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Results: 1 to 20 of 172

1.

A retrospective study of the relation between vaccination and occurrence of seizures in Dravet syndrome.

Tro-Baumann B, von Spiczak S, Lotte J, Bast T, Haberlandt E, Sassen R, Freund A, Leiz S, Stephani U, Boor R, Holthausen H, Helbig I, Kluger G.

Epilepsia. 2011 Jan;52(1):175-8. doi: 10.1111/j.1528-1167.2010.02885.x. Epub 2011 Jan 4.

PMID:
21219303
[PubMed - indexed for MEDLINE]
2.

Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study.

McIntosh AM, McMahon J, Dibbens LM, Iona X, Mulley JC, Scheffer IE, Berkovic SF.

Lancet Neurol. 2010 Jun;9(6):592-8. doi: 10.1016/S1474-4422(10)70107-1. Epub 2010 May 4.

PMID:
20447868
[PubMed - indexed for MEDLINE]
Free Article
3.

Prevalence of SCN1A-related dravet syndrome among children reported with seizures following vaccination: a population-based ten-year cohort study.

Verbeek NE, van der Maas NA, Jansen FE, van Kempen MJ, Lindhout D, Brilstra EH.

PLoS One. 2013 Jun 6;8(6):e65758. doi: 10.1371/journal.pone.0065758. Print 2013.

PMID:
23762420
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Alleged cases of vaccine encephalopathy rediagnosed years later as Dravet syndrome.

Reyes IS, Hsieh DT, Laux LC, Wilfong AA.

Pediatrics. 2011 Sep;128(3):e699-702. doi: 10.1542/peds.2010-0887. Epub 2011 Aug 15.

PMID:
21844054
[PubMed - indexed for MEDLINE]
Free Article
5.

Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome.

Brunklaus A, Ellis R, Reavey E, Forbes GH, Zuberi SM.

Brain. 2012 Aug;135(Pt 8):2329-36. doi: 10.1093/brain/aws151. Epub 2012 Jun 19.

PMID:
22719002
[PubMed - indexed for MEDLINE]
Free Article
6.

Dravet syndrome and vaccination: when science prevails over speculation.

Wiznitzer M.

Lancet Neurol. 2010 Jun;9(6):559-61. doi: 10.1016/S1474-4422(10)70109-5. Epub 2010 May 4. No abstract available.

PMID:
20447869
[PubMed - indexed for MEDLINE]
7.

De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study.

Berkovic SF, Harkin L, McMahon JM, Pelekanos JT, Zuberi SM, Wirrell EC, Gill DS, Iona X, Mulley JC, Scheffer IE.

Lancet Neurol. 2006 Jun;5(6):488-92.

PMID:
16713920
[PubMed - indexed for MEDLINE]
8.

Clinical spectrum of mutations in SCN1A gene: severe myoclonic epilepsy in infancy and related epilepsies.

Fujiwara T.

Epilepsy Res. 2006 Aug;70 Suppl 1:S223-30. Epub 2006 Jun 27. Review.

PMID:
16806826
[PubMed - indexed for MEDLINE]
9.

Dravet syndrome: seizure control and gait in adults with different SCN1A mutations.

Rilstone JJ, Coelho FM, Minassian BA, Andrade DM.

Epilepsia. 2012 Aug;53(8):1421-8. doi: 10.1111/j.1528-1167.2012.03583.x. Epub 2012 Jul 10.

PMID:
22780858
[PubMed - indexed for MEDLINE]
10.

Acute encephalopathy in a patient with Dravet syndrome.

Tsuji M, Mazaki E, Ogiwara I, Wada T, Iai M, Okumura A, Yamashita S, Yamakawa K, Osaka H.

Neuropediatrics. 2011 Feb;42(2):78-81. doi: 10.1055/s-0031-1279725. Epub 2011 Jun 6.

PMID:
21647847
[PubMed - indexed for MEDLINE]
11.

The genetics of Dravet syndrome.

Marini C, Scheffer IE, Nabbout R, Suls A, De Jonghe P, Zara F, Guerrini R.

Epilepsia. 2011 Apr;52 Suppl 2:24-9. doi: 10.1111/j.1528-1167.2011.02997.x. Review.

PMID:
21463275
[PubMed - indexed for MEDLINE]
12.

[Clinical and genetic diagnosis of Dravet syndrome: report of 20 cases].

Siegler Z, Neuwirth M, Hegyi M, Paraicz E, Pálmafy B, Tegzes A, Barsi P, Karcagi V, Claes L, De Jonghe P, Herczegfalvi A, Fogarasi A.

Ideggyogy Sz. 2008 Nov 30;61(11-12):402-8. Hungarian.

PMID:
19070316
[PubMed - indexed for MEDLINE]
13.

Early clinical features in Dravet syndrome patients with and without SCN1A mutations.

Petrelli C, Passamonti C, Cesaroni E, Mei D, Guerrini R, Zamponi N, Provinciali L.

Epilepsy Res. 2012 Mar;99(1-2):21-7. doi: 10.1016/j.eplepsyres.2011.10.010. Epub 2011 Nov 8.

PMID:
22071555
[PubMed - indexed for MEDLINE]
14.

Molecular genetics of Dravet syndrome.

De Jonghe P.

Dev Med Child Neurol. 2011 Apr;53 Suppl 2:7-10. doi: 10.1111/j.1469-8749.2011.03965.x. Review.

PMID:
21504425
[PubMed - indexed for MEDLINE]
15.

Dravet syndrome: from electroclinical characteristics to molecular biology.

Arzimanoglou A.

Epilepsia. 2009 Sep;50 Suppl 8:3-9. doi: 10.1111/j.1528-1167.2009.02228.x.

PMID:
19702726
[PubMed - indexed for MEDLINE]
16.

De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy.

Claes L, Ceulemans B, Audenaert D, Smets K, Löfgren A, Del-Favero J, Ala-Mello S, Basel-Vanagaite L, Plecko B, Raskin S, Thiry P, Wolf NI, Van Broeckhoven C, De Jonghe P.

Hum Mutat. 2003 Jun;21(6):615-21.

PMID:
12754708
[PubMed - indexed for MEDLINE]
17.

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

Ceulemans BP, Claes LR, Lagae LG.

Pediatr Neurol. 2004 Apr;30(4):236-43.

PMID:
15087100
[PubMed - indexed for MEDLINE]
18.

SCN1A mutation screening in adult patients with Lennox-Gastaut syndrome features.

Selmer KK, Lund C, Brandal K, Undlien DE, Brodtkorb E.

Epilepsy Behav. 2009 Nov;16(3):555-7. doi: 10.1016/j.yebeh.2009.08.021. Epub 2009 Sep 24.

PMID:
19782004
[PubMed - indexed for MEDLINE]
19.

Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.

Marini C, Mei D, Temudo T, Ferrari AR, Buti D, Dravet C, Dias AI, Moreira A, Calado E, Seri S, Neville B, Narbona J, Reid E, Michelucci R, Sicca F, Cross HJ, Guerrini R.

Epilepsia. 2007 Sep;48(9):1678-85. Epub 2007 Jun 11.

PMID:
17561957
[PubMed - indexed for MEDLINE]
20.

Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients.

Ragona F, Brazzo D, De Giorgi I, Morbi M, Freri E, Teutonico F, Gennaro E, Zara F, Binelli S, Veggiotti P, Granata T.

Brain Dev. 2010 Jan;32(1):71-7. doi: 10.1016/j.braindev.2009.09.014. Epub 2009 Oct 24.

PMID:
19854600
[PubMed - indexed for MEDLINE]

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