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Items: 1 to 20 of 21

1.

Sudden death in epilepsy: of mice and men.

Friedman D, Chyou J, Devinsky O.

J Clin Invest. 2013 Apr;123(4):1415-6. doi: 10.1172/JCI67759. Epub 2013 Mar 25.

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
3.

Dravet syndrome (severe myoclonic epilepsy in infancy).

Dravet C, Oguni H.

Handb Clin Neurol. 2013;111:627-33. doi: 10.1016/B978-0-444-52891-9.00065-8. Review.

PMID:
23622210
4.

[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.

5.

Dravet syndrome: the long-term outcome.

Genton P, Velizarova R, Dravet C.

Epilepsia. 2011 Apr;52 Suppl 2:44-9. doi: 10.1111/j.1528-1167.2011.03001.x. Review.

6.
7.

Myoclonic-astatic epilepsy.

Doose H.

Epilepsy Res Suppl. 1992;6:163-8. Review.

PMID:
1418479
8.

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.

9.

Dravet syndrome, what is new?

Al-Baradie RS.

Neurosciences (Riyadh). 2013 Jan;18(1):11-7. Review.

PMID:
23291792
10.

"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
11.
12.

The ketogenic diet in Dravet syndrome.

Laux L, Blackford R.

J Child Neurol. 2013 Aug;28(8):1041-4. doi: 10.1177/0883073813487599. Epub 2013 May 7. Review.

PMID:
23653425
13.

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
14.

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.

15.

[Myoclonias and epilepsy].

Salas-Puig J.

Rev Neurol. 2001 Mar 16-31;32(6):568-73. Review. Spanish.

PMID:
11353998
16.

Mortality in Dravet syndrome: A review.

Shmuely S, Sisodiya SM, Gunning WB, Sander JW, Thijs RD.

Epilepsy Behav. 2016 Nov;64(Pt A):69-74. doi: 10.1016/j.yebeh.2016.09.007. Epub 2016 Oct 11. Review.

17.

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.

18.

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
19.
20.

Diagnosis and long-term course of Dravet syndrome.

Scheffer IE.

Eur J Paediatr Neurol. 2012 Sep;16 Suppl 1:S5-8. doi: 10.1016/j.ejpn.2012.04.007. Epub 2012 Jun 16. Review.

PMID:
22704920

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