142 related articles for article (PubMed ID: 25282705)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Rats harboring S284L Chrna4 mutation show attenuation of synaptic and extrasynaptic GABAergic transmission and exhibit the nocturnal frontal lobe epilepsy phenotype.
Zhu G; Okada M; Yoshida S; Ueno S; Mori F; Takahara T; Saito R; Miura Y; Kishi A; Tomiyama M; Sato A; Kojima T; Fukuma G; Wakabayashi K; Hase K; Ohno H; Kijima H; Takano Y; Mitsudome A; Kaneko S; Hirose S
J Neurosci; 2008 Nov; 28(47):12465-76. PubMed ID: 19020039
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Evidence for S284L mutation of the CHRNA4 in a white family with autosomal dominant nocturnal frontal lobe epilepsy.
Rozycka A; Skorupska E; Kostyrko A; Trzeciak WH
Epilepsia; 2003 Aug; 44(8):1113-7. PubMed ID: 12887446
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. 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]
12. 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]
13. 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]
14. A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy.
Steinlein OK; Mulley JC; Propping P; Wallace RH; Phillips HA; Sutherland GR; Scheffer IE; Berkovic SF
Nat Genet; 1995 Oct; 11(2):201-3. PubMed ID: 7550350
[TBL] [Abstract][Full Text] [Related]
15. 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]
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. An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy.
Steinlein OK; Magnusson A; Stoodt J; Bertrand S; Weiland S; Berkovic SF; Nakken KO; Propping P; Bertrand D
Hum Mol Genet; 1997 Jun; 6(6):943-7. PubMed ID: 9175743
[TBL] [Abstract][Full Text] [Related]
18. Autosomal dominant nocturnal frontal lobe epilepsy and mild memory impairment associated with CHRNB2 mutation I312M in the neuronal nicotinic acetylcholine receptor.
Cho YW; Yi SD; Lim JG; Kim DK; Motamedi GK
Epilepsy Behav; 2008 Aug; 13(2):361-5. PubMed ID: 18534914
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]