Výpis publikací

RAUDENSKÁ, Martina, Tomáš NOVOTNÝ, Alexandra BITTNEROVÁ a Anna VAŠKŮ. Mutational Screening of SCN5A in Patients Suspected of LQTS. In European Journal of Heart Failure Supplements 2009; Vol. 8(2). 2009.

RAUDENSKÁ, Martina, Ivo PAPOUŠEK a Karel CHROUST. Mutational Screening of Human Genes which Are Associated with Long QT Syndrome Occurrence. In XI. setkání biochemiků a molekulárních biologů. Česká republika, Brno: Masarykova univerzita, 2007, s. 35-35. ISBN 978-80-210-4234-6.

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.

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.

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.