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Plos Genetics|May 10, 2011
PTG depletion removes Lafora bodies and rescues the fatal epilepsy of Lafora diseaseJulie Turnbull, Anna A DePaoli-Roach, Xiaochu Zhao, et al.Journal of Veterinary Internal Medicine|May 18, 2021
Seizure frequency discrepancy between subjective and objective ictal electroencephalography data in dogsMasayasu Ukai, Thomas Parmentier, Miguel A Cortez, et al.Journal of Child Neurology|July 2, 2011
Treatment of infantile spasms: emerging insights from clinical and basic science perspectivesCarl E Stafstrom, Barry G W Arnason, Tallie Z Baram, et al.Neurobiology of Disease|March 17, 2007
Transgenic mice over-expressing GABA(B)R1a receptors acquire an atypical absence epilepsy-like phenotypeYing Wu, Katherine F Y Chan, James H Eubanks, et al.Epilepsia|August 14, 2019
EEG before and after total corpus callosotomy for pharmacoresistant infantile spasms: Fast oscillations and slow-wave connectivity in hypsarrhythmiaShiro Baba, Vasily A Vakorin, Sam M Doesburg, et al.Proceedings of the National Academy of Sciences of the United States of America|October 26, 2011
Mania-like behavior induced by genetic dysfunction of the neuron-specific Na+,K+-ATPase α3 sodium pumpGreer S Kirshenbaum, Steven J Clapcote, Steven Duffy, et al.Proceedings of the National Academy of Sciences of the United States of America|August 12, 2009
Mutation I810N in the alpha3 isoform of Na+,K+-ATPase causes impairments in the sodium pump and hyperexcitability in the CNSSteven J Clapcote, Steven Duffy, Gang Xie, et al.Proceedings of the National Academy of Sciences of the United States of America|February 23, 2017
Generalized myoclonic epilepsy with photosensitivity in juvenile dogs caused by a defective DIRAS family GTPase 1Franziska Wielaender, Riika Sarviaho, Fiona James, et al.Pageof 6