Results 11 to 20 of about 27 (26)

dCas9-Based Scn1a Gene Activation Restores Inhibitory Interneuron Excitability and Attenuates Seizures in Dravet Syndrome Mice

Molecular Therapy, 2020
Gaia Colasante, Gabriele Lignani, Simone Brusco   +2 more
exaly  

Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome

Brain, 2012
Andreas Brunklaus
exaly  

The European patient with Dravet syndrome: Results from a parent-reported survey on antiepileptic drug use in the European population with Dravet syndrome

Epilepsy and Behavior, 2015
Luis MIGUEL Aras
exaly  

The incidence of SCN1A‐related Dravet syndrome in Denmark is 1:22,000: A population‐based study from 2004 to 2009

Epilepsia, 2015
Allan Bayat, Helle Hjalgrim, Rikke S Møller   +2 more
exaly  

Autism in Dravet syndrome: Prevalence, features, and relationship to the clinical characteristics of epilepsy and mental retardation

Epilepsy and Behavior, 2011
Bing-Mei Li, Xiao-Rong Liu, Yong-Hong Yi   +2 more
exaly  

Efficacy of Stiripentol and the Clinical Outcome in Dravet Syndrome

Journal of Child Neurology, 2019
Edibe Pembegul Yıldız, Tuğçe Aksu Uzunhan, Gonca Bektaş   +2 more
exaly  

From genotype to phenotype in Dravet disease

Seizure: the Journal of the British Epilepsy Association, 2017
Svetlana Gataullina, Olivier Dulac
exaly  

Efficacy of antiepileptic drugs for the treatment of Dravet syndrome with different genotypes

Brain and Development, 2016
Xiu-Yu Shi, Yuko Tomonoh, Atsushi Ishii   +2 more
exaly  

A homozygous mutation of voltage‐gated sodium channel β I gene SCN1B in a patient with Dravet syndrome

Epilepsia, 2012
Ikuo Ogiwara, Tetsushi Yamagata, Emi Mazaki   +2 more
exaly  

Convulsive seizures and some behavioral comorbidities are uncoupled in the Scn1aA1783V Dravet syndrome mouse model

Epilepsia, 2020
Saja Fadila, Moshe Giladi, Moran Rubinstein   +2 more
exaly