These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
229 related articles for article (PubMed ID: 11701287)
1. 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. PubMed ID: 11701287 [TBL] [Abstract][Full Text] [Related]
2. Absence of mutations in major GEFS+ genes in myoclonic astatic epilepsy. Nabbout R; Kozlovski A; Gennaro E; Bahi-Buisson N; Zara F; Chiron C; Bianchi A; Brice A; Leguern E; Dulac O Epilepsy Res; 2003 Oct; 56(2-3):127-33. PubMed ID: 14642997 [TBL] [Abstract][Full Text] [Related]
3. 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]
6. Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities. Marini C; Mei D; Temudo T; Ferrari AR; Buti D; Dravet C; Dias AI; Moreira A; Calado E; Seri S; Neville B; Narbona J; Reid E; Michelucci R; Sicca F; Cross HJ; Guerrini R Epilepsia; 2007 Sep; 48(9):1678-1685. PubMed ID: 17561957 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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; 63(2):329-34. PubMed ID: 15277629 [TBL] [Abstract][Full Text] [Related]
9. SCN1A mutation analysis in myoclonic astatic epilepsy and severe idiopathic generalized epilepsy of infancy with generalized tonic-clonic seizures. Ebach K; Joos H; Doose H; Stephani U; Kurlemann G; Fiedler B; Hahn A; Hauser E; Hundt K; Holthausen H; Müller U; Neubauer BA Neuropediatrics; 2005 Jun; 36(3):210-3. PubMed ID: 15944908 [TBL] [Abstract][Full Text] [Related]
10. Generalized epilepsy with febrile seizures plus and severe myoclonic epilepsy in infancy: a case report of two Italian families. Veggiotti P; Cardinali S; Montalenti E; Gatti A; Lanzi G Epileptic Disord; 2001; 3(1):29-32. PubMed ID: 11313220 [TBL] [Abstract][Full Text] [Related]
16. [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]
17. [Clinical features and SCN1A gene mutation analysis of severe myoclonic epilepsy of infancy]. Zhang YH; Sun HH; Liu XY; Ma XW; Yang ZX; Xiong H; Qin J; Lin Q; Wu XR Zhonghua Er Ke Za Zhi; 2008 Oct; 46(10):769-73. PubMed ID: 19099883 [TBL] [Abstract][Full Text] [Related]