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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 10961643)

  • 41. Cloning and mutation analysis of the human potassium channel KCNQ2 gene promoter.
    Xiao JF; Fischer C; Steinlein OK
    Neuroreport; 2001 Dec; 12(17):3733-9. PubMed ID: 11726784
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Potassium channels: how genetic studies of epileptic syndromes open paths to new therapeutic targets and drugs.
    Cooper EC
    Epilepsia; 2001; 42 Suppl 5():49-54. PubMed ID: 11887968
    [TBL] [Abstract][Full Text] [Related]  

  • 43. 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]  

  • 44. 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]  

  • 45. 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]  

  • 46. Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation.
    Blumkin L; Suls A; Deconinck T; De Jonghe P; Linder I; Kivity S; Dabby R; Leshinsky-Silver E; Lev D; Lerman-Sagie T
    Eur J Paediatr Neurol; 2012 Jul; 16(4):356-60. PubMed ID: 22169383
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Neuronal KCNQ potassium channels: physiology and role in disease.
    Jentsch TJ
    Nat Rev Neurosci; 2000 Oct; 1(1):21-30. PubMed ID: 11252765
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Benign familial neonatal convulsions: confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8q.
    Steinlein O; Schuster V; Fischer C; Häussler M
    Hum Genet; 1995 Apr; 95(4):411-5. PubMed ID: 7705837
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [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]  

  • 50. 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]  

  • 51. [Clinical and mutational analysis of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions].
    Li HY; Tang BS; Yan XX; Guo JF; Shen L; Song YM; Jiang H; Xia K; Xie ZG; Yang QA
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Aug; 23(4):374-7. PubMed ID: 16883520
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Potassium channel genes and benign familial neonatal epilepsy.
    Maljevic S; Lerche H
    Prog Brain Res; 2014; 213():17-53. PubMed ID: 25194482
    [TBL] [Abstract][Full Text] [Related]  

  • 53. New human sodium/glucose cotransporter gene (KST1): identification, characterization, and mutation analysis in ICCA (infantile convulsions and choreoathetosis) and BFIC (benign familial infantile convulsions) families.
    Roll P; Massacrier A; Pereira S; Robaglia-Schlupp A; Cau P; Szepetowski P
    Gene; 2002 Feb; 285(1-2):141-8. PubMed ID: 12039040
    [TBL] [Abstract][Full Text] [Related]  

  • 54. 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]  

  • 55. Phenotypes of children with 20q13.3 microdeletion affecting KCNQ2 and CHRNA4.
    Okumura A; Atsushi Ishii ; Shimojima K; Kurahashi H; Yoshitomi S; lmai K; Imamura M; Seki Y; Toshiaki Shimizu T; Hirose S; Yamamoto T
    Epileptic Disord; 2015 Jun; 17(2):165-71. PubMed ID: 26030193
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance.
    Zara F; Specchio N; Striano P; Robbiano A; Gennaro E; Paravidino R; Vanni N; Beccaria F; Capovilla G; Bianchi A; Caffi L; Cardilli V; Darra F; Bernardina BD; Fusco L; Gaggero R; Giordano L; Guerrini R; Incorpora G; Mastrangelo M; Spaccini L; Laverda AM; Vecchi M; Vanadia F; Veggiotti P; Viri M; Occhi G; Budetta M; Taglialatela M; Coviello DA; Vigevano F; Minetti C
    Epilepsia; 2013 Mar; 54(3):425-36. PubMed ID: 23360469
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome.
    Terwindt GM; Ophoff RA; Lindhout D; Haan J; Halley DJ; Sandkuijl LA; Brouwer OF; Frants RR; Ferrari MD
    Epilepsia; 1997 Aug; 38(8):915-21. PubMed ID: 9579893
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Neonatal epilepsy syndromes and GEFS+: mechanistic considerations.
    Burgess DL
    Epilepsia; 2005; 46 Suppl 10():51-8. PubMed ID: 16359473
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Andreas Rett and benign familial neonatal convulsions revisited.
    Zimprich F; Ronen GM; Stögmann W; Baumgartner C; Stögmann E; Rett B; Pappas C; Leppert M; Singh N; Anderson VE
    Neurology; 2006 Sep; 67(5):864-6. PubMed ID: 16966552
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Proposed genetic classification of the "benign" familial neonatal and infantile epilepsies.
    Mulley JC; Heron SE; Dibbens LM
    Epilepsia; 2011 Mar; 52(3):649-50. PubMed ID: 21395569
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.