Similar articles for PMID: 19763161

Year	Number of Results
2000	1
2001	7
2002	3
2003	4
2004	4
2005	4
2006	8
2007	7
2008	7
2009	12
2010	32
2011	24
2012	19
2013	18
2014	12
2015	5
2016	7
2017	4
2018	7
2019	10
2020	9
2021	21
2022	27
2023	8
2024	0

1

A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome.

Singh NA, Pappas C, Dahle EJ, Claes LR, Pruess TH, De Jonghe P, Thompson J, Dixon M, Gurnett C, Peiffer A, White HS, Filloux F, Leppert MF. Singh NA, et al. PLoS Genet. 2009 Sep;5(9):e1000649. doi: 10.1371/journal.pgen.1000649. Epub 2009 Sep 18. PLoS Genet. 2009. PMID: 19763161 Free PMC article.

2

Mutations in the sodium channel genes SCN1A, SCN3A, and SCN9A in children with epilepsy with febrile seizures plus(EFS+).

Ma H, Guo Y, Chen Z, Wang L, Tang Z, Zhang J, Miao Q, Zhai Q. Ma H, et al. Seizure. 2021 May;88:146-152. doi: 10.1016/j.seizure.2021.04.006. Epub 2021 Apr 9. Seizure. 2021. PMID: 33895391 Free article.

3

Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome.

Mulley JC, Hodgson B, McMahon JM, Iona X, Bellows S, Mullen SA, Farrell K, Mackay M, Sadleir L, Bleasel A, Gill D, Webster R, Wirrell EC, Harbord M, Sisodiya S, Andermann E, Kivity S, Berkovic SF, Scheffer IE, Dibbens LM. Mulley JC, et al. Epilepsia. 2013 Sep;54(9):e122-6. doi: 10.1111/epi.12323. Epub 2013 Jul 29. Epilepsia. 2013. PMID: 23895530 Free article.

4

[Phenotype and SCN1A gene mutation screening in 39 families with generalized epilepsy with febrile seizures plus].

Xu XJ, Zhang YH, Sun HH, Liu XY, Wu HS, Wu XR. Xu XJ, et al. Zhonghua Er Ke Za Zhi. 2012 Aug;50(8):580-6. Zhonghua Er Ke Za Zhi. 2012. PMID: 23158734 Chinese.

5

Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel alpha 1 subunit gene, SCN1A.

Ito M, Nagafuji H, Okazawa H, Yamakawa K, Sugawara T, Mazaki-Miyazaki E, Hirose S, Fukuma G, Mitsudome A, Wada K, Kaneko S. Ito M, et al. Epilepsy Res. 2002 Jan;48(1-2):15-23. doi: 10.1016/s0920-1211(01)00313-8. Epilepsy Res. 2002. PMID: 11823106

6

Neuronal voltage-gated ion channels are genetic modifiers of generalized epilepsy with febrile seizures plus.

Hawkins NA, Martin MS, Frankel WN, Kearney JA, Escayg A. Hawkins NA, et al. Neurobiol Dis. 2011 Mar;41(3):655-60. doi: 10.1016/j.nbd.2010.11.016. Epub 2010 Dec 13. Neurobiol Dis. 2011. PMID: 21156207 Free PMC article.

7

SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus.

Sun H, Zhang Y, Liang J, Liu X, Ma X, Wu H, Xu K, Qin J, Qi Y, Wu X. Sun H, et al. J Hum Genet. 2008;53(8):769-774. doi: 10.1007/s10038-008-0306-y. Epub 2008 Jun 20. J Hum Genet. 2008. PMID: 18566737

8

Epilepsy phenotype associated with a chromosome 2q24.3 deletion involving SCN1A: Migrating partial seizures of infancy or atypical Dravet syndrome?

Lim BC, Hwang H, Kim H, Chae JH, Choi J, Kim KJ, Hwang YS, Yum MS, Ko TS. Lim BC, et al. Epilepsy Res. 2015 Jan;109:34-9. doi: 10.1016/j.eplepsyres.2014.10.008. Epub 2014 Oct 28. Epilepsy Res. 2015. PMID: 25524840

9

A novel SCN1A mutation associated with generalized epilepsy with febrile seizures plus--and prevalence of variants in patients with epilepsy.

Escayg A, Heils A, MacDonald BT, Haug K, Sander T, Meisler MH. Escayg A, et al. Am J Hum Genet. 2001 Apr;68(4):866-73. doi: 10.1086/319524. Epub 2001 Mar 14. Am J Hum Genet. 2001. PMID: 11254445 Free PMC article.

10

SCN9A Epileptic Encephalopathy Mutations Display a Gain-of-function Phenotype and Distinct Sensitivity to Oxcarbazepine.

Zhang S, Zhang Z, Shen Y, Zhu Y, Du K, Guo J, Ji Y, Tao J. Zhang S, et al. Neurosci Bull. 2020 Jan;36(1):11-24. doi: 10.1007/s12264-019-00413-5. Epub 2019 Aug 1. Neurosci Bull. 2020. PMID: 31372899 Free PMC article.

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