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.
566 related articles for article (PubMed ID: 9425895)
21. [Progress in molecular genetics of epilepsy]. Tang B; Zhang Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Dec; 19(6):505-7. PubMed ID: 12476426 [TBL] [Abstract][Full Text] [Related]
22. Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions. Volkers L; Rook MB; Das JH; Verbeek NE; Groenewegen WA; van Kempen MJ; Lindhout D; Koeleman BP Neurosci Lett; 2009 Oct; 462(1):24-9. PubMed ID: 19559753 [TBL] [Abstract][Full Text] [Related]
23. 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]
24. M-channels: neurological diseases, neuromodulation, and drug development. Cooper EC; Jan LY Arch Neurol; 2003 Apr; 60(4):496-500. PubMed ID: 12707061 [TBL] [Abstract][Full Text] [Related]
25. Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsions. Biervert C; Steinlein OK Hum Genet; 1999 Mar; 104(3):234-40. PubMed ID: 10323247 [TBL] [Abstract][Full Text] [Related]
26. Neonatal convulsions and epileptic encephalopathy in an Italian family with a missense mutation in the fifth transmembrane region of KCNQ2. Dedek K; Fusco L; Teloy N; Steinlein OK Epilepsy Res; 2003 Apr; 54(1):21-7. PubMed ID: 12742592 [TBL] [Abstract][Full Text] [Related]
27. A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions. Lerche H; Biervert C; Alekov AK; Schleithoff L; Lindner M; Klinger W; Bretschneider F; Mitrovic N; Jurkat-Rott K; Bode H; Lehmann-Horn F; Steinlein OK Ann Neurol; 1999 Sep; 46(3):305-12. PubMed ID: 10482260 [TBL] [Abstract][Full Text] [Related]
28. Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy. Yang WP; Levesque PC; Little WA; Conder ML; Ramakrishnan P; Neubauer MG; Blanar MA J Biol Chem; 1998 Jul; 273(31):19419-23. PubMed ID: 9677360 [TBL] [Abstract][Full Text] [Related]
29. Subthreshold changes of voltage-dependent activation of the K(V)7.2 channel in neonatal epilepsy. Hunter J; Maljevic S; Shankar A; Siegel A; Weissman B; Holt P; Olson L; Lerche H; Escayg A Neurobiol Dis; 2006 Oct; 24(1):194-201. PubMed ID: 16916607 [TBL] [Abstract][Full Text] [Related]
30. Benign familial neonatal convulsions: novel mutation in a newborn. Lee IC; Chen JY; Chen YJ; Yu JS; Su PH Pediatr Neurol; 2009 May; 40(5):387-91. PubMed ID: 19380078 [TBL] [Abstract][Full Text] [Related]
31. The new voltage gated potassium channel KCNQ5 and neonatal convulsions. Kananura C; Biervert C; Hechenberger M; Engels H; Steinlein OK Neuroreport; 2000 Jun; 11(9):2063-7. PubMed ID: 10884071 [TBL] [Abstract][Full Text] [Related]
34. A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation. Borgatti R; Zucca C; Cavallini A; Ferrario M; Panzeri C; Castaldo P; Soldovieri MV; Baschirotto C; Bresolin N; Dalla Bernardina B; Taglialatela M; Bassi MT Neurology; 2004 Jul; 63(1):57-65. PubMed ID: 15249611 [TBL] [Abstract][Full Text] [Related]
35. [Molecular defects may cause epilepsy. New discoveries can provide better possibilities for directional diagnostics and treatment]. Brismar T Lakartidningen; 2000 Nov; 97(45):5102-6. PubMed ID: 11116887 [TBL] [Abstract][Full Text] [Related]
36. Lack of potassium current in W309R mutant KCNQ3 channel causing benign familial neonatal convulsions (BFNC). Sugiura Y; Nakatsu F; Hiroyasu K; Ishii A; Hirose S; Okada M; Jibiki I; Ohno H; Kaneko S; Ugawa Y Epilepsy Res; 2009 Mar; 84(1):82-5. PubMed ID: 19167866 [TBL] [Abstract][Full Text] [Related]
37. Deletions involving both KCNQ2 and CHRNA4 present with benign familial neonatal seizures. Kurahashi H; Wang JW; Ishii A; Kojima T; Wakai S; Kizawa T; Fujimoto Y; Kikkawa K; Yoshimura K; Inoue T; Yasumoto S; Ogawa A; Kaneko S; Hirose S Neurology; 2009 Oct; 73(15):1214-7. PubMed ID: 19822871 [TBL] [Abstract][Full Text] [Related]
38. Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel. Dedek K; Kunath B; Kananura C; Reuner U; Jentsch TJ; Steinlein OK Proc Natl Acad Sci U S A; 2001 Oct; 98(21):12272-7. PubMed ID: 11572947 [TBL] [Abstract][Full Text] [Related]
40. Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy. Cooper EC; Aldape KD; Abosch A; Barbaro NM; Berger MS; Peacock WS; Jan YN; Jan LY Proc Natl Acad Sci U S A; 2000 Apr; 97(9):4914-9. PubMed ID: 10781098 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]