Resultados da busca - Diane Fatkin

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  1. 1
    Genes and Atrial Fibrillation

    Genes and Atrial Fibrillation por Diane Fatkin, Robyn Otway, Jamie I. Vandenberg

    Publicado em 2007
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  2. 2
    Relations between left atrial appendage blood flow velocity, spontaneous echocardiographic contrast and thromboembolic risk in vivo

    Relations between left atrial appendage blood flow velocity, spontaneous echocardiographic contrast and thromboembolic risk in vivo por Diane Fatkin, Raymond P. Kelly, Michael P. Feneley

    Publicado em 1994
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  3. 3
    Genetics and Disease of Ventricular Muscle

    Genetics and Disease of Ventricular Muscle por Diane Fatkin, Christine E. Seidman, J G Seidman

    Publicado em 2014
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  4. 4
    Percutaneous balloon mitral valvotomy with the Inoue single-balloon catheter: Commissural morphology as a determinant of outcome

    Percutaneous balloon mitral valvotomy with the Inoue single-balloon catheter: Commissural morphology as a determinant of outcome por Diane Fatkin, P. Roy, John J. B. Morgan, Michael P. Feneley

    Publicado em 1993
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  5. 5
    Mutation of HAIRY-AND-ENHANCER-OF-SPLIT-7 in humans causes spondylocostal dysostosis

    Mutation of HAIRY-AND-ENHANCER-OF-SPLIT-7 in humans causes spondylocostal dysostosis por Duncan B. Sparrow, Encarna Guillén‐Navarro, Diane Fatkin, Sally L. Dunwoodie

    Publicado em 2008
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  6. 6
    Arrhythmic Genotypes in Familial Dilated Cardiomyopathy: Implications for Genetic Testing and Clinical Management

    Arrhythmic Genotypes in Familial Dilated Cardiomyopathy: Implications for Genetic Testing and Clinical Management por Stacey Peters, Saurabh Kumar, Perry Elliott, Jonathan M. Kalman, Diane Fatkin

    Publicado em 2018
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  7. 7
    Genetic testing in cardiovascular disease

    Genetic testing in cardiovascular disease por Michael P. Gray, Diane Fatkin, Jodie Ingles, E. Robertson, Gemma A. Figtree

    Publicado em 2024
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  8. 8
    Familial Dilated Cardiomyopathy

    Familial Dilated Cardiomyopathy por Stacey Peters, Renée Johnson, Samuel Birch, Dominica Zentner, Ray E. Hershberger, Diane Fatkin

    Publicado em 2019
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  9. 9
    Precision Medicine in the Management of Dilated Cardiomyopathy

    Precision Medicine in the Management of Dilated Cardiomyopathy por Diane Fatkin, Inken G. Huttner, Jason C. Kovacic, Jonathan G. Seidman, Christine E. Seidman

    Publicado em 2019
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  10. 10
    Decreased Bone Formation and Osteopenia in Lamin A/C-Deficient Mice

    Decreased Bone Formation and Osteopenia in Lamin A/C-Deficient Mice por Wei Li, Li Sze Yeo, Christopher Vidal, Thomas McCorquodale, Markus Herrmann, Diane Fatkin, Gustavo Duque

    Publicado em 2011
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  11. 11
    Analysis of protein sequence and interaction data for candidate disease gene prediction

    Analysis of protein sequence and interaction data for candidate disease gene prediction por Richard A. George, Jason Y. Liu, Lina Feng, Robert J. Bryson‐Richardson, Diane Fatkin, Merridee A. Wouters

    Publicado em 2006
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  12. 12
    Standardized echocardiographic assessment of cardiac function in normal adult zebrafish and heart disease models

    Standardized echocardiographic assessment of cardiac function in normal adult zebrafish and heart disease models por Louis W. Wang, Inken G. Huttner, Celine Santiago, Scott Kesteven, Ze Yu, Michael P. Feneley, Diane Fatkin

    Publicado em 2016
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  13. 13
    Arrhythmic Phenotypes Are a Defining Feature of Dilated Cardiomyopathy-Associated <i>SCN5A</i> Variants: A Systematic Review

    Arrhythmic Phenotypes Are a Defining Feature of Dilated Cardiomyopathy-Associated <i>SCN5A</i> Variants: A Systematic Review por Stacey Peters, Bryony A. Thompson, Mark J. Perrin, Paul A. James, Dominica Zentner, Jonathan M. Kalman, Jamie I. Vandenberg, Diane Fatkin

    Publicado em 2021
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  14. 14
    The Athlete’s Heart—Challenges and Controversies

    The Athlete’s Heart—Challenges and Controversies por André La Gerche, Meagan M. Wasfy, Maria J. Brosnan, Guido Claessen, Diane Fatkin, Hein Heidbüchel, Aaron L. Baggish, Jason C. Kovacic

    Publicado em 2022
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  15. 15
    Reduced Penetrance, Variable Expressivity, and Genetic Heterogeneity of Familial Atrial Septal Defects

    Reduced Penetrance, Variable Expressivity, and Genetic Heterogeneity of Familial Atrial Septal Defects por D. Woodrow Benson, Angela Sharkey, Diane Fatkin, Peter Lang, Craig T. Basson, Barbara McDonough, Arnold W. Strauss, J.G. Seidman, Christine E. Seidman

    Publicado em 1998
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  16. 16
    Complexity of Murine Cardiomyocyte miRNA Biogenesis, Sequence Variant Expression and Function

    Complexity of Murine Cardiomyocyte miRNA Biogenesis, Sequence Variant Expression and Function por David T. Humphreys, Carly J. Hynes, Hardip R. Patel, Grace Wei, L. Edward Cannon, Diane Fatkin, Catherine M. Suter, Jennifer L. Clancy, Thomas Preiß

    Publicado em 2012
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  17. 17
    Pathways of Ca<sup>2+</sup> entry and cytoskeletal damage following eccentric contractions in mouse skeletal muscle

    Pathways of Ca<sup>2+</sup> entry and cytoskeletal damage following eccentric contractions in mouse skeletal muscle por Bao‐Ting Zhang, Nicholas P. Whitehead, Othon Gervásio, Trent F. Reardon, Molly Vale, Diane Fatkin, Alexander Dietrich, Ella W. Yeung, David G. Allen

    Publicado em 2012
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  18. 18
    Familial Dilated Cardiomyopathy Locus Maps to Chromosome 2q31

    Familial Dilated Cardiomyopathy Locus Maps to Chromosome 2q31 por Benjamin L. Siu, Hideshi Niimura, John A. Osborne, Diane Fatkin, Calum A. MacRae, Scott Solomon, D. Woodrow Benson, J.G. Seidman, Christine E. Seidman

    Publicado em 1999
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  19. 19
    Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the α cardiac myosin heavy chain gene

    Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the α cardiac myosin heavy chain gene por Diane Fatkin, Michael E. Christe, Orlando Aristizábal, Bradley K. McConnell, Shardha Srinivasan, Frederick J. Schöen, Christine E. Seidman, Daniel H. Turnbull, Jonathan G. Seidman

    Publicado em 1999
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  20. 20
    Mutation of the LUNATIC FRINGE Gene in Humans Causes Spondylocostal Dysostosis with a Severe Vertebral Phenotype

    Mutation of the LUNATIC FRINGE Gene in Humans Causes Spondylocostal Dysostosis with a Severe Vertebral Phenotype por Duncan B. Sparrow, Gavin Chapman, Merridee A. Wouters, Neil V. Whittock, Sian Ellard, Diane Fatkin, Peter D. Turnpenny, Kenro Kusumi, Daniel J. Sillence, Sally L. Dunwoodie

    Publicado em 2005
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