Annarita Ferrari

A de novo KCNQ2 Gene Mutation Associated With Non-familial Early Onset Seizures: Case Report and Revision of Literature Data

A. Guzzetta, V. Cetica, S. Fiori, 2019, Front. Pediatr..

No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy

F. Zara, E. Gennaro, M. Elia, 2003, Epilepsy Research.

CASK related disorder: Epilepsy and developmental outcome.

E. Bertini, R. Borgatti, P. Striano, 2021, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Novel translational phenotypes and biomarkers for creatine transporter deficiency

G. Cioni, R. Battini, T. Pizzorusso, 2020, Brain communications.

Self-induced multiple comas with recreational baclofen overdoses in an adolescent girl.

F. Sicca, G. Masi, M. Mucci, 2013, Journal of clinical psychopharmacology.

Epilepsy Course and Developmental Trajectories in STXBP1-DEE

P. Striano, A. Coppola, G. Cantalupo, 2022, Neurology: Genetics.

Psychopathological features in referred adolescents with psychogenic nonepileptic seizures with or without epilepsy

F. Sicca, P. Brovedani, F. Lenzi, 2020, Epilepsy & Behavior.

The Diagnostic Approach to Mitochondrial Disorders in Children in the Era of Next-Generation Sequencing: A 4-Year Cohort Study

C. Bruno, F. Santorelli, R. Battini, 2021, Journal of clinical medicine.

A registry for Dravet syndrome: The Italian experience

E. Lucenteforte, R. Guerrini, T. Granata, 2023, Epilepsia open.

Diagnostic implications of genetic copy number variation in epilepsy plus

H. Mefford, P. Stankiewicz, L. Lagae, 2019, Epilepsia.