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The Lancet. Neurology|November 15, 2016
MicroRNAs in epilepsy: pathophysiology and clinical utilityDavid C Henshall, Hajo M Hamer, R Jeroen Pasterkamp, et al.
Brain : a Journal of Neurology|February 26, 2016
In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2Susan E Tomlinson, S Veronica Tan, David Burke, et al.
Ebiomedicine|July 20, 2026
Neuron-derived neurotrophic factor-positive interneurons: a cellular target for anti-seizure therapiesAmy Richardson, Marion S Mercier, Yoshiteru Shimoda, et al.
Brain : a Journal of Neurology|January 17, 2022
Gene variant effects across sodium channelopathies predict function and guide precision therapyAndreas Brunklaus, Tony Feng, Tobias Brünger, et al.
Nature Communications|September 4, 2015
Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizuresTommy Stödberg, Amy McTague, Arnaud J Ruiz, et al.
Brain : a Journal of Neurology|June 1, 2010
N-methyl-D-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexesSarosh R Irani, Katarzyna Bera, Patrick Waters, et al.
British Journal of Pharmacology|March 22, 2005
Antagonism of ATP responses at P2X receptor subtypes by the pH indicator dye, Phenol redBrian F King, Min Liu, Andrea Townsend-Nicholson, et al.
Neurology|November 16, 2012
New immunohistochemical method for improved myotonia and chloride channel mutation diagnosticsOlayinka Raheem, Sini Penttilä, Tiina Suominen, et al.
Disease Models & Mechanisms|January 30, 2019
Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalitiesMichelle Stewart, Petrina Lau, Gareth Banks, et al.
Epilepsy & Behavior : E&B|September 18, 2017
Personalized translational epilepsy research - Novel approaches and future perspectives: Part I: Clinical and network analysis approachesFelix Rosenow, Natascha van Alphen, Albert Becker, et al.
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