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

284 related items for PubMed ID: 12601548

  • 1. Molecular genetics of familial hypertrophic cardiomyopathy (FHC).
    Bashyam MD, Savithri GR, Kumar MS, Narasimhan C, Nallari P.
    J Hum Genet; 2003; 48(2):55-64. PubMed ID: 12601548
    [Abstract] [Full Text] [Related]

  • 2. [Familial hypertrophic cardiomyopathy: genes, mutations and animal models. A review].
    Ramírez CD, Padrón R.
    Invest Clin; 2004 Mar; 45(1):69-99. PubMed ID: 15058760
    [Abstract] [Full Text] [Related]

  • 3. Microvascular function is selectively impaired in patients with hypertrophic cardiomyopathy and sarcomere myofilament gene mutations.
    Olivotto I, Girolami F, Sciagrà R, Ackerman MJ, Sotgia B, Bos JM, Nistri S, Sgalambro A, Grifoni C, Torricelli F, Camici PG, Cecchi F.
    J Am Coll Cardiol; 2011 Aug 16; 58(8):839-48. PubMed ID: 21835320
    [Abstract] [Full Text] [Related]

  • 4. Mutations in sarcomere protein genes in left ventricular noncompaction.
    Klaassen S, Probst S, Oechslin E, Gerull B, Krings G, Schuler P, Greutmann M, Hürlimann D, Yegitbasi M, Pons L, Gramlich M, Drenckhahn JD, Heuser A, Berger F, Jenni R, Thierfelder L.
    Circulation; 2008 Jun 03; 117(22):2893-901. PubMed ID: 18506004
    [Abstract] [Full Text] [Related]

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

  • 6. Familial hypertrophic cardiomiopathy: molecular basis and genotype-phenotype correlations.
    Cuda G, Lamberti A, Perrotti N, Perticone F, Mattioli PL.
    Rev Port Cardiol; 1998 Oct 03; 17 Suppl 2():II21-31. PubMed ID: 9835779
    [Abstract] [Full Text] [Related]

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

  • 8. The molecular genetics of hypertrophic cardiomyopathy: prognostic implications.
    Sorajja P, Elliott PM, McKenna WJ.
    Europace; 2000 Jan 03; 2(1):4-14. PubMed ID: 11225594
    [No Abstract] [Full Text] [Related]

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

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

  • 11. Genetic diagnosis of hypertrophic cardiomyopathy using mass spectrometry DNA arrays and high resolution melting.
    Santos S, Lança V, Oliveira H, Branco P, Silveira L, Marques V, Brito D, Madeira H, Bicho M, Fernandes AR.
    Rev Port Cardiol; 2011 Jan 03; 30(1):7-18. PubMed ID: 21425739
    [Abstract] [Full Text] [Related]

  • 12. Sarcomeric proteins and familial hypertrophic cardiomyopathy: linking mutations in structural proteins to complex cardiovascular phenotypes.
    Tardiff JC.
    Heart Fail Rev; 2005 Sep 03; 10(3):237-48. PubMed ID: 16416046
    [Abstract] [Full Text] [Related]

  • 13. Genetics of hypertrophic cardiomyopathy after 20 years: clinical perspectives.
    Maron BJ, Maron MS, Semsarian C.
    J Am Coll Cardiol; 2012 Aug 21; 60(8):705-15. PubMed ID: 22796258
    [Abstract] [Full Text] [Related]

  • 14. A contemporary approach to hypertrophic cardiomyopathy.
    Ho CY, Seidman CE.
    Circulation; 2006 Jun 20; 113(24):e858-62. PubMed ID: 16785342
    [No Abstract] [Full Text] [Related]

  • 15. [Mutations in genes for sarcomeric proteins].
    Kimura A.
    Nihon Rinsho; 2000 Jan 20; 58(1):117-22. PubMed ID: 10885298
    [Abstract] [Full Text] [Related]

  • 16. Familial hypertrophic cardiomyopathy: a paradigm of the cardiac hypertrophic response to injury.
    Marian AJ, Roberts R.
    Ann Med; 1998 Aug 20; 30 Suppl 1():24-32. PubMed ID: 9800880
    [Abstract] [Full Text] [Related]

  • 17. A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy.
    Semsarian C, Healey MJ, Fatkin D, Giewat M, Duffy C, Seidman CE, Seidman JG.
    J Mol Cell Cardiol; 2001 Nov 20; 33(11):2055-60. PubMed ID: 11708849
    [Abstract] [Full Text] [Related]

  • 18. Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes.
    Kaski JP, Syrris P, Burch M, Tomé-Esteban MT, Fenton M, Christiansen M, Andersen PS, Sebire N, Ashworth M, Deanfield JE, McKenna WJ, Elliott PM.
    Heart; 2008 Nov 20; 94(11):1478-84. PubMed ID: 18467357
    [Abstract] [Full Text] [Related]

  • 19. Familial hypertrophic cardiomyopathy: functional effects of myosin mutation R723G in cardiomyocytes.
    Kraft T, Witjas-Paalberends ER, Boontje NM, Tripathi S, Brandis A, Montag J, Hodgkinson JL, Francino A, Navarro-Lopez F, Brenner B, Stienen GJ, van der Velden J.
    J Mol Cell Cardiol; 2013 Apr 20; 57():13-22. PubMed ID: 23318932
    [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 Apr 20; 83(1-2):188-96. PubMed ID: 15464434
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.