141 related articles for article (PubMed ID: 21287502)
1. [Mutational analysis of CHRNB2 and CHRNA2 genes in southern Chinese population with autosomal dominant nocturnal frontal lobe epilepsy].
Chen ZH; Zhai QX; Gui J; Zhang YX; Guo YX; Ding J; Hao Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Feb; 28(1):14-8. PubMed ID: 21287502
[TBL] [Abstract][Full Text] [Related]
2. Mutational analysis of CHRNB2, CHRNA2 and CHRNA4 genes in Chinese population with autosomal dominant nocturnal frontal lobe epilepsy.
Chen Z; Wang L; Wang C; Chen Q; Zhai Q; Guo Y; Zhang Y
Int J Clin Exp Med; 2015; 8(6):9063-70. PubMed ID: 26309560
[TBL] [Abstract][Full Text] [Related]
3. [Clinical features and mutation analysis of CHRNA4 gene for families and sporadic cases affected with autosomal dominant nocturnal frontal lobe epilepsy].
Zhai QX; Wang C; Chen Q; Guo YX; Chen ZH; Zhang YX; Gui J; Tang ZH; Zhuo MQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Dec; 30(6):662-5. PubMed ID: 24327142
[TBL] [Abstract][Full Text] [Related]
4. The identification of a novel mutation of nicotinic acetylcholine receptor gene CHRNB2 in a Chinese patient: Its possible implication in non-familial nocturnal frontal lobe epilepsy.
Liu H; Lu C; Li Z; Zhou S; Li X; Ji L; Lu Q; Lv R; Wu L; Ma X
Epilepsy Res; 2011 Jun; 95(1-2):94-9. PubMed ID: 21497487
[TBL] [Abstract][Full Text] [Related]
5. A major role of the nicotinic acetylcholine receptor gene CHRNA2 in autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) is unlikely.
Gu W; Bertrand D; Steinlein OK
Neurosci Lett; 2007 Jul; 422(1):74-6. PubMed ID: 17602836
[TBL] [Abstract][Full Text] [Related]
6. Nocturnal frontal lobe epilepsy with paroxysmal arousals due to CHRNA2 loss of function.
Conti V; Aracri P; Chiti L; Brusco S; Mari F; Marini C; Albanese M; Marchi A; Liguori C; Placidi F; Romigi A; Becchetti A; Guerrini R
Neurology; 2015 Apr; 84(15):1520-8. PubMed ID: 25770198
[TBL] [Abstract][Full Text] [Related]
7. A novel mutation of the nicotinic acetylcholine receptor gene CHRNA4 in sporadic nocturnal frontal lobe epilepsy.
Chen Y; Wu L; Fang Y; He Z; Peng B; Shen Y; Xu Q
Epilepsy Res; 2009 Feb; 83(2-3):152-6. PubMed ID: 19058950
[TBL] [Abstract][Full Text] [Related]
8. Mutational analysis of nicotinic acetylcholine receptor beta2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsy.
Duga S; Asselta R; Bonati MT; Malcovati M; Dalprà L; Oldani A; Zucconi M; Ferini-Strambi L; Tenchini ML
Epilepsia; 2002 Apr; 43(4):362-4. PubMed ID: 11952766
[TBL] [Abstract][Full Text] [Related]
9. Autosomal dominant nocturnal frontal lobe epilepsy with a mutation in the CHRNB2 gene.
Díaz-Otero F; Quesada M; Morales-Corraliza J; Martínez-Parra C; Gómez-Garre P; Serratosa JM
Epilepsia; 2008 Mar; 49(3):516-20. PubMed ID: 17900292
[TBL] [Abstract][Full Text] [Related]
10. A novel mutation of the nicotinic acetylcholine receptor gene CHRNA4 in a Chinese patient with non-familial nocturnal frontal lobe epilepsy.
Wang MY; Liu XZ; Wang J; Wu LW
Epilepsy Res; 2014 Dec; 108(10):1927-31. PubMed ID: 25282705
[TBL] [Abstract][Full Text] [Related]
11. Further evidence of genetic heterogeneity in families with autosomal dominant nocturnal frontal lobe epilepsy.
De Marco EV; Gambardella A; Annesi F; Labate A; Carrideo S; Forabosco P; Civitelli D; Candiano IC; Tarantino P; Annesi G; Quattrone A
Epilepsy Res; 2007 Apr; 74(1):70-3. PubMed ID: 17324557
[TBL] [Abstract][Full Text] [Related]
12. CHRNA2 mutations are rare in the NFLE population: evaluation of a large cohort of Italian patients.
Combi R; Ferini-Strambi L; Tenchini ML
Sleep Med; 2009 Jan; 10(1):139-42. PubMed ID: 18226955
[TBL] [Abstract][Full Text] [Related]
13. Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated families.
Bonati MT; Combi R; Asselta R; Duga S; Malcovati M; Oldani A; Zucconi M; Ferini-Strambi L; Dalprà L; Tenchini ML
J Neurol; 2002 Aug; 249(8):967-74. PubMed ID: 12195439
[TBL] [Abstract][Full Text] [Related]
14. Pleiotropic functional effects of the first epilepsy-associated mutation in the human CHRNA2 gene.
Hoda JC; Wanischeck M; Bertrand D; Steinlein OK
FEBS Lett; 2009 May; 583(10):1599-604. PubMed ID: 19383498
[TBL] [Abstract][Full Text] [Related]
15. Autosomal dominant nocturnal frontal lobe epilepsy: a genotypic comparative study of Japanese and Korean families carrying the CHRNA4 Ser284Leu mutation.
Hwang SK; Makita Y; Kurahashi H; Cho YW; Hirose S
J Hum Genet; 2011 Aug; 56(8):609-12. PubMed ID: 21753767
[TBL] [Abstract][Full Text] [Related]
16. Autosomal dominant nocturnal frontal lobe epilepsy--a critical overview.
Combi R; Dalprà L; Tenchini ML; Ferini-Strambi L
J Neurol; 2004 Aug; 251(8):923-34. PubMed ID: 15316796
[TBL] [Abstract][Full Text] [Related]
17. A case of autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) coexisting with pervasive developmental disorder harboring SCN1A mutation in addition to CHRNB2 mutation.
Sone D; Sugawara T; Sakakibara E; Tomioka Y; Taniguchi G; Murata Y; Watanabe M; Kaneko S
Epilepsy Behav; 2012 Oct; 25(2):192-5. PubMed ID: 23032131
[TBL] [Abstract][Full Text] [Related]
18. A novel mutation of CHRNA4 responsible for autosomal dominant nocturnal frontal lobe epilepsy.
Hirose S; Iwata H; Akiyoshi H; Kobayashi K; Ito M; Wada K; Kaneko S; Mitsudome A
Neurology; 1999 Nov; 53(8):1749-53. PubMed ID: 10563623
[TBL] [Abstract][Full Text] [Related]
19. Electroclinical picture of autosomal dominant nocturnal frontal lobe epilepsy in a Japanese family.
Ito M; Kobayashi K; Fujii T; Okuno T; Hirose S; Iwata H; Mitsudome A; Kaneko S
Epilepsia; 2000 Jan; 41(1):52-8. PubMed ID: 10643924
[TBL] [Abstract][Full Text] [Related]
20. CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy.
Phillips HA; Favre I; Kirkpatrick M; Zuberi SM; Goudie D; Heron SE; Scheffer IE; Sutherland GR; Berkovic SF; Bertrand D; Mulley JC
Am J Hum Genet; 2001 Jan; 68(1):225-31. PubMed ID: 11104662
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
