Lennox–Gastaut Syndrome (LGS) is a category of severe, disabling epilepsy, characterized
by frequent, treatment-resistant seizures, and cognitive impairment. Electroencephalography …

Summary Objective In patients with Lennox‐Gastaut syndrome (LGS), recurrent epileptic
activity is thought to contribute to impaired cognition (epileptic encephalopathy). Using …

Summary Objective Lennox‐Gastaut syndrome (LGS) is a severe epilepsy phenotype with
characteristic electroclinical features despite diverse etiologies. We previously found …

Purpose: Even if etiologies of Lennox‐Gastaut syndrome (LGS) are diverse, the multiple
causes converge into a final common pathway that results in this specific epilepsy …

Lennox–Gastaut syndrome (LGS) is a severe age-dependent epileptic encephalopathy
usually with onset between 1 and 8 years of age. Functional neuroimaging studies recently …

Objective To identify brain regions underlying interictal generalized paroxysmal fast activity
(GPFA), and their causal interactions, in children and adults with Lennox-Gastaut syndrome …

Objective We aimed to assess the roles of the cortex and thalamus (centromedian nucleus
[CM]) during epileptic activity in Lennox‐Gastaut syndrome (LGS) patients undergoing deep …

Objective To identify abnormal thalamocortical circuits in the severe epilepsy of Lennox–
Gastaut syndrome (LGS) that may explain the shared electroclinical phenotype and provide …

Lennox-Gastaut syndrome (LGS) is a childhood-onset epileptic encephalopathy
characterized by multiple types of medically intractable seizures, cognitive impairment, and …

Lennox-Gastaut syndrome (LGS) is a severe form of childhood-onset epilepsy associated
with high morbidity and mortality. The peak period for manifestations of Lennox-Gastaut …