208 related articles for article (PubMed ID: 12861510)
1. [Severe myoclonic epilepsy in infancy. Clinical and paraclinical aspects].
Martínez-Bermejo A; López-Martín V; Arcas J; Tendero A; Roche Herrero MC; Merino M
Rev Neurol; 2003 Jul 1-15; 37(1):55-9. PubMed ID: 12861510
[TBL] [Abstract][Full Text] [Related]
2. [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; 61(11-12):402-8. PubMed ID: 19070316
[TBL] [Abstract][Full Text] [Related]
3. [Severe myoclonic epilepsy in infancy (Dravet's syndrome). Its nosological characteristics and therapeutic aspects].
Nieto Barrera M; Candau Fernandez Mensaque R; Nieto Jiménez M
Rev Neurol; 2003 Jul 1-15; 37(1):64-8. PubMed ID: 12861512
[TBL] [Abstract][Full Text] [Related]
4. 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. PubMed ID: 15087100
[TBL] [Abstract][Full Text] [Related]
5. "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. PubMed ID: 15508261
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 16806826
[TBL] [Abstract][Full Text] [Related]
7. A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures.
Kimura K; Sugawara T; Mazaki-Miyazaki E; Hoshino K; Nomura Y; Tateno A; Hachimori K; Yamakawa K; Segawa M
Brain Dev; 2005 Sep; 27(6):424-30. PubMed ID: 16122630
[TBL] [Abstract][Full Text] [Related]
8. Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.
Striano P; Mancardi MM; Biancheri R; Madia F; Gennaro E; Paravidino R; Beccaria F; Capovilla G; Dalla Bernardina B; Darra F; Elia M; Giordano L; Gobbi G; Granata T; Ragona F; Guerrini R; Marini C; Mei D; Longaretti F; Romeo A; Siri L; Specchio N; Vigevano F; Striano S; Tortora F; Rossi A; Minetti C; Dravet C; Gaggero R; Zara F
Epilepsia; 2007 Jun; 48(6):1092-6. PubMed ID: 17381446
[TBL] [Abstract][Full Text] [Related]
9. Severe myoclonic epilepsy of infants (Dravet syndrome): natural history and neuropsychological findings.
Wolff M; Cassé-Perrot C; Dravet C
Epilepsia; 2006; 47 Suppl 2():45-8. PubMed ID: 17105460
[TBL] [Abstract][Full Text] [Related]
10. Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.
Zucca C; Redaelli F; Epifanio R; Zanotta N; Romeo A; Lodi M; Veggiotti P; Airoldi G; Panzeri C; Romaniello R; De Polo G; Bonanni P; Cardinali S; Baschirotto C; Martorell L; Borgatti R; Bresolin N; Bassi MT
Arch Neurol; 2008 Apr; 65(4):489-94. PubMed ID: 18413471
[TBL] [Abstract][Full Text] [Related]
11. 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. PubMed ID: 19854600
[TBL] [Abstract][Full Text] [Related]
12. [Severe myoclonic epilepsy in infancy (Dravet's syndrome). Some genetic aspects].
Herranz JL
Rev Neurol; 2003 Jul 1-15; 37(1):60-3. PubMed ID: 12861511
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 12754708
[TBL] [Abstract][Full Text] [Related]
14. [Myoclonic epilepsies in infancy].
Palencia R
Rev Neurol; 2000 Jun; 30 Suppl 1():S15-24. PubMed ID: 10904965
[TBL] [Abstract][Full Text] [Related]
15. Clinical evaluation and diagnosis of severe epilepsy syndromes of early childhood.
Zupanc ML
J Child Neurol; 2009 Aug; 24(8 Suppl):6S-14S. PubMed ID: 19666878
[TBL] [Abstract][Full Text] [Related]
16. Symptomatic epilepsies imitating idiopathic generalized epilepsies.
Oguni H
Epilepsia; 2005; 46 Suppl 9():84-90. PubMed ID: 16302880
[TBL] [Abstract][Full Text] [Related]
17. [Reflex myoclonic epilepsy in infancy: a new reflex epilepsy syndrome or a variant of benign myoclonic epilepsy in infancy].
Caraballo R; Cassar L; Monges S; Yepez I; Galicchio S; Cersósimo R; Fejerman N
Rev Neurol; 2003 Mar 1-15; 36(5):429-32. PubMed ID: 12640595
[TBL] [Abstract][Full Text] [Related]
18. The core Dravet syndrome phenotype.
Dravet C
Epilepsia; 2011 Apr; 52 Suppl 2():3-9. PubMed ID: 21463272
[TBL] [Abstract][Full Text] [Related]
19. Dravet syndrome: from electroclinical characteristics to molecular biology.
Arzimanoglou A
Epilepsia; 2009 Sep; 50 Suppl 8():3-9. PubMed ID: 19702726
[TBL] [Abstract][Full Text] [Related]
20. The natural history of myoclonic astatic epilepsy (Doose syndrome) and Lennox-Gastaut syndrome.
Stephani U
Epilepsia; 2006; 47 Suppl 2():53-5. PubMed ID: 17105462
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
