Reduction of Kcnt1 is therapeutic in mouse models of SCN1A and SCN8A epilepsy by Sophie F. Hill, Sophie F. Hill, Paymaan Jafar-Nejad, Frank Rigo, Miriam H. Meisler, Miriam H. Meisler, Miriam H. Meisler

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Recurrent and non-recurrent mutations of SCN8A in epileptic encephalopathy by Jacy L Wagnon, Miriam H Meisler

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Sodium channel SCN8A (Nav1.6): properties and de novo mutations in epileptic encephalopathy and intellectual disability by Janelle Elizabeth O'Brien, Miriam H Meisler

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Correction of the hypomorphic Gabra2 splice site variant in mouse strain C57BL/6J modifies the severity of Scn8a encephalopathy by Wenxi Yu, Megan K. Mulligan, Robert W. Williams, Miriam H. Meisler

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Reduced Nav1.6 Sodium Channel Activity in Mice Increases In Vivo Sensitivity to Volatile Anesthetics. by Dinesh Pal, Julie M Jones, Stella Wisidagamage, Miriam H Meisler, George A Mashour

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Social Deficits and Cerebellar Degeneration in Purkinje Cell Scn8a Knockout Mice by Xiaofan Yang, Xiaofan Yang, Hongqiang Yin, Hongqiang Yin, Xiaojing Wang, Yueqing Sun, Xianli Bian, Gaorui Zhang, Anning Li, Aihua Cao, Baomin Li, Darius Ebrahimi-Fakhari, Zhuo Yang, Miriam H. Meisler, Miriam H. Meisler, Qiji Liu, Qiji Liu

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A novel de novo mutation of SCN8A (Nav1.6) with enhanced channel activation in a child with epileptic encephalopathy by Mark Estacion, Janelle E. O'Brien, Allison Conravey, Michael F. Hammer, Stephen G. Waxman, Sulayman D. Dib-Hajj, Miriam H. Meisler

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Genetic interaction between MTMR2 and FIG4 phospholipid phosphatases involved in Charcot-Marie-Tooth neuropathies. by Ilaria Vaccari, Giorgia Dina, Hélène Tronchère, Emily Kaufman, Gaëtan Chicanne, Federica Cerri, Lawrence Wrabetz, Bernard Payrastre, Angelo Quattrini, Lois S Weisman, Miriam H Meisler, Alessandra Bolino

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Altered cardiac electrophysiology and SUDEP in a model of Dravet syndrome. by David S Auerbach, Julie Jones, Brittany C Clawson, James Offord, Guy M Lenk, Ikuo Ogiwara, Kazuhiro Yamakawa, Miriam H Meisler, Jack M Parent, Lori L Isom

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Pathogenic mechanism of the FIG4 mutation responsible for Charcot-Marie-Tooth disease CMT4J. by Guy M Lenk, Cole J Ferguson, Clement Y Chow, Natsuko Jin, Julie M Jones, Adrienne E Grant, Sergey N Zolov, Jesse J Winters, Roman J Giger, James J Dowling, Lois S Weisman, Miriam H Meisler

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PI(3,5)P2 biosynthesis regulates oligodendrocyte differentiation by intrinsic and extrinsic mechanisms by Yevgeniya A Mironova, Guy M Lenk, Jing-Ping Lin, Seung Joon Lee, Jeffery L Twiss, Ilaria Vaccari, Alessandra Bolino, Leif A Havton, Sang H Min, Charles S Abrams, Peter Shrager, Miriam H Meisler, Roman J Giger

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Single amino acid deletion in transmembrane segment D4S6 of sodium channel Scn8a (Nav1.6) in a mouse mutant with a chronic movement disorder by Julie M. Jones, Louise Dionne, James Dell'Orco, Rachel Parent, Jamie N. Krueger, Xiaoyang Cheng, Sulayman D. Dib-Hajj, Rosie K. Bunton-Stasyshyn, Lisa M. Sharkey, James J. Dowling, Geoffrey G. Murphy, Vikram G. Shakkottai, Peter Shrager, Miriam H. Meisler

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