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

203 related items for PubMed ID: 11844290

  • 1. Variable expression of long QT syndrome among gene carriers from families with five different HERG mutations.
    Benhorin J, Moss AJ, Bak M, Zareba W, Kaufman ES, Kerem B, Towbin JA, Priori S, Kass RS, Attali B, Brown AM, Ficker E.
    Ann Noninvasive Electrocardiol; 2002 Jan; 7(1):40-6. PubMed ID: 11844290
    [Abstract] [Full Text] [Related]

  • 2. Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.
    Zareba W, Moss AJ, Locati EH, Lehmann MH, Peterson DR, Hall WJ, Schwartz PJ, Vincent GM, Priori SG, Benhorin J, Towbin JA, Robinson JL, Andrews ML, Napolitano C, Timothy K, Zhang L, Medina A, International Long QT Syndrome Registry.
    J Am Coll Cardiol; 2003 Jul 02; 42(1):103-9. PubMed ID: 12849668
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No 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. Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.
    Swan H, Viitasalo M, Piippo K, Laitinen P, Kontula K, Toivonen L.
    J Am Coll Cardiol; 1999 Sep 02; 34(3):823-9. PubMed ID: 10483966
    [Abstract] [Full Text] [Related]

  • 9. Q-T peak dispersion in congenital long QT syndrome: possible marker of mutation of HERG.
    Inoue M, Shimizu M, Ino H, Yamaguchi M, Terai H, Hayashi K, Kiyama M, Sakata K, Hayashi T, Mabuchi H.
    Circ J; 2003 Jun 02; 67(6):495-8. PubMed ID: 12808265
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 12. The inherited long QT syndrome: from ion channel to bedside.
    Vincent GM, Timothy K, Fox J, Zhang L.
    Cardiol Rev; 1999 Jun 02; 7(1):44-55. PubMed ID: 10348966
    [Abstract] [Full Text] [Related]

  • 13. Identical twins with long QT syndrome associated with a missense mutation in the S4 region of the HERG.
    Hayashi K, Shimizu M, Ino H, Okeie K, Yamaguchi M, Yasuda T, Fujino N, Fujii H, Fujita S, Mabuchi H.
    Jpn Heart J; 2000 May 02; 41(3):399-404. PubMed ID: 10987356
    [Abstract] [Full Text] [Related]

  • 14. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
    Vincent GM.
    Annu Rev Med; 1998 May 02; 49():263-74. PubMed ID: 9509262
    [Abstract] [Full Text] [Related]

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

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.