These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
4. 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]
5. Genetics of epilepsy: current status and perspectives. Kaneko S; Okada M; Iwasa H; Yamakawa K; Hirose S Neurosci Res; 2002 Sep; 44(1):11-30. PubMed ID: 12204289 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. Impact of our understanding of the genetic aetiology of epilepsy. Gardiner RM J Neurol; 2000 May; 247(5):327-34. PubMed ID: 10896263 [TBL] [Abstract][Full Text] [Related]
8. Monogenic idiopathic epilepsies. Gourfinkel-An I; Baulac S; Nabbout R; Ruberg M; Baulac M; Brice A; LeGuern E Lancet Neurol; 2004 Apr; 3(4):209-18. PubMed ID: 15039033 [TBL] [Abstract][Full Text] [Related]
9. Genetic abnormalities underlying familial epilepsy syndromes. Hirose S; Okada M; Yamakawa K; Sugawara T; Fukuma G; Ito M; Kaneko S; Mitsudome A Brain Dev; 2002 Jun; 24(4):211-22. PubMed ID: 12015163 [TBL] [Abstract][Full Text] [Related]
10. First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene. Baulac S; Huberfeld G; Gourfinkel-An I; Mitropoulou G; Beranger A; Prud'homme JF; Baulac M; Brice A; Bruzzone R; LeGuern E Nat Genet; 2001 May; 28(1):46-8. PubMed ID: 11326274 [TBL] [Abstract][Full Text] [Related]
11. [Epilepsy and genetics]. Picard F Rev Med Suisse Romande; 2003 May; 123(5):317-21. PubMed ID: 15095716 [TBL] [Abstract][Full Text] [Related]
15. [Recent insights into the implication of ion channels in familial forms of epilepsies associated or non associated to febrile convulsions]. Gourfinkel-An I; Baulac S; Nabbout R; Brice A; Baulac M; Leguern E Rev Neurol (Paris); 2004 May; 160(5 Pt 2):S90-7. PubMed ID: 15269666 [TBL] [Abstract][Full Text] [Related]
16. 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 Nat Genet; 1995 May; 10(1):117-8. PubMed ID: 7647781 [TBL] [Abstract][Full Text] [Related]
17. Ion channel defects in idiopathic epilepsies. Lerche H; Weber YG; Jurkat-Rott K; Lehmann-Horn F Curr Pharm Des; 2005; 11(21):2737-52. PubMed ID: 16101452 [TBL] [Abstract][Full Text] [Related]