Area of research
Psychiatry and Mental health · Pediatrics, Perinatology and Child Health
Research interest
Research interests include Epilepsy, Medicine, Psychology, Epilepsy syndromes, Dravet syndrome, and Phenotype.
Updated classification of epileptic seizures: Position paper of the International League Against Epilepsy
Operational definition of developmental and epileptic encephalopathies to underpin the design of therapeutic trials
The epilepsy–autism phenotype associated with developmental and epileptic encephalopathies: New mechanism‐based therapeutic options
Long‐term safety and effectiveness of fenfluramine in children and adults with Dravet syndrome
Trends in epilepsy surgery in Italy before and after the COVID‐19 pandemic: A nationwide study
Outpatient management of prolonged seizures and seizure clusters to prevent progression to a higher‐level emergency: Consensus recommendations of an expert working group
Effects of ganaxolone on non-seizure outcomes in CDKL5 Deficiency Disorder: Double-blind placebo-controlled randomized trial
Practical considerations for the use of fenfluramine to manage patients with Dravet syndrome or Lennox–Gastaut syndrome in clinical practice
Updated clinical recommendations for the management of tuberous sclerosis complex associated epilepsy
Safety and efficacy of cerliponase alfa in children with neuronal ceroid lipofuscinosis type 2 (CLN2 disease): an open-label extension study
Gain of function <i>SCN1A</i> disease‐causing variants: Expanding the phenotypic spectrum and functional studies guiding the choice of effective antiseizure medication
Gain-of-function and loss-of-function variants in <i>GRIA3</i> lead to distinct neurodevelopmental phenotypes
<i>WWOX</i>developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk
A registry for Dravet syndrome: The Italian experience
CDKL5 deficiency disorder: progressive brain atrophy may be part of the syndrome
A real‐life pilot study of the clinical application of pharmacogenomics testing on saliva in epilepsy
Phase-amplitude coupling between low- and high-frequency activities as preoperative biomarker of focal cortical dysplasia subtypes
International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: Position paper by the ILAE Task Force on Nosology and Definitions
ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and Definitions
ILAE definition of the Idiopathic Generalized Epilepsy Syndromes: Position statement by the ILAE Task Force on Nosology and Definitions
Methodology for classification and definition of epilepsy syndromes with list of syndromes: Report of the ILAE Task Force on Nosology and Definitions
International League Against Epilepsy classification and definition of epilepsy syndromes with onset at a variable age: position statement by the ILAE Task Force on Nosology and Definitions
International consensus recommendations for management of new onset refractory status epilepticus (NORSE) including febrile infection‐related epilepsy syndrome (FIRES): Summary and clinical tools
International consensus recommendations for management of new onset refractory status epilepticus including febrile <scp>infection‐related</scp> epilepsy syndrome: Statements and supporting evidence
Individualised prediction of drug resistance and seizure recurrence after medication withdrawal in people with juvenile myoclonic epilepsy: A systematic review and individual participant data meta-analysis
Fenfluramine treatment is associated with improvement in everyday executive function in preschool-aged children (<5 years) with Dravet syndrome: A critical period for early neurodevelopment
Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome
Developmental and epileptic encephalopathies: recognition and approaches to care
Fenfluramine significantly reduces day‐to‐day seizure burden by increasing number of seizure‐free days and time between seizures in patients with Dravet syndrome: A time‐to‐event analysis
Seizure outcome after epilepsy surgery in tuberous sclerosis complex: Results and analysis of predictors from a multicenter study