659 related articles for article (PubMed ID: 15264690)
1. [Genetic background of epilepsies].
Kelemen A; Szucs A; Rásonyi G; Janszky J; Holló A; Halász P
Ideggyogy Sz; 2004 May; 57(5-6):141-51. PubMed ID: 15264690
[TBL] [Abstract][Full Text] [Related]
2. Genes and mutations in idiopathic epilepsy.
Steinlein OK
Am J Med Genet; 2001; 106(2):139-45. PubMed ID: 11579434
[TBL] [Abstract][Full Text] [Related]
3. Genetics of idiopathic epilepsies.
Hirose S; Mitsudome A; Okada M; Kaneko S;
Epilepsia; 2005; 46 Suppl 1():38-43. PubMed ID: 15816978
[TBL] [Abstract][Full Text] [Related]
4. Channelopathies can cause epilepsy in man.
Steinlein OK
Eur J Pain; 2002; 6 Suppl A():27-34. PubMed ID: 11888238
[TBL] [Abstract][Full Text] [Related]
5. Gene defects in idiopathic epilepsy.
Steinlein OK
Rev Neurol (Paris); 1999 Jul; 155(6-7):450-3. PubMed ID: 10472657
[TBL] [Abstract][Full Text] [Related]
6. Ion channels and epilepsy.
Lerche H; Jurkat-Rott K; Lehmann-Horn F
Am J Med Genet; 2001; 106(2):146-59. PubMed ID: 11579435
[TBL] [Abstract][Full Text] [Related]
7. [Genetic approach to the pathogeneses of epilepsy].
Hirose S
Rinsho Shinkeigaku; 2004 Nov; 44(11):975-8. PubMed ID: 15651347
[TBL] [Abstract][Full Text] [Related]
8. KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum.
Singh NA; Westenskow P; Charlier C; Pappas C; Leslie J; Dillon J; Anderson VE; Sanguinetti MC; Leppert MF;
Brain; 2003 Dec; 126(Pt 12):2726-37. PubMed ID: 14534157
[TBL] [Abstract][Full Text] [Related]
9. [Benign familial neonatal convulsions: a model of idiopathic epilepsy].
Hirsch E; de Saint-Martin A; Marescaux C
Rev Neurol (Paris); 1999 Jul; 155(6-7):463-7. PubMed ID: 10472660
[TBL] [Abstract][Full Text] [Related]
10. [Ion channels and epilepsy].
Armijo JA; de las Cuevas I; Adín J
Rev Neurol; 2000 Jun; 30 Suppl 1():S25-41. PubMed ID: 10904966
[TBL] [Abstract][Full Text] [Related]
11. Neonatal epilepsy syndromes and GEFS+: mechanistic considerations.
Burgess DL
Epilepsia; 2005; 46 Suppl 10():51-8. PubMed ID: 16359473
[TBL] [Abstract][Full Text] [Related]
12. Neonatal epilepsy syndromes and generalized epilepsy with febrile seizures plus (GEFS+).
Scheffer IE; Harkin LA; Dibbens LM; Mulley JC; Berkovic SF
Epilepsia; 2005; 46 Suppl 10():41-7. PubMed ID: 16359471
[No Abstract] [Full Text] [Related]
13. A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family.
Lee WL; Biervert C; Hallmann K; Tay A; Dean JC; Steinlein OK
Neuropediatrics; 2000 Feb; 31(1):9-12. PubMed ID: 10774989
[TBL] [Abstract][Full Text] [Related]
14. [Epilepsy and genetics].
Picard F
Rev Med Suisse Romande; 2003 May; 123(5):317-21. PubMed ID: 15095716
[TBL] [Abstract][Full Text] [Related]
15. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.
Singh NA; Charlier C; Stauffer D; DuPont BR; Leach RJ; Melis R; Ronen GM; Bjerre I; Quattlebaum T; Murphy JV; McHarg ML; Gagnon D; Rosales TO; Peiffer A; Anderson VE; Leppert M
Nat Genet; 1998 Jan; 18(1):25-9. PubMed ID: 9425895
[TBL] [Abstract][Full Text] [Related]
16. Sodium and potassium channel dysfunctions in rare and common idiopathic epilepsy syndromes.
Hahn A; Neubauer BA
Brain Dev; 2009 Aug; 31(7):515-20. PubMed ID: 19464834
[TBL] [Abstract][Full Text] [Related]
17. Complete loss of the cytoplasmic carboxyl terminus of the KCNQ2 potassium channel: a novel mutation in a large Czech pedigree with benign neonatal convulsions or other epileptic phenotypes.
Pereira S; Roll P; Krizova J; Genton P; Brazdil M; Kuba R; Cau P; Rektor I; Szepetowski P
Epilepsia; 2004 Apr; 45(4):384-90. PubMed ID: 15030501
[TBL] [Abstract][Full Text] [Related]
18. Idiopathic epilepsies with a monogenic mode of inheritance.
Steinlein OK
Epilepsia; 1999; 40 Suppl 3():9-11. PubMed ID: 10446744
[TBL] [Abstract][Full Text] [Related]
19. Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy.
Schroeder BC; Kubisch C; Stein V; Jentsch TJ
Nature; 1998 Dec; 396(6712):687-90. PubMed ID: 9872318
[TBL] [Abstract][Full Text] [Related]
20. [Genetics of epilepsy].
Hirose S
Seishin Shinkeigaku Zasshi; 2003; 105(4):407-12. PubMed ID: 12806902
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]