Dravet Syndrome

Dravet syndrome, previously known as severe myoclonic epilepsy of infancy (SMEI), is a rare, catastrophic, lifelong form of epilepsy with frequent and/or prolonged seizures that are often triggered by hot temperatures or fever. Discover the latest research on Dravet syndrome here.

February 23, 2021

Revaccination outcomes of children with vaccine proximate seizures.

Lucy DengNicholas Wood
February 17, 2021
Open Access

Clinical Spectrum and Comorbidities of Dravet Syndrome in Taiwan

Chia-Hsuan HuangWang-Tso Lee
February 16, 2021
Open Access

Neuropathological Characterization of a Dravet Syndrome Knock-In Mouse Model Useful for Investigating Cannabinoid Treatments.

Frontiers in Molecular Neuroscience
Valentina SattaOnintza Sagredo
February 14, 2021

The ALOXE3 gene variants from patients with Dravet syndrome decrease gene expression and enzyme activity.

Brain Research Bulletin
Mei-Mei GaoYue-Sheng Long
February 12, 2021
Open Access

The impact of COVID-19 in Dravet syndrome: A UK survey.

Acta Neurologica Scandinavica
Simona BalestriniSanjay M Sisodiya
February 11, 2021

[Analysis of SCN1A gene variants among patients with Dravet syndrome].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Li Li, Dandan Zhu
February 11, 2021
Open Access

Fenfluramine as antiseizure medication for epilepsy.

Developmental Medicine and Child Neurology
Maria Gogou, J Helen Cross
February 10, 2021
Open Access

Cannabidiol in the Treatment of Epilepsy.

Clinical Drug Investigation
Randi von WredeRainer Surges
February 5, 2021
Open Access

Ataluren for drug-resistant epilepsy in nonsense variant-mediated Dravet syndrome and CDKL5 deficiency disorder.

Annals of Clinical and Translational Neurology
Orrin DevinskyDaniel Friedman
February 5, 2021
Open Access

Fenfluramine responder analyses and numbers needed to treat: Translating epilepsy trial data into clinical practice.

European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
Joseph SullivanArnold Gammaitoni
January 31, 2021

Cannabidiol Interactions with Medications, Illicit Substances, and Alcohol: a Comprehensive Review.

Journal of General Internal Medicine
Premalatha BalachandranKevin P Hill
January 22, 2021

The severe epilepsy syndromes of infancy: A population-based study.

Katherine B HowellA Simon Harvey
January 19, 2021

A critical evaluation of fenfluramine hydrochloride for the treatment of Dravet syndrome

Expert Review of Neurotherapeutics
An-Sofie Schoonjans, Berten Ceulemans
January 19, 2021

Efficacy and tolerability of fenfluramine in patients with Dravet syndrome: A systematic review and meta-analysis.

Seizure : the Journal of the British Epilepsy Association
Indar Kumar SharawatKriti Joshi
January 17, 2021

Sleep in Dravet syndrome: A parent-driven survey.

Seizure : the Journal of the British Epilepsy Association
Abigail Van NulandAnne T Berg
January 15, 2021

Foot-floor contact pattern in children and adults with Dravet Syndrome.

Gait & Posture
Lore WyersAlessandra Del Felice

Sign up to follow this feed and discover related papers.

Related Feeds

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.

Acute Disseminated Encephalomyelitis

Acute disseminated encephalomyelitis (ADEM) is a rare inflammatory demyelinating disease of the central nervous system. Discover the latest research on acute disseminated encephalomyelitis here.


Adrenoleukodystrophy (ALD), the most frequent peroxisomal disorder, is an X-linked disorder caused by a defect in the metabolism of long chain fatty acids leading to demyelination, neurodegeneration, and death. Here is the latest research.

Alexander Disease

Alexander disease is a rare leukodystrophy caused by mutations in the astrocyte-specific intermediate filament protein glial fibrillary acidic protein (GFAP). Here is the latest research on this disease.

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.

Asperger Syndrome

Asperger syndrome (AS), also known as Asperger's, is a developmental disorder characterized by significant difficulties in social interaction and nonverbal communication, along with restricted and repetitive patterns of behavior and interests. Discover the latest research on Asperger syndrome here.


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.

Batten Disease

Batten Disease is a group of nervous system disorders known as neuronal ceroid lipofuscinosis. This feed focuses on neurobiological and neuropathological aspects of this disease.

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.

Brain developing: Influences & Outcomes

This feed focuses on influences that affect the developing brain including genetics, fetal development, prenatal care, and gene-environment interactions. Here is the latest research in this field.

© 2021 Meta ULC. All rights reserved