Similar articles for PMID: 7647781

Year	Number of Results
1910	1
1950	2
1986	1
1987	1
1989	1
1991	3
1992	6
1993	6
1994	6
1995	7
1996	7
1997	8
1998	8
1999	11
2000	11
2001	3
2002	10
2003	9
2004	4
2005	7
2006	2
2007	5
2008	5
2009	2
2010	6
2011	7
2012	9
2013	5
2014	3
2015	3
2016	2
2018	2
2019	2
2020	3
2021	2
2022	2
2024	0

1

Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2.

Phillips HA, Scheffer IE, Berkovic SF, Hollway GE, Sutherland GR, Mulley JC. Phillips HA, et al. Nat Genet. 1995 May;10(1):117-8. doi: 10.1038/ng0595-117. Nat Genet. 1995. PMID: 7647781

2

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. Steinlein OK, et al. Nat Genet. 1995 Oct;11(2):201-3. doi: 10.1038/ng1095-201. Nat Genet. 1995. PMID: 7550350

3

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. De Marco EV, et al. Epilepsy Res. 2007 Apr;74(1):70-3. doi: 10.1016/j.eplepsyres.2006.12.006. Epub 2007 Feb 26. Epilepsy Res. 2007. PMID: 17324557

4

Gene defects in idiopathic epilepsy.

Steinlein OK. Steinlein OK. Rev Neurol (Paris). 1999 Jul;155(6-7):450-3. Rev Neurol (Paris). 1999. PMID: 10472657 Review.

5

Evidence for a fourth locus for autosomal dominant nocturnal frontal lobe epilepsy.

Combi R, Dalprà L, Malcovati M, Oldani A, Tenchini ML, Ferini-Strambi L. Combi R, et al. Brain Res Bull. 2004 Jun 30;63(5):353-9. doi: 10.1016/j.brainresbull.2003.12.007. Brain Res Bull. 2004. PMID: 15245761

6

[Autosomal dominant nocturnal frontal lobe epilepsy].

Thomas P, Picard F, Hirsch E, Chatel M, Marescaux C. Thomas P, et al. Rev Neurol (Paris). 1998 Apr;154(3):228-35. Rev Neurol (Paris). 1998. PMID: 9773047 French.

7

[Autosomal dominant nocturnal frontal lobe epilepsy: the syndrome].

Picard F, Chauvel P. Picard F, et al. Rev Neurol (Paris). 1999 Jul;155(6-7):445-9. Rev Neurol (Paris). 1999. PMID: 10472656 Review. French.

8

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.

Charlier C, Singh NA, Ryan SG, Lewis TB, Reus BE, Leach RJ, Leppert M. Charlier C, et al. Nat Genet. 1998 Jan;18(1):53-5. doi: 10.1038/ng0198-53. Nat Genet. 1998. PMID: 9425900

9

Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12.

Berkovic SF, Serratosa JM, Phillips HA, Xiong L, Andermann E, Díaz-Otero F, Gómez-Garre P, Martín M, Fernández-Bullido Y, Andermann F, Lopes-Cendes I, Dubeau F, Desbiens R, Scheffer IE, Wallace RH, Mulley JC, Pandolfo M. Berkovic SF, et al. Epilepsia. 2004 Sep;45(9):1054-60. doi: 10.1111/j.0013-9580.2004.30502.x. Epilepsia. 2004. PMID: 15329069 Free article.

10

[Epilepsy and genetics].

Picard F. Picard F. Rev Med Suisse Romande. 2003 May;123(5):317-21. Rev Med Suisse Romande. 2003. PMID: 15095716 Review. French.

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