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Items: 4

1.
Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series
Maryem Sahli, Abdelali Zrhidri, Siham Chafai Elaloui, Wiam Smaili, Jaber Lyahyai, Fatima Zohra Oudghiri, Abdelaziz Sefiani
J Med Case Rep. 2019; 13: 266. Published online 2019 Aug 23. doi: 10.1186/s13256-019-2203-8
PMCID:
PMC6706917
AbstractArticlePDF–521K
2.
Nav1.1 Localizes to Axons of Parvalbumin-Positive Inhibitory Interneurons: A Circuit Basis for Epileptic Seizures in Mice Carrying an Scn1a Gene Mutation
Ikuo Ogiwara, Hiroyuki Miyamoto, Noriyuki Morita, Nafiseh Atapour, Emi Mazaki, Ikuyo Inoue, Tamaki Takeuchi, Shigeyoshi Itohara, Yuchio Yanagawa, Kunihiko Obata, Teiichi Furuichi, Takao K. Hensch, Kazuhiro Yamakawa
J Neurosci. 2007 May 30; 27(22): 5903–5914. doi: 10.1523/JNEUROSCI.5270-06.2007
PMCID:
PMC6672241
AbstractArticlePDF–1.0M
3.
Diagnostic Yield of Epilepsy Panel Testing in Patients With Seizure Onset Within the First Year of Life
Se Song Jang, Soo Yeon Kim, Hunmin Kim, Hee Hwang, Jong Hee Chae, Ki Joong Kim, Jong-Il Kim, Byung Chan Lim
Front Neurol. 2019; 10: 988. Published online 2019 Sep 13. doi: 10.3389/fneur.2019.00988
PMCID:
PMC6753218
AbstractArticlePDF–761K
4.
Identification of SCN1A and PCDH19 Mutations in Chinese Children with Dravet Syndrome
Anna Ka-Yee Kwong, Cheuk-Wing Fung, Siu-Yuen Chan, Virginia Chun-Nei Wong
PLoS One. 2012; 7(7): e41802. Published online 2012 Jul 25. doi: 10.1371/journal.pone.0041802
PMCID:
PMC3405017
AbstractArticlePDF–504K

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