Showing results (41-50 of 183) with videos related to
Sort By:
Pageof 19
The Journal of Physiology|April 9, 2010
Neurological channelopathies: new insights into disease mechanisms and ion channel functionDimitri M Kullmann, Stephen G WaxmanInternational Review of Neurobiology|August 1, 2014
From treatment to cure: stopping seizures, preventing seizures, and reducing brain propensity to seizeIvan Pavlov, Stephanie SchorgeNeuroscience|March 19, 2022
Gene Therapy for Neurological Disease: State of the Art and Opportunities for Next-generation ApproachesGareth Morris, Stephanie SchorgeThe Journal of Neuroscience : the Official Journal of the Society for Neuroscience|February 25, 2003
Studies of NMDA receptor function and stoichiometry with truncated and tandem subunitsStephanie Schorge, David ColquhounThe Journal of Physiology|February 17, 2010
Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsySanjeev Rajakulendran, Tracey D Graves, Robyn W Labrum, et al.Cells|July 6, 2023
Basket to Purkinje Cell Inhibitory Ephaptic Coupling Is Abolished in Episodic Ataxia Type 1Henry G S Martin, Dimitri M KullmannEbiomedicine|May 13, 2019
Designer receptor technology for the treatment of epilepsyAndreas Lieb, Mikail Weston, Dimitri M KullmannScientific Reports|November 28, 2019
Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutationMichael G Thor, Vinojini Vivekanandam, Marisol Sampedro-Castañeda, et al.FEBS Letters|May 17, 2015
Changing channels in pain and epilepsy: Exploiting ion channel gene therapy for disorders of neuronal hyperexcitabilityAlbert Snowball, Stephanie SchorgeBrain : a Journal of Neurology|September 16, 2021
Translating genetic and functional data into clinical practice: a series of 223 families with myotoniaKaren Suetterlin, Emma Matthews, Richa Sud, et al.Pageof 19