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Items: 1 to 20 of 92

1.

Mesial temporal sclerosis in children with SCN1A mutation.

Siegler Z, Fogarasi A.

J Child Neurol. 2013 Apr;28(4):541. doi: 10.1177/0883073812473365. No abstract available.

PMID:
23504252
2.

Authors' response to correspondence on "mesial temporal sclerosis in a cohort of children with SCN1A gene mutation".

Van Poppel K, Patay Z, Roberts D, Clarke D, McGregor A, Perkins FF, Wheless J.

J Child Neurol. 2013 Apr;28(4):542. doi: 10.1177/0883073812473509. No abstract available.

PMID:
23504253
3.

Mesial temporal sclerosis in a cohort of children with SCN1A gene mutation.

Van Poppel K, Patay Z, Roberts D, Clarke DF, McGregor A, Perkins FF, Wheless JW.

J Child Neurol. 2012 Jul;27(7):893-7. doi: 10.1177/0883073811435325. Epub 2012 Apr 24.

PMID:
22532537
4.

Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.

Kasperaviciute D, Catarino CB, Matarin M, Leu C, Novy J, Tostevin A, Leal B, Hessel EV, Hallmann K, Hildebrand MS, Dahl HH, Ryten M, Trabzuni D, Ramasamy A, Alhusaini S, Doherty CP, Dorn T, Hansen J, Krämer G, Steinhoff BJ, Zumsteg D, Duncan S, Kälviäinen RK, Eriksson KJ, Kantanen AM, Pandolfo M, Gruber-Sedlmayr U, Schlachter K, Reinthaler EM, Stogmann E, Zimprich F, Théâtre E, Smith C, O'Brien TJ, Meng Tan K, Petrovski S, Robbiano A, Paravidino R, Zara F, Striano P, Sperling MR, Buono RJ, Hakonarson H, Chaves J, Costa PP, Silva BM, da Silva AM, de Graan PN, Koeleman BP, Becker A, Schoch S, von Lehe M, Reif PS, Rosenow F, Becker F, Weber Y, Lerche H, Rössler K, Buchfelder M, Hamer HM, Kobow K, Coras R, Blumcke I, Scheffer IE, Berkovic SF, Weale ME; UK Brain Expression Consortium, Delanty N, Depondt C, Cavalleri GL, Kunz WS, Sisodiya SM.

Brain. 2013 Oct;136(Pt 10):3140-50. doi: 10.1093/brain/awt233. Epub 2013 Sep 6.

5.

Epilepsy: Genetic variant in subtype of MTLE.

Kingwell K.

Nat Rev Neurol. 2013 Nov;9(11):603. doi: 10.1038/nrneurol.2013.206. Epub 2013 Oct 15. No abstract available.

PMID:
24126623
6.

Failure to find association between febrile seizures and SCN1A rs3812718 polymorphism in south Indian patients with mesial temporal lobe epilepsy and hippocampal sclerosis.

Balan S, Vellichirammal NN, Banerjee M, Radhakrishnan K.

Epilepsy Res. 2012 Sep;101(3):288-92. doi: 10.1016/j.eplepsyres.2012.04.009. Epub 2012 May 10.

PMID:
22578703
7.

[Temporal mesial sclerosis syndrome in epilepsy].

Rein AG.

Neurologia. 1998 Mar;13(3):132-44. Review. Spanish.

PMID:
9608221
8.

THE SCN2A gene is not a likely candidate for familial mesial temporal lobe epilepsy.

Maurer-Morelli CV, Secolin R, Marchesini RB, Santos NF, Kobayashi E, Cendes F, Lopes-Cendes I.

Epilepsy Res. 2006 Oct;71(2-3):233-6. Epub 2006 Aug 17.

PMID:
16914293
9.

Neuropsychological lateralization of brain dysfunction in children with mesial temporal sclerosis: a presurgical evaluation.

Kar BR, Rao SL, Chandramouli BA, Thennarasu K, Satishchandra P.

J Child Neurol. 2010 Jun;25(6):705-14. doi: 10.1177/0883073810363998. Epub 2010 Apr 5.

PMID:
20371494
10.

Extrahippocampal temporal lobe atrophy in temporal lobe epilepsy and mesial temporal sclerosis.

Moran NF, Lemieux L, Kitchen ND, Fish DR, Shorvon SD.

Brain. 2001 Jan;124(Pt 1):167-75.

11.

Mesial temporal sclerosis.

Rao MB, Radhakrishnan K.

Neurol India. 1999 Jun;47(2):163. No abstract available.

12.

Prevalence of SCN1A mutations in children with suspected Dravet syndrome and intractable childhood epilepsy.

Wang JW, Shi XY, Kurahashi H, Hwang SK, Ishii A, Higurashi N, Kaneko S, Hirose S; Epilepsy Genetic Study Group Japan.

Epilepsy Res. 2012 Dec;102(3):195-200. doi: 10.1016/j.eplepsyres.2012.06.006. Epub 2012 Jul 20.

PMID:
23195492
13.

Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations.

Carranza Rojo D, Harvey AS, Iona X, Dibbens LM, Damiano JA, Arsov T, Gill D, Freeman JL, Leventer RJ, Vincent A, Berkovic SF, McMahon JM, Scheffer IE.

Epilepsy Res. 2012 Jun;100(1-2):194-8. doi: 10.1016/j.eplepsyres.2012.02.007. Epub 2012 Mar 3.

PMID:
22386634
14.

Idiopathic mesial temporal lobe epilepsy: a syndrome with complex inheritance?

Gomez-Alonso J, Muñoz-Garcia D, Aguado M.

J Neurol. 2009 Dec;256(12):2104-5. doi: 10.1007/s00415-009-5313-1. Epub 2009 Sep 11. No abstract available.

PMID:
19763383
15.

Thalamic changes with mesial temporal sclerosis: MRI.

Deasy NP, Jarosz JM, Elwes RC, Polkey CE, Cox TC.

Neuroradiology. 2000 May;42(5):346-51.

PMID:
10872154
16.

Febrile seizures and mesial temporal sclerosis.

Cendes F.

Curr Opin Neurol. 2004 Apr;17(2):161-4. Review.

PMID:
15021243
17.

A case of autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) coexisting with pervasive developmental disorder harboring SCN1A mutation in addition to CHRNB2 mutation.

Sone D, Sugawara T, Sakakibara E, Tomioka Y, Taniguchi G, Murata Y, Watanabe M, Kaneko S.

Epilepsy Behav. 2012 Oct;25(2):192-5. doi: 10.1016/j.yebeh.2012.07.027. Epub 2012 Sep 29.

PMID:
23032131
18.

De-novo mutations and genetic variation in the SCN1A gene in Malaysian patients with generalized epilepsy with febrile seizures plus (GEFS+).

Tan EH, Razak SA, Abdullah JM, Mohamed Yusoff AA.

Epilepsy Res. 2012 Dec;102(3):210-5. doi: 10.1016/j.eplepsyres.2012.08.004. Epub 2012 Sep 1.

PMID:
22944210
19.

Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome.

Kwong AK, Fung CW, Chan SY, Wong VC.

PLoS One. 2012;7(7):e41802. doi: 10.1371/journal.pone.0041802. Epub 2012 Jul 25.

20.

Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families.

Striano P, Gambardella A, Coppola A, Di Bonaventura C, Bovo G, Diani E, Boaretto F, Egeo G, Ciampa C, Labate A, Testoni S, Passarelli D, Manna I, Sferro C, Aguglia U, Caranci F, Giallonardo AT, Striano S, Nobile C, Michelucci R.

J Neurol. 2008 Jan;255(1):16-23. Epub 2007 Nov 21.

PMID:
18004642
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