Yeliz Guler
Research Subjects
Yeliz Guler has a total of 18 co-authors. Here are the top co-authors by number of shared publications:
A Guler
Koşuyolu Heart, Education & Research Hospital, Cardiology Clinic, Istanbul-TR, Turkey
1 shared publicationAlev Kilicgedik
1 shared publicationAli M. Esen
Koşuyolu Heart, Education &Research Hospital, Cardiology Clinic, Istanbul, Turkey
1 shared publicationAli Metin Esen
1 shared publicationAm Esen
Koşuyolu Heart, Education & Research Hospital, Cardiology Clinic, Istanbul-TR, Turkey
1 shared publicationAnil Avci
1 shared publication
Latest Publications
- 1 March 2014
- Published by Elsevier in International Journal of Cardiology
- Vol. 172 (2) , e324-e325
An extremely rare trigger of Kounis syndrome: Actinidia chinensis
- 1 March 2014
- Published by Elsevier in International Journal of Cardiology
- Vol. 172 (2) , e324-e325
An extremely rare trigger of Kounis syndrome: Actinidia chinensis
- 26 November 2013
- Published by SAGE Publications in Perfusion
- Vol. 29 (3) , 238-241
Complete A-V block: incidental or a part of cor triatriatum dexter
Cor triatriatum dexter (CTD) is an extremely rare cardiac anomaly in which the right atrium is divided into two distinct chambers by a membrane. The persistence of the right valve of sinus venosus results in a complete septation of the right atrium. This anomaly is frequently associated with other right-sided cardiac abnormalities. Its clinical manifestation and the need for intervention are determined by the number and the size of the fenestrations on the membrane, associated cardiac anomalies and arrhythmias. We describe a case of CTD in a patient with complete atrioventricular (A-V) block.
- 26 November 2013
- Published by SAGE Publications in Perfusion
- Vol. 29 (3) , 238-241
Complete A-V block: incidental or a part of cor triatriatum dexter
Cor triatriatum dexter (CTD) is an extremely rare cardiac anomaly in which the right atrium is divided into two distinct chambers by a membrane. The persistence of the right valve of sinus venosus results in a complete septation of the right atrium. This anomaly is frequently associated with other right-sided cardiac abnormalities. Its clinical manifestation and the need for intervention are determined by the number and the size of the fenestrations on the membrane, associated cardiac anomalies and arrhythmias. We describe a case of CTD in a patient with complete atrioventricular (A-V) block.