Similar articles for PMID: 10742094

Year	Number of Results
1991	1
1998	2
1999	2
2000	4
2001	10
2002	6
2003	4
2004	8
2005	10
2006	7
2007	9
2008	16
2009	19
2010	19
2011	12
2012	3
2013	1
2014	1
2016	1
2019	1
2020	1
2024	0

1

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.

Escayg A, MacDonald BT, Meisler MH, Baulac S, Huberfeld G, An-Gourfinkel I, Brice A, LeGuern E, Moulard B, Chaigne D, Buresi C, Malafosse A. Escayg A, et al. Nat Genet. 2000 Apr;24(4):343-5. doi: 10.1038/74159. Nat Genet. 2000. PMID: 10742094 No abstract available.

2

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.

Wallace RH, Wang DW, Singh R, Scheffer IE, George AL Jr, Phillips HA, Saar K, Reis A, Johnson EW, Sutherland GR, Berkovic SF, Mulley JC. Wallace RH, et al. Nat Genet. 1998 Aug;19(4):366-70. doi: 10.1038/1252. Nat Genet. 1998. PMID: 9697698

3

Generalized epilepsy with febrile seizures plus (GEFS+) spectrum: clinical manifestations and SCN1A mutations in Indonesian patients.

Herini ES, Gunadi, Harahap IS, Yusoff S, Morikawa S, Patria SY, Nishimura N, Sunartini, Sutaryo, Takada S, Matsuo M, Nishio H. Herini ES, et al. Epilepsy Res. 2010 Jun;90(1-2):132-9. doi: 10.1016/j.eplepsyres.2010.04.003. Epub 2010 May 10. Epilepsy Res. 2010. PMID: 20452746

4

Clinical spectrum of SCN1A mutations.

Gambardella A, Marini C. Gambardella A, et al. Epilepsia. 2009 May;50 Suppl 5:20-3. doi: 10.1111/j.1528-1167.2009.02115.x. Epilepsia. 2009. PMID: 19469841 Free article. Review.

5

A case report of a family with overlapping features of autosomal dominant febrile seizures and GEFS+.

Hindocha N, Nabbout R, Elmslie F, Makoff A, Al-Chalabi A, Nashef L. Hindocha N, et al. Epilepsia. 2009 Apr;50(4):937-42. doi: 10.1111/j.1528-1167.2008.01876.x. Epub 2008 Nov 19. Epilepsia. 2009. PMID: 19054398 Free article.

6

Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.

Zucca C, Redaelli F, Epifanio R, Zanotta N, Romeo A, Lodi M, Veggiotti P, Airoldi G, Panzeri C, Romaniello R, De Polo G, Bonanni P, Cardinali S, Baschirotto C, Martorell L, Borgatti R, Bresolin N, Bassi MT. Zucca C, et al. Arch Neurol. 2008 Apr;65(4):489-94. doi: 10.1001/archneur.65.4.489. Arch Neurol. 2008. PMID: 18413471 Free article.

7

A novel inherited mutation in the voltage sensor region of SCN1A is associated with Panayiotopoulos syndrome in siblings and generalized epilepsy with febrile seizures plus.

Livingston JH, Cross JH, Mclellan A, Birch R, Zuberi SM. Livingston JH, et al. J Child Neurol. 2009 Apr;24(4):503-8. doi: 10.1177/0883073808324537. J Child Neurol. 2009. PMID: 19339291

8

A family of generalized epilepsy with febrile seizures plus type 2-a new missense mutation of SCN1A found in the pedigree of several patients with complex febrile seizures.

Nagao Y, Mazaki-Miyazaki E, Okamura N, Takagi M, Igarashi T, Yamakawa K. Nagao Y, et al. Epilepsy Res. 2005 Feb;63(2-3):151-6. doi: 10.1016/j.eplepsyres.2004.11.005. Epilepsy Res. 2005. PMID: 15715999

9

Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?

Scheffer IE, Zhang YH, Jansen FE, Dibbens L. Scheffer IE, et al. Brain Dev. 2009 May;31(5):394-400. doi: 10.1016/j.braindev.2009.01.001. Epub 2009 Feb 8. Brain Dev. 2009. PMID: 19203856 Review.

10

Clinical correlations of mutations in the SCN1A gene: from febrile seizures to severe myoclonic epilepsy in infancy.

Ceulemans BP, Claes LR, Lagae LG. Ceulemans BP, et al. Pediatr Neurol. 2004 Apr;30(4):236-43. doi: 10.1016/j.pediatrneurol.2003.10.012. Pediatr Neurol. 2004. PMID: 15087100

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