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Results: 1 to 20 of 35

Related Articles by Review for PubMed (Select 21719429)

1.

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.

Catarino CB, Liu JY, Liagkouras I, Gibbons VS, Labrum RW, Ellis R, Woodward C, Davis MB, Smith SJ, Cross JH, Appleton RE, Yendle SC, McMahon JM, Bellows ST, Jacques TS, Zuberi SM, Koepp MJ, Martinian L, Scheffer IE, Thom M, Sisodiya SM.

Brain. 2011 Oct;134(Pt 10):2982-3010. doi: 10.1093/brain/awr129. Epub 2011 Jun 29.

2.

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
3.

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
4.

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
5.

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
6.

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.

7.

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
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
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
10.

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
11.

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
12.

Dravet syndrome: a genetic epileptic disorder.

Akiyama M, Kobayashi K, Ohtsuka Y.

Acta Med Okayama. 2012;66(5):369-76. Review.

13.

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
14.

Dravet syndrome: the main issues.

Guerrini R.

Eur J Paediatr Neurol. 2012 Sep;16 Suppl 1:S1-4. doi: 10.1016/j.ejpn.2012.04.006. Epub 2012 Jun 15. Review.

PMID:
22705271
15.

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
16.

Insights into pathophysiology and therapy from a mouse model of Dravet syndrome.

Oakley JC, Kalume F, Catterall WA.

Epilepsia. 2011 Apr;52 Suppl 2:59-61. doi: 10.1111/j.1528-1167.2011.03004.x. Review.

17.

Molecular basis of severe myoclonic epilepsy in infancy.

Yamakawa K.

Brain Dev. 2009 May;31(5):401-4. doi: 10.1016/j.braindev.2008.11.015. Epub 2009 Feb 8. Review.

PMID:
19203854
18.

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
19.

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
20.

Dravet syndrome history.

Dravet C.

Dev Med Child Neurol. 2011 Apr;53 Suppl 2:1-6. doi: 10.1111/j.1469-8749.2011.03964.x. Review.

PMID:
21504424
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