Angéla Kecskés

De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome

Arvid Suls, Johanna A. Jaehn, Angéla Kecskés et al. · The American Journal of Human Genetics · 2013 · 219 citations · Full text

Chd2 Cause, Dravet Syndrome, Molecular Neuroscience +8

Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes

Julian Schubert, Aleksandra Siekierska, Mélanie Langlois et al. · Nature Genetics · 2014 · 195 citations

Neurobiology Of Disease, Neurological Disorder, Genetic Disorder +10

Pharmacological Characterization of an Antisense Knockdown Zebrafish Model of Dravet Syndrome: Inhibition of Epileptic Seizures by the Serotonin Agonist Fenfluramine

Yifan Zhang, Angéla Kecskés, Daniëlle Copmans et al. · PLoS ONE · 2015 · 114 citations · Full text

Serotonin Agonist Fenfluramine, Neurotransmitter, Experimental Pharmacology +16

Serotonergic Modulation as Effective Treatment for Dravet Syndrome in a Zebrafish Mutant Model

Jo Sourbron, H. Schneider, Angéla Kecskés et al. · ACS Chemical Neuroscience · 2016 · 106 citations · Full text

Use of Zebrafish Larvae as a Multi-Endpoint Platform to Characterize the Toxicity Profile of Silica Nanoparticles

Duc-Hung Pham, Bert De Roo, Xuan-Bac Nguyen et al. · Scientific Reports · 2016 · 63 citations · Full text