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Orphanet Journal of Rare Diseases|March 22, 2023
GLUT1-DS Italian registry: past, present, and future: a useful tool for rare disordersCostanza Varesio, Valentina De Giorgis, Pierangelo Veggiotti, et al.Journal of Neurology|January 10, 2013
PRRT2-related disorders: further PKD and ICCA cases and review of the literatureFelicitas Becker, Julian Schubert, Pasquale Striano, et al.Frontiers in Pediatrics|May 16, 2022
A Phenotypic-Driven Approach for the Diagnosis of WOREE SyndromeAntonella Riva, Giulia Nobile, Thea Giacomini, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 3, 2024
Management, treatment, and clinical approach of Sydenham's chorea in children: Italian survey on expert-based experienceAlessandro Orsini, Andrea Santangelo, Giorgio Costagliola, et al.Journal of Neurology|October 19, 2014
Long-term outcome of epilepsy in patients with Prader-Willi syndromeAlberto Verrotti, Raffaella Cusmai, Daniela Laino, et al.Annals of Neurology|August 19, 2023
Familial Mesial Temporal Lobe Epilepsy: Clinical Spectrum and Genetic Evidence for a Polygenic ArchitectureRebekah V Harris, Karen L Oliver, Piero Perucca, et al.Epilepsia|January 7, 2021
Expanding the phenotype of PIGS-associated early onset epileptic developmental encephalopathyStephanie Efthymiou, Marina Dutra-Clarke, Reza Maroofian, et al.Seizure|January 10, 2013
Lacosamide in pediatric and adult patients: comparison of efficacy and safetyAlberto Verrotti, Giulia Loiacono, Antonella Pizzolorusso, et al.Journal of Neurology|June 14, 2024
CDKL5 deficiency-related neurodevelopmental disorders: a multi-center cohort study in ItalyGiovanni Battista Dell'Isola, Antonella Fattorusso, Francesco Pisani, et al.American Journal of Human Genetics|June 6, 2015
Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsyEmanuela Dazzo, Manuela Fanciulli, Elena Serioli, et al.Pageof 68