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Journal Abstract Search

670 related items for PubMed ID: 20298698

  • 1. Malignant and benign mutations in familial cardiomyopathies: insights into mutations linked to complex cardiovascular phenotypes.
    Xu Q, Dewey S, Nguyen S, Gomes AV.
    J Mol Cell Cardiol; 2010 May; 48(5):899-909. PubMed ID: 20298698
    [Abstract] [Full Text] [Related]

  • 2. [Hereditary cardiomyopathies: a review. Mutation of structural proteins a common cause of hereditary cardiomyopathy].
    Sjöberg G, Kostareva A, Sejersen T.
    Lakartidningen; 2010 May; 102(11):845-7, 850-3. PubMed ID: 15835520
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  • 3. Mutations in Troponin that cause HCM, DCM AND RCM: what can we learn about thin filament function?
    Willott RH, Gomes AV, Chang AN, Parvatiyar MS, Pinto JR, Potter JD.
    J Mol Cell Cardiol; 2010 May; 48(5):882-92. PubMed ID: 19914256
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  • 4. Novel locus for an inherited cardiomyopathy maps to chromosome 7.
    Song L, DePalma SR, Kharlap M, Zenovich AG, Cirino A, Mitchell R, McDonough B, Maron BJ, Seidman CE, Seidman JG, Ho CY.
    Circulation; 2006 May 09; 113(18):2186-92. PubMed ID: 16651466
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  • 5. Molecular and cellular aspects of troponin cardiomyopathies.
    Gomes AV, Potter JD.
    Ann N Y Acad Sci; 2004 May 09; 1015():214-24. PubMed ID: 15201162
    [Abstract] [Full Text] [Related]

  • 6. Molecular mechanisms of inherited cardiomyopathies.
    Fatkin D, Graham RM.
    Physiol Rev; 2002 Oct 09; 82(4):945-80. PubMed ID: 12270949
    [Abstract] [Full Text] [Related]

  • 7. [Mutations in genes for sarcomeric proteins].
    Kimura A.
    Nihon Rinsho; 2000 Jan 09; 58(1):117-22. PubMed ID: 10885298
    [Abstract] [Full Text] [Related]

  • 8. Alpha-myosin heavy chain: a sarcomeric gene associated with dilated and hypertrophic phenotypes of cardiomyopathy.
    Carniel E, Taylor MR, Sinagra G, Di Lenarda A, Ku L, Fain PR, Boucek MM, Cavanaugh J, Miocic S, Slavov D, Graw SL, Feiger J, Zhu XZ, Dao D, Ferguson DA, Bristow MR, Mestroni L.
    Circulation; 2005 Jul 05; 112(1):54-9. PubMed ID: 15998695
    [Abstract] [Full Text] [Related]

  • 9. 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 05; 94(11):1478-84. PubMed ID: 18467357
    [Abstract] [Full Text] [Related]

  • 10. Inflammatory dilated cardiomyopathy (DCMI).
    Maisch B, Richter A, Sandmöller A, Portig I, Pankuweit S, BMBF-Heart Failure Network.
    Herz; 2005 Sep 05; 30(6):535-44. PubMed ID: 16170686
    [Abstract] [Full Text] [Related]

  • 11. Hypertrophic cardiomyopathy: from gene defect to clinical disease.
    Chung MW, Tsoutsman T, Semsarian C.
    Cell Res; 2003 Feb 05; 13(1):9-20. PubMed ID: 12643345
    [Abstract] [Full Text] [Related]

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  • 13. Prevalence, clinical significance, and genetic basis of hypertrophic cardiomyopathy with restrictive phenotype.
    Kubo T, Gimeno JR, Bahl A, Steffensen U, Steffensen M, Osman E, Thaman R, Mogensen J, Elliott PM, Doi Y, McKenna WJ.
    J Am Coll Cardiol; 2007 Jun 26; 49(25):2419-26. PubMed ID: 17599605
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  • 17. Sarcomeric proteins and inherited cardiomyopathies.
    Morimoto S.
    Cardiovasc Res; 2008 Mar 01; 77(4):659-66. PubMed ID: 18056765
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  • 18. Furthering the link between the sarcomere and primary cardiomyopathies: restrictive cardiomyopathy associated with multiple mutations in genes previously associated with hypertrophic or dilated cardiomyopathy.
    Caleshu C, Sakhuja R, Nussbaum RL, Schiller NB, Ursell PC, Eng C, De Marco T, McGlothlin D, Burchard EG, Rame JE.
    Am J Med Genet A; 2011 Sep 01; 155A(9):2229-35. PubMed ID: 21823217
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