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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 1, 2020
A P2RX7 single nucleotide polymorphism haplotype promotes exon 7 and 8 skipping and disrupts receptor functionKristen K Skarratt, Ben J Gu, Michael D Lovelace, et al.Proceedings of the National Academy of Sciences of the United States of America|May 31, 2018
Dynamic action potential clamp predicts functional separation in mild familial and severe de novo forms of <i>SCN2A</i> epilepsyGéza Berecki, Katherine B Howell, Yadeesha H Deerasooriya, et al.The Journal of Biological Chemistry|November 10, 2018
Functional consequences of the CAPOS mutation E818K of Na<sup>+</sup>,K<sup>+</sup>-ATPaseChristian P Roenn, Melody Li, Vivien R Schack, et al.Epilepsia|October 29, 2021
Protective effects of medium chain triglyceride diet in a mouse model of Dravet syndromeNikola Jancovski, Tomas Baldwin, Michael Orford, et al.Nature Communications|September 8, 2017
Electron paramagnetic resonance microscopy using spins in diamond under ambient conditionsDavid A Simpson, Robert G Ryan, Liam T Hall, et al.Epilepsia|September 6, 2018
Lack of response to quinidine in KCNT1-related neonatal epilepsyAdam L Numis, Umesh Nair, Anita N Datta, et al.ACS Nano|November 8, 2017
Non-Neurotoxic Nanodiamond Probes for Intraneuronal Temperature MappingDavid A Simpson, Emma Morrisroe, Julia M McCoey, et al.Journal of Virology|July 29, 2011
Amiloride is a competitive inhibitor of coxsackievirus B3 RNA polymeraseElena V Gazina, Eric D Smidansky, Jessica K Holien, et al.Molecular and Cellular Neurosciences|May 1, 2007
A childhood epilepsy mutation reveals a role for developmentally regulated splicing of a sodium channelRuwei Xu, Evan A Thomas, Misty Jenkins, et al.Neurology|December 3, 2017
Precision therapy for epilepsy due to <i>KCNT1</i> mutations: A randomized trial of oral quinidineSaul A Mullen, Patrick W Carney, Annie Roten, et al.Pageof 19