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What’s hidden behind Lennox-Gastaut syndrome?

open access: yesЭпилепсия и пароксизмальные состояния, 2020
A number of epileptologists often diagnose Lennox-Gastaut syndrome, while others almost never do. It is necessary to understand why this is happening, especially since Lennox-Gastaut syndrome, according to literature descriptions, is quite common.
E. D. Belousova
doaj   +2 more sources

Diagnostics and age-related evolution of Lennox–Gastaut syndrome. Management in diverse patient age periods

open access: yesЭпилепсия и пароксизмальные состояния, 2022
Lennox–Gastaut syndrome is an epileptic encephalopathy with onset in childhood. The classical triad of diagnostic criteria is well known: 1) presence of various types of refractory epileptic seizures (tonic, atypical absences, myoclonic, tonic/atonic ...
E. D. Belousova   +3 more
doaj   +2 more sources

Fenfluramine for seizures in Dravet syndrome and Lennox-Gastaut syndrome: Mechanisms, clinical evidence, safety, and practical integration [PDF]

open access: yesEpilepsy & Behavior Reports
Developmental and epileptic encephalopathies such as Dravet syndrome and Lennox–Gastaut syndrome remain highly drug resistant and are associated with substantial neurodevelopmental, behavioral, and caregiver burdens.
József Janszky   +2 more
doaj   +2 more sources

Levetiracetam efficacy in patients with Lennox-Gastaut syndrome. Presentation of a case

open access: yesNeurología (English Edition), 2011
Introduction: The Lennox-Gastaut syndrome (LGS) is one of the most severe epileptic encephalopathies of childhood, characterized by electro-clinical triad of generalized peak-slow wave activity (PSW) in the electroencephalogram (EEG), multiple types of ...
A. Díaz Negrillo   +4 more
doaj   +2 more sources

Sleep in Lennox–Gastaut Syndrome: A Scoping Review [PDF]

open access: yesChildren
Background and Objective: Lennox–Gastaut syndrome (LGS) is a severe developmental and epileptic encephalopathy characterized by multiple seizure types, distinctive electroencephalography (EEG) abnormalities, and cognitive impairment.
Debopam Samanta
doaj   +2 more sources

PHARMACOECONOMIC EVALUATION OF RUFINAMIDE USE FOR THE LENNOX-GASTAUT SYNDROME TREATMENT [PDF]

open access: yesФармакоэкономика, 2016
Among epileptic encephalopathies, the Lennox–Gastaut syndrome is considered to be one of the most severe. It is a childhood-onset disease that leads to early disability and mental retardation and is associated with significant costs of medical care and ...
N. K. Mazina   +3 more
doaj   +2 more sources

Current Pharmacologic Strategies for Treatment of Intractable Epilepsy in Children [PDF]

open access: yesInternational Neurourology Journal, 2021
Epileptic encephalopathy (EE) is a devastating pediatric disease that features medically resistant seizures, which can contribute to global developmental delays.
Ja Un Moon, Kyung-Ok Cho
doaj   +1 more source

The surgical treatment improving at Lennox–Gastaut syndrome

open access: yesUkrainian Neurosurgical Journal, 2007
The modern sights of Lennox–Gastaut syndrome management are given. The surgical methods, used in Lennox–Gastaut syndrome treatment are described.
A. O. Laponogov   +2 more
doaj   +1 more source

Lennox-Gastaut and Schizophrenia: Comorbidity or complication?

open access: yesEuropean Psychiatry, 2022
Introduction Lennox-Gastaut syndrome (LGS) belongs to the group of severe childhood epileptic encephalopathies and represents 1 to 2% of all childhood epilepsies.It is characterized by the occurrence of generalized epileptic seizures, characterized by a
Z. Bencharfa   +4 more
doaj   +1 more source

Eficacia del levetiracetam en pacientes con síndrome de Lennox-Gastaut. Presentación de un caso

open access: yesNeurología, 2011
Resumen: Introducción: El síndrome de Lennox-Gastaut (SLG) es una de las encefalopatías epilépticas más severas de la infancia, caracterizada por la tríada electroclínica de actividad generalizada de punta onda lenta (POL) en el electroencefalograma ...
A. Díaz Negrillo   +4 more
doaj   +1 more source

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