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

386 related items for PubMed ID: 15542288

  • 1. Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy.
    Mogensen J, Murphy RT, Shaw T, Bahl A, Redwood C, Watkins H, Burke M, Elliott PM, McKenna WJ.
    J Am Coll Cardiol; 2004 Nov 16; 44(10):2033-40. PubMed ID: 15542288
    [Abstract] [Full Text] [Related]

  • 2. Familial dilated cardiomyopathy with troponin T K210del mutation.
    Martins E, Silva-Cardoso J, Alves C, Pereira H, Soares B, Damasceno A, Abreu-Lima C, Amorim A, Rocha-Gonçalves F.
    Rev Port Cardiol; 2006 Mar 16; 25(3):295-300. PubMed ID: 16789403
    [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. Exome Sequencing Identifies Pathogenic and Modifier Mutations in a Child With Sporadic Dilated Cardiomyopathy.
    Long PA, Larsen BT, Evans JM, Olson TM.
    J Am Heart Assoc; 2015 Dec 09; 4(12):. PubMed ID: 26656454
    [Abstract] [Full Text] [Related]

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

  • 8. Genotype-specific pathogenic effects in human dilated cardiomyopathy.
    Bollen IAE, Schuldt M, Harakalova M, Vink A, Asselbergs FW, Pinto JR, Krüger M, Kuster DWD, van der Velden J.
    J Physiol; 2017 Jul 15; 595(14):4677-4693. PubMed ID: 28436080
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 11. Two novel mutations in the beta-myosin heavy chain gene associated with dilated cardiomyopathy.
    Kärkkäinen S, Heliö T, Jääskeläinen P, Miettinen R, Tuomainen P, Ylitalo K, Kaartinen M, Reissell E, Toivonen L, Nieminen MS, Kuusisto J, Laakso M, Peuhkurinen K.
    Eur J Heart Fail; 2004 Dec 15; 6(7):861-8. PubMed ID: 15556047
    [Abstract] [Full Text] [Related]

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

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

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy.
    Kamisago M, Sharma SD, DePalma SR, Solomon S, Sharma P, McDonough B, Smoot L, Mullen MP, Woolf PK, Wigle ED, Seidman JG, Seidman CE.
    N Engl J Med; 2000 Dec 07; 343(23):1688-96. PubMed ID: 11106718
    [Abstract] [Full Text] [Related]

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

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

  • 18. Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy.
    Mogensen J, Murphy RT, Kubo T, Bahl A, Moon JC, Klausen IC, Elliott PM, McKenna WJ.
    J Am Coll Cardiol; 2004 Dec 21; 44(12):2315-25. PubMed ID: 15607392
    [Abstract] [Full Text] [Related]

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

  • 20. Novel troponin T mutation in familial dilated cardiomyopathy with gender-dependant severity.
    Stefanelli CB, Rosenthal A, Borisov AB, Ensing GJ, Russell MW.
    Mol Genet Metab; 2004 Dec 21; 83(1-2):188-96. PubMed ID: 15464434
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 20.