Results 31 to 40 of about 1,156,270 (203)

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

Neurología, 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, F. Martín del Valle, M. González Salaices, C. Prieto Jurczynska, J. Carneado Ruiz   +4 more
doaj   +1 more source

Therapies for Lennox-Gastaut syndrome [PDF]

Srpski Arhiv za Celokupno Lekarstvo, 2005
The treatment of Lennox-Gastaut Syndrome (LGS) has been improved with the introduction of the new anti-epileptic drugs: lamotrigine and topiramate, the employment of a ketogenic diet, and the availability of vagal nerve stimulation.
Đurić Milena
doaj   +1 more source

Improved seizure control and regaining cognitive milestones after vagus nerve stimulation revision surgery in Lennox–Gastaut syndrome

Epilepsy and Behavior Case Reports, 2018
We report a child with Lennox–Gastaut syndrome with an increase in seizure frequency and loss of psychomotor skills due to a disintegrated cervical VNS lead, not detected during standard device monitoring.
Hilde M. Braakman, Joke Creemers, Danny M. Hilkman, Sylvia Klinkenberg, Suzanne M. Koudijs, Mariette Debeij-van Hall, Erwin M. Cornips   +6 more
doaj   +1 more source

Efficacy and Safety of Lamotrigine Adjunctive Therapy in Lennox-Gastaut Syndrome [PDF]

Annals of Child Neurology, 2023
Purpose Lamotrigine (LTG) is often used as adjunctive therapy in Lennox-Gastaut syndrome (LGS); however, it may worsen myoclonic and atypical absence seizures in LGS patients.
Hui Jin Shin, Ara Ko, Se Hee Kim, Joon Soo Lee, Heung Dong Kim, Hoon-Chul Kang   +5 more
doaj   +1 more source

Lennox-Gastaut Syndrome Associated with Unilateral Hemispheric Porencephaly [PDF]

, 2010
We report an 18 year-old male with a hemispheric large porencephaly who demonstrated symptomaticWest syndrome and then developed into Lennox-Gastaut syndrome.
Imataka, George, Ogino, Masahiro, Kuwashima, Shigeo, Hashimoto, Teisuke, Watabe, Yoshiyuki, Arisaka, Osamu   +5 more
core   +1 more source

Clinical burden and treatment patterns associated with Dravet or Lennox-Gastaut syndromes: A retrospective study using natural language processing of narrative unstructured electronic health records

Heliyon
Introduction: This study aimed to investigate the clinical and humanistic burden in two developmental and epileptic encephalopathies, Dravet syndrome and Lennox-Gastaut syndrome, and describe challenges related to treatment with antiseizure medications ...
Mei Lu, Dave Iwanyckyj, Sally W. Wade, Pablo Racana, Fernando Otalora, Satish Rao   +5 more
doaj   +1 more source

Lennox-Gastaut Syndrome: In a Nutshell

, 2018
Lennox-Gastaut syndrome is one of the rare childhood-onset epileptic encephalopathies, characterized by multiple type seizure disorder, the typical pattern on electroencephalogram and intellectual disability. Tonic-type seizures are most commonly seen in
Jahngir, Muhammad Umair, Jahangir, Memoona, Ahmad, Malik Qistas   +2 more
core   +1 more source

Rufinamide Use in Refractory Epilepsies

Archives of Epilepsy, 2015
The drug rufinamide was approved in November 2008 by the US Food and Drug Administration for use in the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome in patients older than 4 years.
Abidin ERDAL, Yasemin AYDEMİR, F. Ezgi UÇAN TOKUÇ, Gizem ÖZDEMİR, Gülnihal KUTLU, Fatma GENÇ, Yasemin BİÇER GÖMCELİ   +6 more
doaj   +1 more source

Multifocal Independent Spike Syndrome

Pediatric Neurology Briefs, 1995
The relationship of the syndrome of multifocal independent spikes (MIS) to hypsarrhythmia and the slow spike-wave (Lennox-Gastaut) syndrome was studied in 64 children with MIS examined during a 3-year period at the Cleveland Clinic, Ohio.
J Gordon Millichap
doaj   +1 more source

Sleep and respiratory abnormalities in adults with developmental and epileptic encephalopathies using polysomnography and video‐EEG monitoring

Epilepsia Open, 2023
This study evaluated sleep and respiratory abnormalities, and their relationship with seizures, in adults with developmental and epileptic encephalopathies (DEEs).
Shobi Sivathamboo, Kenneth A. Myers, Andreas Pattichis, Elise J. White, Ka Nyuk Ku, Terence J. O'Brien, Piero Perucca, Patrick Kwan   +7 more
doaj   +1 more source