Dravet syndrome (DS), also known as severe myoclonic epilepsy of infancy (SMEI), is one of
the rare early childhood intractable epileptic encephalopathies associated with pleomorphic …

We conducted a systematic review investigating the efficacy and tolerability of
adrenocorticotropic hormone (ACTH) and corticosteroids in children with epilepsies other …

The benign epilepsy with spinous waves in the central temporal region (BECT) is the one of
the most common epileptic syndromes in children, that seriously threaten the nervous …

It remains unclear to what extent neurodevelopmental disorder (NDD) risk genes retain
functions into adulthood and how they may influence disease phenotypes. SYNGAP1 …

There is increasing recognition that epilepsy can be associated with a broad spectrum of
comorbidities. While epileptic seizures are an essential element of epilepsy in children …

Electrical status epilepticus during slow-wave sleep (ESES) is an epilepsy syndrome with
sleep-induced epileptic discharges and acquired impairment of cognition or behavior. Since …

Electrical status epilepticus during sleep (ESES) is an epileptic encephalopathy in children
with complex clinical manifestations. It is accompanied by specific electroencephalography …

OBJECTIVE: Benign childhood epilepsy with centro-temporal spikes (BCECTS), otherwise
known as benign rolandic epilepsy, is the most common focal epilepsy in childhood. This …

Although interictal spikes (IISs) are a well-established EEG biomarker for epilepsy, whether
they are also a biomarker of cognitive deficits is unclear. Interictal spikes are dynamic events …

Introduction Developmental and/or epileptic encephalopathy with spike-and-wave activation
in sleep (D/EE-SWAS), also referred to as electrical status epilepticus during sleep (ESES) …