Successful treatment of hypothalamic hamartoma (HH) can result in the resolution of its
sequelae including epilepsy and rage attacks. Risks and morbidity of open surgical …

Lennox–Gastaut syndrome (LGS) is a severe form of childhood onset epilepsy in which
patients require multiple medications and may be candidates for palliative surgical …

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

Pediatric epilepsy surgery is underutilized. Only 1%-11% of children with drug resistant
epilepsy (DRE) undergo surgical treatment, or less than half of those estimated to benefit …

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 …

Cognitive dysfunction in children with epilepsy is primarily contributed by etiology, seizures,
frequency of interictal epileptiform discharges, and adverse effects of antiepileptic drugs …

Lennox-Gastaut syndrome is a severe, childhood-onset electroclinical syndrome comprised
of multiple seizure types, intellectual and behavioral disturbances and characteristic findings …

Purpose Hypothalamic hamartomas (HH) are rare benign lesions frequently associated with
gelastic seizures early in life. Epilepsy can progress to multiple seizure types with cognitive …

Abstract Objective: Lennox‐Gastaut syndrome (LGS) is a severe, childhood‐onset epilepsy
that is typically refractory to treatment. We surveyed the current landscape of LGS treatment …

Developmental and epileptic encephalopathies (DEEs) present significant treatment
challenges due to frequent, drug-resistant seizures and comorbidities that impact quality of …