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

311 related items for PubMed ID: 12566525

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
    Vincent GM.
    Annu Rev Med; 1998; 49():263-74. PubMed ID: 9509262
    [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. [Genetic background predisposing the drug-induced long QT syndrome].
    Horie M.
    Nihon Yakurigaku Zasshi; 2003 Jun; 121(6):401-7. PubMed ID: 12835534
    [Abstract] [Full Text] [Related]

  • 10. KCNQ1 and KCNH2 mutations associated with long QT syndrome in a Chinese population.
    Liu W, Yang J, Hu D, Kang C, Li C, Zhang S, Li P, Chen Z, Qin X, Ying K, Li Y, Li Y, Li Z, Cheng X, Li L, Qi Y, Chen S, Wang Q.
    Hum Mutat; 2002 Dec; 20(6):475-6. PubMed ID: 12442276
    [Abstract] [Full Text] [Related]

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

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 14. 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]

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

  • 16. Molecular biology and cellular mechanisms of Brugada and long QT syndromes in infants and young children.
    Antzelevitch C.
    J Electrocardiol; 2001 Jul 02; 34 Suppl():177-81. PubMed ID: 11781953
    [Abstract] [Full Text] [Related]

  • 17. Long QT syndrome: more questions.
    Moss AJ.
    J Cardiovasc Electrophysiol; 2001 Apr 02; 12(4):462. PubMed ID: 11332569
    [No Abstract] [Full Text] [Related]

  • 18. [Etiological mechanism of long QT syndrome and the effects of macrolides].
    Kato T.
    Jpn J Antibiot; 2001 Feb 02; 54 Suppl A():118-22. PubMed ID: 11439888
    [No Abstract] [Full Text] [Related]

  • 19. Novel missense mutation (G601S) of HERG in a Japanese long QT syndrome family.
    Akimoto K, Furutani M, Imamura S, Furutani Y, Kasanuki H, Takao A, Momma K, Matsuoka R.
    Hum Mutat; 1998 Feb 02; Suppl 1():S184-6. PubMed ID: 9452080
    [No Abstract] [Full Text] [Related]

  • 20. A plethora of mechanisms in the HERG-related long QT syndrome. Genetics meets electrophysiology.
    Roden DM, Balser JR.
    Cardiovasc Res; 1999 Nov 02; 44(2):242-6. PubMed ID: 10690299
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 16.