Childhood absence epilepsy (CAE) is a common pediatric generalized epileptic syndrome.
Although it is traditionally considered as a benign self-limited condition, the apparent benign …

We overview here the new data about the epileptic spectrum disorders within the frame of
perisylvian epileptic network since our first trial to synthetize knowledge about this system …

Objective: The objective of this study is to explore the role of GRIN2A gene in idiopathic
generalized epilepsies and the potential underlying mechanism for phenotypic variation …

Idiopathic or genetic generalized epilepsies (IGE) constitute an electroclinically well‐defined
group that accounts for almost one third of all people with epilepsy. They consist of four well …

Background. Obstructive sleep apnea syndrome (OSAS) affects up to 4% of a pediatric
population, with many comorbidities in the medium‐long term. Functional alterations in the …

Aims CHD4 gene, encoding chromodomain helicase DNA‐binding protein 4, is a vital gene
for fetal development. In this study, we aimed to explore the association between CHD4 …

Aim There is a high demand for information on COVID-19 vaccination for patients with
childhood epilepsy with centrotemporal spikes (BECTS). Patients with this condition need a …

Purpose To investigate whether patients with benign childhood epilepsy with centrotemporal
spikes (BECTS) and childhood absence epilepsy (CAE) show distinct patterns of white …

ABSTRACT Aims. Rolandic (RE), childhood absence (CAE) and juvenile myoclonic (JME)
epilepsy encompass centrotemporal sharp waves, 3‐Hz spike waves and> 3‐Hz spike or …

Objective We describe the evolution of the electroclinical picture of patients with different
types of self-limited epilepsy of childhood (SLEC) occurring at the same or at different times …