Lennox–Gastaut syndrome (LGS) is a severe epileptic and developmental encephalopathy
that is associated with a high rate of morbidity and mortality. It is characterized by multiple …

Encephalopathy with electrical status epilepticus during sleep or ESES is an age-dependent
and self-limited syndrome whose distinctive features include a characteristic age of onset …

Epileptic encephalopathies are severe brain disorders with the epileptic component
contributing to the worsening of cognitive and behavioral manifestations. Acquired epileptic …

The epileptic encephalopathies are conditions in which neurological deterioration is
attributable entirely or partly to epileptic activity and is due to very frequent or severe …

Epileptiform EEG discharges are not confined to people with epilepsy, and their frequency is
only weakly related to severity. A fundamental principle of EEG practice is, therefore, to …

Nine children (five males, four females; age range 6 years 1 month to 11 years 1 month)
affected by benign epilepsy of childhood with centrotemporal or Rolandic spikes (BECRS) …

Objective Epileptic encephalopathy with electrical status epilepticus in sleep (ESES) is a
pediatric epilepsy syndrome with sleep‐induced epileptic discharges and acquired …

Seven children with an unusual epileptic syndrome are reported. The main clinical features
in each patient included onset between 21/2 and six years of age; the occurence of several …

Purpose: The continuous spike and waves during slow‐wave sleep syndrome (CSWSS) and
the Landau‐Kleffner (LKS) syndrome are two rare epileptic encephalopathies sharing …

Purposes: To describe the clinical spectrum and to evaluate the efficacy of different
therapeutic agents in children with electrical status epilepticus in sleep (ESES). Methods …