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Results: 1 to 20 of 77

Related Articles by Review for PubMed (Select 11488881)

1.

Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?

Singh R, Andermann E, Whitehouse WP, Harvey AS, Keene DL, Seni MH, Crossland KM, Andermann F, Berkovic SF, Scheffer IE.

Epilepsia. 2001 Jul;42(7):837-44.

PMID:
11488881
2.

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
3.

[Severe myoclonic epilepsy in infancy (Dravet's syndrome). Some genetic aspects].

Herranz JL.

Rev Neurol. 2003 Jul 1-15;37(1):60-3. Review. Spanish.

4.

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
5.

Effect of localization of missense mutations in SCN1A on epilepsy phenotype severity.

Kanai K, Hirose S, Oguni H, Fukuma G, Shirasaka Y, Miyajima T, Wada K, Iwasa H, Yasumoto S, Matsuo M, Ito M, Mitsudome A, Kaneko S.

Neurology. 2004 Jul 27;63(2):329-34. Review.

PMID:
15277629
6.

Myoclonic-astatic epilepsy.

Doose H.

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

PMID:
1418479
7.
8.

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
9.

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
10.
11.
12.

SCN1A-Related Seizure Disorders .

Miller IO, Sotero de Menezes MA.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2015.
2007 Nov 29 [updated 2014 May 15].

13.

Dissecting the genetic basis of myoclonic-astatic epilepsy.

Tang S, Pal DK.

Epilepsia. 2012 Aug;53(8):1303-13. doi: 10.1111/j.1528-1167.2012.03581.x. Epub 2012 Jul 10. Review.

PMID:
22780699
14.

Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+).

Scheffer IE, Harkin LA, Dibbens LM, Mulley JC, Berkovic SF.

Epilepsia. 2005;46 Suppl 10:41-7. Review. No abstract available.

PMID:
16359471
15.

Gene mapping in the idiopathic generalized epilepsies: juvenile myoclonic epilepsy, childhood absence epilepsy, epilepsy with grand mal seizures, and early childhood myoclonic epilepsy.

Delgado-Escueta AV, Greenberg D, Weissbecker K, Liu A, Treiman L, Sparkes R, Park MS, Barbetti A, Terasaki PI.

Epilepsia. 1990;31 Suppl 3:S19-29. Review.

PMID:
2121470
16.

A practical approach to uncomplicated seizures in children.

McAbee GN, Wark JE.

Am Fam Physician. 2000 Sep 1;62(5):1109-16. Review.

17.

[Epilepsy beginning in the neonatal period and early infancy].

Ruggieri VL.

Rev Neurol. 2004 Aug 1-15;39(3):251-62. Review. Spanish.

18.

Clinical evaluation and diagnosis of severe epilepsy syndromes of early childhood.

Zupanc ML.

J Child Neurol. 2009 Aug;24(8 Suppl):6S-14S. doi: 10.1177/0883073809338151. Review.

PMID:
19666878
19.

Epileptic syndromes in childhood: clinical features, outcomes, and treatment.

Camfield P, Camfield C.

Epilepsia. 2002;43 Suppl 3:27-32. Review.

PMID:
12060004
20.

[Myoclonus and myoclonic epilepsies in childhood].

Nieto-Barrera M.

Rev Neurol. 1999 Feb 1-15;28(3):278-84. Review. Spanish.

PMID:
10714297
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