Masarykova univerzita

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Filtrování publikací

    2008

    1. BÉBAROVÁ, Markéta, Tom 0´HARA, Jan GEELEN, Roselie JONGBLOED, Carl TIMMERMANS, Yvonne ARENS, Luz-Maria RODRIGUEZ, Yoram RUDY a Paul VOLDERS. Subepicardial phase 0 block and discontinuous transmural conduction underlie right precordial ST-segment elevation by a SCN5A loss-of-function mutation. American Journal of Physiology - Heart and Circulatory Physiology. 2008, roč. 295, č. 1, s. H48-H58, 10 s. ISSN 0363-6135.

    2007

    1. 0´HARA, Tom, Markéta BÉBAROVÁ, Paul VOLDERS a Yoram RUDY. Bradycardia-induced ST elevation in Brugada syndrome (mutation F2004L in SCN5A) is due to discontinuous conduction, not abnormal repolarization. In Proceedings of Gordon Research Conference on Cardiac Arrhythmia Mechanisms. 2007.
    2. BÉBAROVÁ, Markéta, Tom 0´HARA, Jan GEELEN, Roselie JONGBLOED, Carl TIMMERMANS, Yvonne ARENS, Luz-Maria RODRIGUEZ, Yoram RUDY a Paul VOLDERS. C-terminal SCN5A mutation, F2004L, in Brugada syndrome: new arrhythmogenic concepts. In Physiological Research. 2007. ISSN 0862-8408.
    3. BÉBAROVÁ, Markéta, Tom 0´HARA, Jan GEELEN, Roselie JONGBLOED, Carl TIMMERMANS, Yvonne ARENS, Luz-Maria RODRIGUEZ, Yoram RUDY a Paul VOLDERS. Subepicardial phase-0 block and discontinuous transmural conduction underlie right-precordial ST-segment elevation in Brugada syndrome by a novel C-terminal SCN5A mutation. In Heart Rhythm. 2007. ISSN 1547-5271.

    2006

    1. VOLDERS, Paul, Markéta BÉBAROVÁ, Roselie JONGBLOED, Jan GEELEN, Carl TIMMERMANS, Yvonne ARENS a Luz-Maria RODRIGUEZ. Clinical, genetic and biophysical characterization of three novel SCN5A mutations in patients with Brugada syndrome. In Eur Heart J. 2006. ISSN 0195-668X.
    2. BÉBAROVÁ, Markéta, Roselie JONGBLOED, Jan GEELEN, Carl TIMMERMANS, Yvonne ARENS, Paul VOLDERS a Luz-Maria RODRIGUEZ. Four novel SCN5A mutations in patients with Brugada syndrome. In Pacing and Clinical Electrophysiology. 2006. ISSN 0147-8389.
    3. BÉBAROVÁ, Markéta, Roselie JONGBLOED, Jan GEELEN, Carl TIMMERMANS, Yvonne ARENS, Paul VOLDERS a Luz-Maria RODRIGUEZ. Functional defect of three novel SCN5A mutations in patients with Brugada syndrome. In Program and abstracts: 7th meeting New Frontiers in Basic Cardiovascular Research. 2006.
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