Literature DB >> 30903923

Migrating focal seizures in Autosomal Dominant Sleep-related Hypermotor Epilepsy with KCNT1 mutation.

Matteo Cataldi1, Lino Nobili2, Federico Zara3, Romina Combi4, Giulia Prato5, Thea Giacomini6, Valeria Capra7, Patrizia De Marco8, Luigi Ferini-Strambi9, Maria Margherita Mancardi10.   

Abstract

Entities:  

Keywords:  Focal seizure; KCNT1 gene; Migrating seizure; Sleep-related hypermotor epilepsy

Mesh：

Substances：

Year:  2019        PMID： 30903923     DOI： 10.1016/j.seizure.2019.02.019

Source DB:  PubMed          Journal:  Seizure        ISSN： 1059-1311            Impact factor:   3.184


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  4 in total

Review 1.  [Advances in sleep-related hypermotor epilepsy].

Authors:  Jiahui Xu; Bo Jin; Lisan Zhang; Shuang Wang
Journal:  Zhejiang Da Xue Xue Bao Yi Xue Ban       Date:  2020-08-25

2.  The phenotypic spectrum of KCNT1: a new family with variable epilepsy syndromes including mild focal epilepsy.

Authors:  Christina Cherian; Juan P Appendino; Setareh Ashtiani; Paolo Federico; Christine P Molnar; Marina Kerr; Aneal Khan; Ping Yee Billie Au; Karl Martin Klein
Journal:  J Neurol       Date:  2021-09-19       Impact factor: 4.849

3.  Structure-Based Identification and Characterization of Inhibitors of the Epilepsy-Associated KNa1.1 (KCNT1) Potassium Channel.

Authors:  Bethan A Cole; Rachel M Johnson; Hattapark Dejakaisaya; Nadia Pilati; Colin W G Fishwick; Stephen P Muench; Jonathan D Lippiat
Journal:  iScience       Date:  2020-04-25

4.  Slo2 potassium channel function depends on RNA editing-regulated expression of a SCYL1 protein.

Authors:  Long-Gang Niu; Ping Liu; Zhao-Wen Wang; Bojun Chen
Journal:  Elife       Date:  2020-04-21       Impact factor: 8.140
  4 in total

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