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382 related items for PubMed ID: 16789403

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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 Mar; 83(1-2):188-96. PubMed ID: 15464434
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  • 3. Portuguese study of familial dilated cardiomyopathy: the FATIMA study.
    Martins E, Silva-Cardoso J, Bicho M, Bourbon M, Ceia F, Rebocho MJ, Moura B, Fonseca C, Correia MJ, Brito D, Perdigão C, Madeira H, Abreu-Lima C.
    Rev Port Cardiol; 2008 Sep; 27(9):1029-42. PubMed ID: 19044174
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  • 4. Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences.
    Doolan A, Tebo M, Ingles J, Nguyen L, Tsoutsman T, Lam L, Chiu C, Chung J, Weintraub RG, Semsarian C.
    J Mol Cell Cardiol; 2005 Feb; 38(2):387-93. PubMed ID: 15698845
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  • 5. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics.
    van Tintelen JP, Hofstra RM, Katerberg H, Rossenbacker T, Wiesfeld AC, du Marchie Sarvaas GJ, Wilde AA, van Langen IM, Nannenberg EA, van der Kooi AJ, Kraak M, van Gelder IC, van Veldhuisen DJ, Vos Y, van den Berg MP, Working Group on Inherited Cardiac Disorders, line 27/50, Interuniversity Cardiology Institute of The Netherlands.
    Am Heart J; 2007 Dec; 154(6):1130-9. PubMed ID: 18035086
    [Abstract] [Full Text] [Related]

  • 6. Familial dilated cardiomyopathy: evidence for clinical and immunogenetic heterogeneity.
    Bilińska ZT, Michalak E, Piatosa B, Grzybowski J, Skwarek M, Deptuch TW, Kuśmierczyk-Droszcz B, Piotrowski W, Ruzyłło W.
    Med Sci Monit; 2003 May; 9(5):CR167-74. PubMed ID: 12761452
    [Abstract] [Full Text] [Related]

  • 7. [Family hypertrophic cardiomyopathy caused by a 14035c > t mutation in cardiac troponin T gene].
    Wang SX, Zou YB, Fu CY, Song L, Wang H, Wang JZ, Song XD, Chen JZ, Hui RT.
    Zhonghua Yi Xue Za Zhi; 2007 Feb 06; 87(6):371-4. PubMed ID: 17456375
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 16; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 10. 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 16; 94(11):1478-84. PubMed ID: 18467357
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  • 12. [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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  • 14. Epidemiology of desmin and cardiac actin gene mutations in a european population of dilated cardiomyopathy.
    Tesson F, Sylvius N, Pilotto A, Dubosq-Bidot L, Peuchmaurd M, Bouchier C, Benaiche A, Mangin L, Charron P, Gavazzi A, Tavazzi L, Arbustini E, Komajda M.
    Eur Heart J; 2000 Nov 17; 21(22):1872-6. PubMed ID: 11052860
    [Abstract] [Full Text] [Related]

  • 15. Severe familial left ventricular non-compaction cardiomyopathy due to a novel troponin T (TNNT2) mutation.
    Luedde M, Ehlermann P, Weichenhan D, Will R, Zeller R, Rupp S, Müller A, Steen H, Ivandic BT, Ulmer HE, Kern M, Katus HA, Frey N.
    Cardiovasc Res; 2010 Jun 01; 86(3):452-60. PubMed ID: 20083571
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  • 17. Molecular evaluation of five cardiac genes in Doberman Pinschers with dilated cardiomyopathy.
    Meurs KM, Hendrix KP, Norgard MM.
    Am J Vet Res; 2008 Aug 01; 69(8):1050-3. PubMed ID: 18672969
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  • 20. Familial dilated cardiomyopathy secondary to dystrophin splice site mutation.
    Obler D, Wu BL, Lip V, Estrella E, Keck S, Haggan C, Semigran M, Smoot LB.
    J Card Fail; 2010 Mar 01; 16(3):194-9. PubMed ID: 20206892
    [Abstract] [Full Text] [Related]

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