Hasil Pencarian - A. Graham Stuart

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  1. 1
    Functional and pharmacological characterization of an S5 domain hERG mutation associated with short QT syndrome

    Functional and pharmacological characterization of an S5 domain hERG mutation associated with short QT syndrome oleh Andrew Butler, Yihong Zhang, A. Graham Stuart, Christopher E. Dempsey, Jules C. Hancox

    Diterbitkan 2019-04-01
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  2. 2
    The Role of Speckle Tracking Echocardiography in the Evaluation of Common Inherited Cardiomyopathies in Children and Adolescents: A Systematic Review

    The Role of Speckle Tracking Echocardiography in the Evaluation of Common Inherited Cardiomyopathies in Children and Adolescents: A Systematic Review oleh Dan M. Dorobantu, Curtis A. Wadey, Nurul H. Amir, A. Graham Stuart, Craig A. Williams, Guido E. Pieles

    Diterbitkan 2021-04-01
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  3. 3
    Percentage Predicted Peak Oxygen Consumption in People With Fontan Circulation: A Rapid Systematic Scoping Review and Validation Study

    Percentage Predicted Peak Oxygen Consumption in People With Fontan Circulation: A Rapid Systematic Scoping Review and Validation Study oleh Curtis A. Wadey, Owen W. Tomlinson, Alan R. Barker, A. Graham Stuart, Derek L. Tran, Karina Laohachai, Julian Ayer, Robert G. Weintraub, Rachael Cordina, Craig A. Williams

    Diterbitkan 2024-09-01
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  4. 4
    Functionally significant, rare transcription factor variants in tetralogy of Fallot.

    Functionally significant, rare transcription factor variants in tetralogy of Fallot. oleh Ana Töpf, Helen R Griffin, Elise Glen, Rachel Soemedi, Danielle L Brown, Darroch Hall, Thahira J Rahman, Jyrki J Eloranta, Christoph Jüngst, A Graham Stuart, John O'Sullivan, Bernard D Keavney, Judith A Goodship

    Diterbitkan 2014-01-01
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  5. 5
    2020 ESC Guidelines on sports cardiology and exercise in patients with cardiovascular disease

    2020 ESC Guidelines on sports cardiology and exercise in patients with cardiovascular disease oleh Antonio Pelliccia, Sanjay Sharma, Sabiha Gati, Maria Bäck, Mats Börjesson, Stefano Caselli, Jean-Philippe Collet, Domenico Corrado, Jonathan A. Drezner, Martin Halle, Dominique Hansen, Hein Heidbuchel, Jonathan Myers, Josef Niebauer, Michael Papadakis, Massimo Francesco Piepoli, Eva Prescott, Jolien W. RoosHesselink, A. Graham Stuart, Rod S. Taylor, Paul D. Thompson, Monica Tiberi, Luc Vanhees, Matthias Wilhelm

    Diterbitkan 2021-06-01
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  6. 6
    Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation.

    Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation. oleh Helen R Griffin, Darroch H Hall, Ana Topf, James Eden, A Graham Stuart, Jonathan Parsons, Ian Peart, John E Deanfield, John O'Sullivan, Sonya V Babu-Narayan, Michael A Gatzoulis, Frances A Bu'lock, Shoumo Bhattacharya, Jamie Bentham, Martin Farrall, Javier Granados Riveron, J David Brook, John Burn, Heather J Cordell, Judith A Goodship, Bernard Keavney

    Diterbitkan 2009-01-01
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