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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

151 related items for PubMed ID: 16883520

  • 1. [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
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. 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, BFNC Physician Consortium.
    Brain; 2003 Dec; 126(Pt 12):2726-37. PubMed ID: 14534157
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. 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
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. A novel mutation of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions.
    Li H, Li N, Shen L, Jiang H, Yang Q, Song Y, Guo J, Xia K, Pan Q, Tang B.
    Epilepsy Res; 2008 Mar; 79(1):1-5. PubMed ID: 18249525
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes.
    Neubauer BA, Waldegger S, Heinzinger J, Hahn A, Kurlemann G, Fiedler B, Eberhard F, Muhle H, Stephani U, Garkisch S, Eeg-Olofsson O, Müller U, Sander T.
    Neurology; 2008 Jul 15; 71(3):177-83. PubMed ID: 18625963
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.
    Charlier C, Singh NA, Ryan SG, Lewis TB, Reus BE, Leach RJ, Leppert M.
    Nat Genet; 1998 Jan 15; 18(1):53-5. PubMed ID: 9425900
    [Abstract] [Full Text] [Related]

  • 17. Benign familial neonatal convulsions: novel mutation in a newborn.
    Lee IC, Chen JY, Chen YJ, Yu JS, Su PH.
    Pediatr Neurol; 2009 May 15; 40(5):387-91. PubMed ID: 19380078
    [Abstract] [Full Text] [Related]

  • 18. Novel mutation in KCNQ2 causing benign familial neonatal seizures.
    Goldberg-Stern H, Kaufmann R, Kivity S, Afawi Z, Heron SE.
    Pediatr Neurol; 2009 Nov 15; 41(5):367-70. PubMed ID: 19818940
    [Abstract] [Full Text] [Related]

  • 19. [A novel mutation in KCNQ2 gene causes benign familial infantile convulsions (BFIC) in a Chinese family].
    Zhou XH, Ma AQ, Liu XH, Huang C, Zhang YM, Shi RM.
    Zhonghua Er Ke Za Zhi; 2006 Jul 15; 44(7):487-91. PubMed ID: 17044971
    [Abstract] [Full Text] [Related]

  • 20. Benign familial neonatal convulsions (BFNC) resulting from mutation of the KCNQ2 voltage sensor.
    Miraglia del Giudice E, Coppola G, Scuccimarra G, Cirillo G, Bellini G, Pascotto A.
    Eur J Hum Genet; 2000 Dec 15; 8(12):994-7. PubMed ID: 11175290
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.