Similar articles for PMID: 35700297

Year	Number of Results
1998	1
2002	1
2003	1
2004	2
2005	1
2006	1
2007	1
2008	3
2009	5
2010	6
2011	3
2012	6
2013	11
2014	9
2015	5
2016	6
2017	11
2018	4
2019	8
2020	8
2021	5
2022	5
2023	1
2024	3
2025	0

1

Effectiveness of antiseizure therapies in the treatment of Dravet syndrome: Epilepsies in children, young people and adults: Evidence review K.

National Guideline Alliance (UK). National Guideline Alliance (UK). London: National Institute for Health and Care Excellence (NICE); 2022 Apr. London: National Institute for Health and Care Excellence (NICE); 2022 Apr. PMID: 35700297 Free Books & Documents. Review.

2

Myoclonic Absence Seizures in Dravet Syndrome.

Myers KA, Scheffer IE. Myers KA, et al. Pediatr Neurol. 2017 May;70:67-69. doi: 10.1016/j.pediatrneurol.2017.01.004. Epub 2017 Jan 24. Pediatr Neurol. 2017. PMID: 28233668

3

[Clinical features and SCN1A gene mutation analysis of severe myoclonic epilepsy of infancy].

Zhang YH, Sun HH, Liu XY, Ma XW, Yang ZX, Xiong H, Qin J, Lin Q, Wu XR. Zhang YH, et al. Zhonghua Er Ke Za Zhi. 2008 Oct;46(10):769-73. Zhonghua Er Ke Za Zhi. 2008. PMID: 19099883 Chinese.

4

Genetics and clinical correlation of Dravet syndrome and its mimics - experience of a tertiary center in Taiwan.

Liu YH, Cheng YT, Tsai MH, Chou IJ, Hung PC, Hsieh MY, Wang YS, Chen YJ, Kuo CY, Lin JJ, Wang HS, Lin KL. Liu YH, et al. Pediatr Neonatol. 2021 Sep;62(5):550-558. doi: 10.1016/j.pedneo.2021.05.022. Epub 2021 Jun 23. Pediatr Neonatol. 2021. PMID: 34226156 Free article.

5

Sodium Channel Gene Mutations in Children with GEFS+ and Dravet Syndrome: A Cross Sectional Study.

TONEKABONI SH, EBRAHIMI A, BAKHSHANDEH BALI MK, TAHERI OTAGHSARA SM, HOUSHMAND M, NASEHI MM, TAGHDIRI MM, MOGHADDASI M. TONEKABONI SH, et al. Iran J Child Neurol. 2013 Spring;7(2):31-6. Iran J Child Neurol. 2013. PMID: 24665294 Free PMC article.

6

Beyond Dravet Syndrome: Characterization of a Novel, More Severe SCN1A-Linked Epileptic Encephalopathy.

Beck VC, Hull JM, Isom LL. Beck VC, et al. Epilepsy Curr. 2019 Jul-Aug;19(4):266-268. doi: 10.1177/1535759719858339. Epub 2019 Jun 30. Epilepsy Curr. 2019. PMID: 31257984 Free PMC article.

7

[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.

8

A novel SCN1A mutation in a cytoplasmic loop in intractable juvenile myoclonic epilepsy without febrile seizures.

Jingami N, Matsumoto R, Ito H, Ishii A, Ihara Y, Hirose S, Ikeda A, Takahashi R. Jingami N, et al. Epileptic Disord. 2014 Jun;16(2):227-31. doi: 10.1684/epd.2014.0657. Epileptic Disord. 2014. PMID: 24842605 Free article.

9

SCN1A testing for epilepsy: application in clinical practice.

Hirose S, Scheffer IE, Marini C, De Jonghe P, Andermann E, Goldman AM, Kauffman M, Tan NC, Lowenstein DH, Sisodiya SM, Ottman R, Berkovic SF; Genetics Commission of the International League Against Epilepsy. Hirose S, et al. Epilepsia. 2013 May;54(5):946-52. doi: 10.1111/epi.12168. Epub 2013 Apr 15. Epilepsia. 2013. PMID: 23586701 Free article.

10

SCN1A-related phenotypes: Epilepsy and beyond.

Scheffer IE, Nabbout R. Scheffer IE, et al. Epilepsia. 2019 Dec;60 Suppl 3:S17-S24. doi: 10.1111/epi.16386. Epilepsia. 2019. PMID: 31904117 Review.

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