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Results: 1 to 20 of 36

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.

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]
3.

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]
4.

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]
5.

Adults with a history of possible Dravet syndrome: an illustration of the importance of analysis of the SCN1A gene.

Verbeek NE, van Kempen M, Gunning WB, Renier WO, Westland B, Lindhout D, Brilstra EH.

Epilepsia. 2011 Apr;52(4):e23-5. doi: 10.1111/j.1528-1167.2011.02982.x. Epub 2011 Mar 3. Review.

PMID:
21371021
[PubMed - indexed for MEDLINE]
6.

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

Scheffer IE, Zhang YH, Jansen FE, Dibbens L.

Brain Dev. 2009 May;31(5):394-400. doi: 10.1016/j.braindev.2009.01.001. Epub 2009 Feb 8. Review.

PMID:
19203856
[PubMed - indexed for MEDLINE]
7.

Borderline Dravet syndrome: a useful diagnostic category?

Guerrini R, Oguni H.

Epilepsia. 2011 Apr;52 Suppl 2:10-2. doi: 10.1111/j.1528-1167.2011.02995.x. Review.

PMID:
21463273
[PubMed - indexed for MEDLINE]
8.

Dravet syndrome and SCN1A gene mutation related-epilepsies: cognitive impairment and its determinants.

Guerrini R, Falchi M.

Dev Med Child Neurol. 2011 Apr;53 Suppl 2:11-5. doi: 10.1111/j.1469-8749.2011.03966.x. Review.

PMID:
21504426
[PubMed - indexed for MEDLINE]
9.

The core Dravet syndrome phenotype.

Dravet C.

Epilepsia. 2011 Apr;52 Suppl 2:3-9. doi: 10.1111/j.1528-1167.2011.02994.x. Review.

PMID:
21463272
[PubMed - indexed for MEDLINE]
10.

Progressive neurocognitive decline in two children with Dravet syndrome, de novo SCN1A truncations and different epileptic phenotypes.

Riva D, Vago C, Pantaleoni C, Bulgheroni S, Mantegazza M, Franceschetti S.

Am J Med Genet A. 2009 Oct;149A(10):2339-45. doi: 10.1002/ajmg.a.33029. Review.

PMID:
19764027
[PubMed - indexed for MEDLINE]
11.

Epileptic encephalopathies with myoclonic seizures in infants and children (severe myoclonic epilepsy and myoclonic-astatic epilepsy).

Guerrini R, Aicardi J.

J Clin Neurophysiol. 2003 Nov-Dec;20(6):449-61. Review.

PMID:
14734934
[PubMed - indexed for MEDLINE]
12.

"Severe myoclonic epilepsy in infancy". Relevance for the clinician of severe epilepsy starting in infancy.

Ceulemans B, Cras P.

Acta Neurol Belg. 2004 Sep;104(3):95-9. Review.

PMID:
15508261
[PubMed - indexed for MEDLINE]
13.

Severe epilepsy syndromes of early childhood: the link between genetics and pathophysiology with a focus on SCN1A mutations.

Stafstrom CE.

J Child Neurol. 2009 Aug;24(8 Suppl):15S-23S. doi: 10.1177/0883073809338152. Review.

PMID:
19666879
[PubMed - indexed for MEDLINE]
14.

[Dravet syndrome as a cause of epilepsy and learning disability].

Lund C, Bremer A, Lossius MI, Selmer KK, Brodtkorb E, Nakken KO.

Tidsskr Nor Laegeforen. 2012 Jan 10;132(1):44-7. doi: 10.4045/tidsskr.11.0539. Review. Norwegian.

PMID:
22240828
[PubMed - indexed for MEDLINE]
Free Article
15.

Molecular and cellular basis: insights from experimental models of Dravet syndrome.

Yamakawa K.

Epilepsia. 2011 Apr;52 Suppl 2:70-1. doi: 10.1111/j.1528-1167.2011.03006.x. Review.

PMID:
21463284
[PubMed - indexed for MEDLINE]
16.

Neuroimaging and neuropathology of Dravet syndrome.

Guerrini R, Striano P, Catarino C, Sisodiya SM.

Epilepsia. 2011 Apr;52 Suppl 2:30-4. doi: 10.1111/j.1528-1167.2011.02998.x. Review.

PMID:
21463276
[PubMed - indexed for MEDLINE]
17.

Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome).

Scheffer IE, Wallace R, Mulley JC, Berkovic SF.

Brain Dev. 2001 Nov;23(7):732-5. Review.

PMID:
11701287
[PubMed - indexed for MEDLINE]
18.

SCN1A mutations in Dravet syndrome: impact of interneuron dysfunction on neural networks and cognitive outcome.

Bender AC, Morse RP, Scott RC, Holmes GL, Lenck-Santini PP.

Epilepsy Behav. 2012 Mar;23(3):177-86. doi: 10.1016/j.yebeh.2011.11.022. Epub 2012 Feb 16. Review.

PMID:
22341965
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Debate: Does genetic information in humans help us treat patients? PRO--genetic information in humans helps us treat patients. CON--genetic information does not help at all.

Delgado-Escueta AV, Bourgeois BF.

Epilepsia. 2008 Dec;49 Suppl 9:13-24. doi: 10.1111/j.1528-1167.2008.01922.x. Review.

PMID:
19087113
[PubMed - indexed for MEDLINE]
20.

Clinical spectrum of SCN1A mutations.

Gambardella A, Marini C.

Epilepsia. 2009 May;50 Suppl 5:20-3. doi: 10.1111/j.1528-1167.2009.02115.x. Review.

PMID:
19469841
[PubMed - indexed for MEDLINE]

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