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Journal Abstract Search

210 related items for PubMed ID: 15464434

  • 1. 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; 83(1-2):188-96. PubMed ID: 15464434
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  • 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; 25(3):295-300. PubMed ID: 16789403
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  • 5. 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; 94(11):1478-84. PubMed ID: 18467357
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  • 8. Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression.
    Keren A, Syrris P, McKenna WJ.
    Nat Clin Pract Cardiovasc Med; 2008 Mar; 5(3):158-68. PubMed ID: 18227814
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  • 9. [A novel missense mutation, K124N, in the troponin T gene of Chinese populations with hypertrophic cardiomyopathy].
    An FS, Zhang Y, Li DQ, Yang XS, Li L, Zhang C, Yan ML, Wang Y, An GP.
    Zhonghua Yi Xue Za Zhi; 2004 Aug 17; 84(16):1340-3. PubMed ID: 15387941
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  • 11. Molecular genetics of familial hypertrophic cardiomyopathy (FHC).
    Bashyam MD, Savithri GR, Kumar MS, Narasimhan C, Nallari P.
    J Hum Genet; 2003 Aug 17; 48(2):55-64. PubMed ID: 12601548
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  • 16. Familial and sporadic hypertrophic myopathy: differences and similarities in a genotyped population. A long follow-up study.
    Brito D, Richard P, Komajda M, Madeira H.
    Rev Port Cardiol; 2008 Feb 17; 27(2):147-73. PubMed ID: 18488914
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  • 18. Phenotypic differences between electrocardiographic and echocardiographic determination of hypertrophic cardiomyopathy in genetically affected subjects.
    Konno T, Shimizu M, Ino H, Fujino N, Hayashi K, Uchiyama K, Kaneda T, Inoue M, Masuda E, Mabuchi H.
    J Intern Med; 2005 Sep 17; 258(3):216-24. PubMed ID: 16115294
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  • 19. A familial hypertrophic cardiomyopathy alpha-tropomyosin mutation causes severe cardiac hypertrophy and death in mice.
    Prabhakar R, Boivin GP, Grupp IL, Hoit B, Arteaga G, Solaro RJ, Wieczorek DF.
    J Mol Cell Cardiol; 2001 Oct 17; 33(10):1815-28. PubMed ID: 11603924
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