155 related articles for article (PubMed ID: 16883520)
21. A novel mutation of KCNQ3 (c.925T-->C) in a Japanese family with benign familial neonatal convulsions.
Hirose S; Zenri F; Akiyoshi H; Fukuma G; Iwata H; Inoue T; Yonetani M; Tsutsumi M; Muranaka H; Kurokawa T; Hanai T; Wada K; Kaneko S; Mitsudome A
Ann Neurol; 2000 Jun; 47(6):822-6. PubMed ID: 10852552
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions.
Ishii A; Fukuma G; Uehara A; Miyajima T; Makita Y; Hamachi A; Yasukochi M; Inoue T; Yasumoto S; Okada M; Kaneko S; Mitsudome A; Hirose S
Brain Dev; 2009 Jan; 31(1):27-33. PubMed ID: 18640800
[TBL] [Abstract][Full Text] [Related]
25. Developmental changes in KCNQ2 and KCNQ3 expression in human brain: possible contribution to the age-dependent etiology of benign familial neonatal convulsions.
Kanaumi T; Takashima S; Iwasaki H; Itoh M; Mitsudome A; Hirose S
Brain Dev; 2008 May; 30(5):362-9. PubMed ID: 18166285
[TBL] [Abstract][Full Text] [Related]
26. Role of KCNQ2 and KCNQ3 genes in juvenile idiopathic epilepsy in Arabian foals.
Lichter-Peled A; Polani S; Stanyon R; Rocchi M; Kahila Bar-Gal G
Vet J; 2013 Apr; 196(1):57-63. PubMed ID: 23182620
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Benign neonatal sleep myoclonus: an autosomal dominant form not allelic to KCNQ2 or KCNQ3.
Afawi Z; Bassan H; Heron S; Oliver K; Straussberg R; Scheffer I; Leventer R; Korczyn A; Berkovic S
J Child Neurol; 2012 Oct; 27(10):1260-3. PubMed ID: 22447848
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. De novo KCNQ2 mutations in patients with benign neonatal seizures.
Claes LR; Ceulemans B; Audenaert D; Deprez L; Jansen A; Hasaerts D; Weckx S; Claeys KG; Del-Favero J; Van Broeckhoven C; De Jonghe P
Neurology; 2004 Dec; 63(11):2155-8. PubMed ID: 15596769
[TBL] [Abstract][Full Text] [Related]
31. Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3.
Heron SE; Scheffer IE; Grinton BE; Eyre H; Oliver KL; Bain S; Berkovic SF; Mulley JC
Epilepsia; 2010 Sep; 51(9):1865-9. PubMed ID: 20384724
[TBL] [Abstract][Full Text] [Related]
32. Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures.
Heron SE; Cox K; Grinton BE; Zuberi SM; Kivity S; Afawi Z; Straussberg R; Berkovic SF; Scheffer IE; Mulley JC
J Med Genet; 2007 Dec; 44(12):791-6. PubMed ID: 17675531
[TBL] [Abstract][Full Text] [Related]
33. Benign familial neonatal convulsions: always benign?
Steinlein OK; Conrad C; Weidner B
Epilepsy Res; 2007 Mar; 73(3):245-9. PubMed ID: 17129708
[TBL] [Abstract][Full Text] [Related]
34. A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts.
Ma X; Li FF; Wang SZ; Gao C; Zhang M; Zhu SQ
Mol Vis; 2008; 14():1906-11. PubMed ID: 18958306
[TBL] [Abstract][Full Text] [Related]
35. Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization.
Singh NA; Otto JF; Dahle EJ; Pappas C; Leslie JD; Vilaythong A; Noebels JL; White HS; Wilcox KS; Leppert MF
J Physiol; 2008 Jul; 586(14):3405-23. PubMed ID: 18483067
[TBL] [Abstract][Full Text] [Related]
36. Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions.
Vanmolkot KR; Kors EE; Hottenga JJ; Terwindt GM; Haan J; Hoefnagels WA; Black DF; Sandkuijl LA; Frants RR; Ferrari MD; van den Maagdenberg AM
Ann Neurol; 2003 Sep; 54(3):360-6. PubMed ID: 12953268
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Benign infantile familial convulsions are not an allelic form of the benign familial neonatal convulsions gene.
Malafosse A; Beck C; Bellet H; Di Capua M; Dulac O; Echenne B; Fusco L; Lucchini P; Ricci S; Sebastianelli R
Ann Neurol; 1994 Apr; 35(4):479-82. PubMed ID: 8154876
[TBL] [Abstract][Full Text] [Related]
39. A nonsense mutation in the alpha4 subunit of the nicotinic acetylcholine receptor (CHRNA4) cosegregates with 20q-linked benign neonatal familial convulsions (EBNI).
Beck C; Moulard B; Steinlein O; Guipponi M; Vallee L; Montpied P; Baldy-Moulnier M; Malafosse A
Neurobiol Dis; 1994 Nov; 1(1-2):95-9. PubMed ID: 9216991
[TBL] [Abstract][Full Text] [Related]
40. The first Korean case of KCNQ2 mutation in a family with benign familial neonatal convulsions.
Yum MS; Ko TS; Yoo HW
J Korean Med Sci; 2010 Feb; 25(2):324-6. PubMed ID: 20119593
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
