Recurrent and non-recurrent mutations of SCN8A in epileptic encephalopathy

Por Jacy L Wagnon, Miriam H Meisler
Publicado em 2015-05-01

Sodium channel SCN8A (Nav1.6): properties and de novo mutations in epileptic encephalopathy and intellectual disability

Por Janelle Elizabeth O'Brien, Miriam H Meisler
Publicado em 2013-10-01

Social Deficits and Cerebellar Degeneration in Purkinje Cell Scn8a Knockout Mice

Por 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
Publicado em 2022-04-01

Genetic interaction between MTMR2 and FIG4 phospholipid phosphatases involved in Charcot-Marie-Tooth neuropathies.

Por 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
Publicado em 2011-10-01

Altered cardiac electrophysiology and SUDEP in a model of Dravet syndrome.

Por 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
Publicado em 2013-01-01