206 related articles for article (PubMed ID: 25770198)
1. 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]
2.
Villa C; Colombo G; Meneghini S; Gotti C; Moretti M; Ferini-Strambi L; Chisci E; Giovannoni R; Becchetti A; Combi R
Front Mol Neurosci; 2019; 12():17. PubMed ID: 30809122
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
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. [Generation of epilepsy animal model bearing a genetic abnormality identified in autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) of humans].
Okada M
Nihon Shinkei Seishin Yakurigaku Zasshi; 2010 Feb; 30(1):9-14. PubMed ID: 20297737
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. Autosomal dominant nocturnal frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome.
Oldani A; Zucconi M; Asselta R; Modugno M; Bonati MT; Dalprà L; Malcovati M; Tenchini ML; Smirne S; Ferini-Strambi L
Brain; 1998 Feb; 121 ( Pt 2)():205-23. PubMed ID: 9549500
[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. 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]
11. 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]
12. Spontaneous epileptic seizures in transgenic rats harboring a human ADNFLE missense mutation in the β2-subunit of the nicotinic acetylcholine receptor.
Shiba Y; Mori F; Yamada J; Migita K; Nikaido Y; Wakabayashi K; Kaneko S; Okada M; Hirose S; Ueno S
Neurosci Res; 2015 Nov; 100():46-54. PubMed ID: 26091610
[TBL] [Abstract][Full Text] [Related]
13. 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]
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. The role of the nicotinic acetylcholine receptors in sleep-related epilepsy.
Marini C; Guerrini R
Biochem Pharmacol; 2007 Oct; 74(8):1308-14. PubMed ID: 17662253
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Human nocturnal frontal lobe epilepsy: pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor beta-subunit mutations outside the ion channel pore.
Hoda JC; Gu W; Friedli M; Phillips HA; Bertrand S; Antonarakis SE; Goudie D; Roberts R; Scheffer IE; Marini C; Patel J; Berkovic SF; Mulley JC; Steinlein OK; Bertrand D
Mol Pharmacol; 2008 Aug; 74(2):379-91. PubMed ID: 18456869
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Mutation of CHRNA2 in a family with benign familial infantile seizures: Potential role of nicotinic acetylcholine receptor in various phenotypes of epilepsy.
Trivisano M; Terracciano A; Milano T; Cappelletti S; Pietrafusa N; Bertini ES; Vigevano F; Specchio N
Epilepsia; 2015 May; 56(5):e53-7. PubMed ID: 25847220
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
