024
May anti-seizure medications alter brain structure in temporal lobe epilepsy? A prospective studyIlaria Sammarra, Maria Eugenia Caligiuri, Maria Celeste Bonacci, et al.
European Journal of Neurology|May 28, 2024
Glucose transporter-1 deficiency syndrome with extreme phenotypic variability in a five-generation family carrying a novel SLC2A1 variantAlessia Giugno, Elena Falcone, Francesco Fortunato, et al.
Pageof 4