Federico Sicca

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology

Cerebral cortex expansion and folding: what have we learned?

DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants

Malformations of cortical development: clinical features and genetic causes

Translational Research in Epilepsy Genetics

Epilepsy genetics — past, present, and future

NRF2 and NF-қB interplay in cerebrovascular and neurodegenerative disorders: Molecular mechanisms and possible therapeutic approaches

Physiology and Pathophysiology of Sodium Channel Inactivation

Sclerostin: how human mutations have helped reveal a new target for the treatment of osteoporosis

Clinical application of exome sequencing in undiagnosed genetic conditions

Genetic mutations associated with status epilepticus

Affective, neurocognitive and psychosocial disorders associated with traumatic brain injury and post-traumatic epilepsy

Coupling PAF Signaling to Dynein Regulation

Human disorders of cortical development: from past to present

Early-onset familial hemiplegic migraine due to a novel SCN1A mutation

Design and application of an immersive virtual reality system to enhance emotional skills for children with autism spectrum disorders

Application of Internet of Things and Virtual Reality Technology in College Physical Education

Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals

About Sleep's Role in Memory

Pharmacology of the Na _v 1.1 domain IV voltage sensor reveals coupling between inactivation gating processes

Transcriptomes of germinal zones of human and mouse fetal neocortex suggest a role of extracellular matrix in progenitor self-renewal

Phospholipase A₂Enzymes: Physical Structure, Biological Function, Disease Implication, Chemical Inhibition, and Therapeutic Intervention

22q11.2 Microduplication syndrome and epilepsy with continuous spikes and waves during sleep (CSWS). A case report and review of the literature

Internalizing and externalizing symptoms in preschool and school-aged children with epilepsy: Focus on clinical and EEG features

Idiopathic Epilepsies with Seizures Precipitated by Fever and SCN1A Abnormalities

Germline and mosaic mutations of FLN1 in men with periventricular heterotopia

Face processing in children with ASD: Literature review

Mosaic mutations of the LIS1 gene cause subcortical band heterotopia