275 related articles for article (PubMed ID: 15715999)
21. Variable neurologic phenotype in a GEFS+ family with a novel mutation in SCN1A.
Mahoney K; Moore SJ; Buckley D; Alam M; Parfrey P; Penney S; Merner N; Hodgkinson K; Young TL
Seizure; 2009 Sep; 18(7):492-7. PubMed ID: 19464195
[TBL] [Abstract][Full Text] [Related]
22. Genotype-phenotype associations in SCN1A-related epilepsies.
Zuberi SM; Brunklaus A; Birch R; Reavey E; Duncan J; Forbes GH
Neurology; 2011 Feb; 76(7):594-600. PubMed ID: 21248271
[TBL] [Abstract][Full Text] [Related]
23. Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus.
Annesi G; Gambardella A; Carrideo S; Incorpora G; Labate A; Pasqua AA; Civitelli D; Polizzi A; Annesi F; Spadafora P; Tarantino P; CirĂ² Candiano IC; Romeo N; De Marco EV; Ventura P; LePiane E; Zappia M; Aguglia U; Pavone L; Quattrone A
Epilepsia; 2003 Sep; 44(9):1257-8. PubMed ID: 12919402
[No Abstract] [Full Text] [Related]
24. 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]
25. Variable epilepsy phenotypes associated with a familial intragenic deletion of the SCN1A gene.
Guerrini R; Cellini E; Mei D; Metitieri T; Petrelli C; Pucatti D; Marini C; Zamponi N
Epilepsia; 2010 Dec; 51(12):2474-7. PubMed ID: 21204810
[TBL] [Abstract][Full Text] [Related]
26. Clinical spectrum of SCN1A mutations.
Gambardella A; Marini C
Epilepsia; 2009 May; 50 Suppl 5():20-3. PubMed ID: 19469841
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: associated with loss of function of Na(v) 1.1.
Liao WP; Shi YW; Long YS; Zeng Y; Li T; Yu MJ; Su T; Deng P; Lei ZG; Xu SJ; Deng WY; Liu XR; Sun WW; Yi YH; Xu ZC; Duan S
Epilepsia; 2010 Sep; 51(9):1669-78. PubMed ID: 20550552
[TBL] [Abstract][Full Text] [Related]
29. GEFS+ where focal seizures evolve from generalized spike wave: video-EEG study of two children.
Deng YH; Berkovic SF; Scheffer IE
Epileptic Disord; 2007 Sep; 9(3):307-14. PubMed ID: 17884755
[TBL] [Abstract][Full Text] [Related]
30. Febrile seizures, genetic (generalized) epilepsy with febrile seizures plus, and Dravet's syndrome.
Scanlon A; Cook SS
J Spec Pediatr Nurs; 2010 Apr; 15(2):154-9. PubMed ID: 20367785
[TBL] [Abstract][Full Text] [Related]
31. A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family.
Cui X; Zeng F; Liu Y; Zhang J; Archacki S; Zhan T; Du R; Tang Z; Liu J; Wang QK; Liu M
Neurosci Lett; 2011 Sep; 503(1):27-30. PubMed ID: 21843600
[TBL] [Abstract][Full Text] [Related]
32. Autism in several members of a family with generalized epilepsy with febrile seizures plus.
Dixon-Salazar TJ; Keeler LC; Trauner DA; Gleeson JG
J Child Neurol; 2004 Aug; 19(8):597-603. PubMed ID: 15605469
[TBL] [Abstract][Full Text] [Related]
33. Patients with a sodium channel alpha 1 gene mutation show wide phenotypic variation.
Osaka H; Ogiwara I; Mazaki E; Okamura N; Yamashita S; Iai M; Yamada M; Kurosawa K; Iwamoto H; Yasui-Furukori N; Kaneko S; Fujiwara T; Inoue Y; Yamakawa K
Epilepsy Res; 2007 Jun; 75(1):46-51. PubMed ID: 17507202
[TBL] [Abstract][Full Text] [Related]
34. A novel locus for generalized epilepsy with febrile seizures plus in French families.
Baulac S; Gourfinkel-An I; Couarch P; Depienne C; Kaminska A; Dulac O; Baulac M; LeGuern E; Nabbout R
Arch Neurol; 2008 Jul; 65(7):943-51. PubMed ID: 18625863
[TBL] [Abstract][Full Text] [Related]
35. Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutation.
Hindocha N; Nashef L; Elmslie F; Birch R; Zuberi S; Al-Chalabi A; Crotti L; Schwartz PJ; Makoff A
Epilepsia; 2008 Feb; 49(2):360-5. PubMed ID: 18251839
[No Abstract] [Full Text] [Related]
36. Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations.
Bonanni P; Malcarne M; Moro F; Veggiotti P; Buti D; Ferrari AR; Parrini E; Mei D; Volzone A; Zara F; Heron SE; Bordo L; Marini C; Guerrini R
Epilepsia; 2004 Feb; 45(2):149-58. PubMed ID: 14738422
[TBL] [Abstract][Full Text] [Related]
37. Partial and generalized epilepsy with febrile seizures plus and a novel SCN1A mutation.
Abou-Khalil B; Ge Q; Desai R; Ryther R; Bazyk A; Bailey R; Haines JL; Sutcliffe JS; George AL
Neurology; 2001 Dec; 57(12):2265-72. PubMed ID: 11756608
[TBL] [Abstract][Full Text] [Related]
38. SCN1A, SCN1B, and GABRG2 gene mutation analysis in Chinese families with generalized epilepsy with febrile seizures plus.
Sun H; Zhang Y; Liang J; Liu X; Ma X; Wu H; Xu K; Qin J; Qi Y; Wu X
J Hum Genet; 2008; 53(8):769-774. PubMed ID: 18566737
[TBL] [Abstract][Full Text] [Related]
39. Does genotype determine phenotype? Sodium channel mutations in Dravet syndrome and GEFS+.
Scheffer IE
Neurology; 2011 Feb; 76(7):588-9. PubMed ID: 21248272
[No Abstract] [Full Text] [Related]
40. Two novel mutations in SCN1A gene in Iranian patients with epilepsy.
Ebrahimi A; Houshmand M; Tonekaboni SH; Fallah Mahboob Passand MS; Zainali S; Moghadasi M
Arch Med Res; 2010 Apr; 41(3):207-14. PubMed ID: 20682179
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]