Lennox-Gastaut Syndrome

Lennox-Gastaut syndrome is a rare epileptic syndrome characterized by multiple types of seizures, developmental delay, and cognitive impairment. It can be caused by trauma, infections, metabolic disorders, or genetic factors. Find the latest research on Lennox-Gastaut syndrome here.

January 17, 2020

Source of cannabinoids: what is available, what is used, and where does it come from?

Epileptic Disorders : International Epilepsy Journal with Videotape
Nicola SpecchioHelen J Cross
May 14, 2020

Stereotactic laser anterior corpus callosotomy for Lennox-Gastaut syndrome

Epilepsia
James X TaoPeter C Warnke
December 20, 2019
Open Access

Homozygous STXBP1 variant causes encephalopathy and gain-of-function in synaptic transmission

Brain : a Journal of Neurology
Hanna C A LammertseFederico Zara
May 1, 2020

RNAi-Based Gene Therapy Rescues Developmental and Epileptic Encephalopathy in a Genetic Mouse Model

Molecular Therapy : the Journal of the American Society of Gene Therapy
Osasumwen V AimiuwuWayne N Frankel
January 17, 2020

Adverse effects of cannabinoids

Epileptic Disorders : International Epilepsy Journal with Videotape
Carla Anciones, Antonio Gil-Nagel
January 3, 2020
Review

Cannabis for Pediatric Epilepsy

Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society
Richard J HuntsmanAlan E Shackelford
May 30, 2020
Open Access

GABAA receptor β3 subunit mutation D120N causes Lennox-Gastaut syndrome in knock-in mice

Brain Communications
Shimian QuRobert L Macdonald
February 13, 2020

What has been the impact of new drug treatments on epilepsy?

Current Opinion in Neurology
Zhibin ChenPatrick Kwan
November 12, 2019

New anti-epileptic drugs in Paediatrics

Anales de pediatría : publicación oficial de la Asociación Española de Pediatría (A.E.P.)
Ignacio MálagaJuan José García-Peñas
January 11, 2020

The proposed mechanism of action of CBD in epilepsy

Epileptic Disorders : International Epilepsy Journal with Videotape
Roy A Gray, Ben J Whalley
February 6, 2020

Clinical features and electroclinical evolution in 22 cases with epileptic spasms without hypsarrhythmia

Epileptic Disorders : International Epilepsy Journal with Videotape
Reiko KoichiharaRyuki Matsuura
November 4, 2019
Case Report

CHD2-related epilepsy: novel mutations and new phenotypes

Developmental Medicine and Child Neurology
Jiaoyang ChenYuehua Zhang
February 14, 2020

The proposed mechanisms of action of CBD in epilepsy

Epileptic Disorders : International Epilepsy Journal with Videotape
Royston A Gray, Benjamin J Whalley
October 18, 2019
PreprintOpen Access

Targeting the centromedian thalamic nucleus for deep brain stimulation

medRxiv
Aaron E L WarrenJohn Archer
February 28, 2020
ReviewOpen Access

Cannabinoids in the Treatment of Epilepsy: Current Status and Future Prospects

Neuropsychiatric Disease and Treatment
Alessandra MoranoCarlo Di Bonaventura
February 22, 2020
Open Access

Effective and safe diet therapies for Lennox-Gastaut syndrome with mitochondrial dysfunction

Therapeutic Advances in Neurological Disorders
Ji-Hoon NaYoung-Mock Lee
February 26, 2020

Epilepsy and cannabidiol: a guide to treatment

Epileptic Disorders : International Epilepsy Journal with Videotape
Alexis ArzimanoglouCollaborators

Sign up to follow this feed and discover related papers.

Related Feeds

22q11 Deletion Syndrome

22q11.2 deletion syndrome, also known as DiGeorge syndrome, is a congenital disorder caused as a result of a partial deletion of chromosome 22. Here is the latest research.

4H Leukodystrophy

4H Lekodystrophy involves hypomyelination, hypogonadotropic hypogonadism and hypodontia. It is also known as POLR-3Related Leukodystrophy. 4H syndrome symptoms include delayed or abnormal puberty, issues with central nervous system signal transmission, abnormal development of teeth, and symptoms tend to progressively get worse over time. There is not yet a known cure.

ALS

Amyotrophic Lateral Sclerosis (ALS), also known as motor neuron disease, is associated with the death of neurons that control voluntary muscles. Discover the latest research on ALS here.

Absence Epilepsy

Absence epilepsy is a common seizure disorder in children which can produce chronic psychosocial sequelae. Discover the latest research on absence epilepsies here.

Adenomatous Polyposis Coli

Adenomatous polyposis coli is a protein encoded by the APC gene and acts as a tumor suppressor. Discover the latest research on adenomatous polyposis coli here.

Adult Polyglucosan Body Disease

Adult polyglucosan body disease (APBD) is a rare autosomal recessive disease characterized by defects in the glycogen brancher enzyme 1 (GBE1) gene. Discover the latest research on APBD here.

Alzheimer's Disease: Abeta

Alzheimer's disease (AD) is a chronic neurodegenerative disease associated with accumulation of amyloid plaques, which are comprised of amyloid beta. Here is the latest research in this field.

Angelman Syndrome

Angelman syndrome is a neurogenetic imprinting disorder caused by loss of the maternally inherited UBE3A gene and is characterized by generalized epilepsy, limited expressive speech, sleep dysfunction, and movement disorders. Here is the latest research.

Autism

Autism spectrum disorder is associated with challenges with social skills, repetitive behaviors, and often accompanied by sensory sensitivities and medical issues. Here is the latest research.

Benign Rolandic Epilepsy

Benign Rolandic epilepsy is a partial idiopathic epilepsy of childhood presenting with a nocturnal seizure and with a typical EEG showing centrotemporal spike and multifocal or generalized sharp slow waves. Here is the latest research.

© 2020 Meta ULC. All rights reserved
/feed-previews/lennox-gastaut-syndrome/e974647a-67d4-4d1a-8d2f-dafaa35c456f