Zobrazeno 1 - 10
of 102
pro vyhledávání: '"Senem, Özgür"'
Autor:
Hanife Saat, Ibrahim Şahin, Haktan Bagğış Erdem, Senem Özgür, Semiha Terlemez Tokgöz, Taha Bahsi&775;
Publikováno v:
Anatolian Journal of Cardiology, Vol 26, Iss 6, Pp 460-465 (2022)
Background: Hereditary cardiac arrhythmias result from mutations in various genes encoding ion channels. One major channelopathy is long QT syndrome, which has excel-lent genetic and clinical heterogeneity. Arrhythmogenic right ventricular cardiomyop
Externí odkaz:
https://doaj.org/article/8873e398e5f145cbb506ecbe9ab65041
Autor:
Yakup Ergül, Gülhan Tunca Şahin, Hasan Candaş Kafalı, Erkut Öztürk, Senem Özgür, Sertaç Haydin, Alper Güzeltaş
Publikováno v:
Anatolian Journal of Cardiology, Vol 25, Iss 4, Pp 250-257 (2021)
Externí odkaz:
https://doaj.org/article/97bf9e565bcf43f9ab6544eb6cf0a1df
Autor:
Hasan Candaş Kafalı, Erkut Öztürk, Senem Özgür, Gülhan Tunca Şahin, Alper Güzeltaş, Yakup Ergül
Publikováno v:
Anatolian Journal of Cardiology, Vol 24, Iss 6, Pp 370-376 (2020)
Objective: The aim of this study is to present electrophysiologic characteristics and catheter ablation results of tachycardia-induced cardiomyopathy (TIC) in children with structurally normal heart. Methods: We performed a single-center retrospectiv
Externí odkaz:
https://doaj.org/article/6167fbacae21420287efe085a648d43c
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 48, Iss 2, Pp 171-176 (2020)
Ventricular arrhythmias arising from coronary cusps are not uncommon. However, the mapping and ablation of outflow tract ventricular arrhythmias originating from aortic cusps can be challenging. Radiofrequency ablation of this area can cause rare but
Externí odkaz:
https://doaj.org/article/7d98e0c1d6934bc5aa1b2efda7867fb9
Autor:
Fatma Sevinç Şengül, Gülhan Tunca Şahin, Senem Özgür, Hasan Candaş Kafalı, Okan Akıncı, Alper Güzeltaş, Yakup Ergül
Publikováno v:
Anatolian Journal of Cardiology, Vol 22, Iss 2, Pp 60-67 (2019)
Objective: Arrhythmogenic right ventricular dysplasia (ARVD) is a myocardial genetic disease that occurs primarily in the right ventricle. Patients with ARVD may present with severe ventricular arrhythmias, syncope, and cardiac arrest. The purpose of
Externí odkaz:
https://doaj.org/article/5e943d99864e4933a8cfa2a4dc4d5981
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 9, Iss 2, Pp 87-92 (2019)
INTRODUCTION: We aimed to determine the prevalence of aortic arch anomalies in children who underwent cardiac catheterization and angiography for various reasons. METHODS: 1928 patients who underwent diagnostic or interventional cardiac catheterizati
Externí odkaz:
https://doaj.org/article/7dd00406c5bb4e95b22341c5fcccf1de
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 46, Iss 8, Pp 718-722 (2018)
Andersen-Tawil syndrome (ATS) is a disorder that causes episodes of muscle weakness (periodic paralysis), changes in heart rhythm, and developmental abnormalities. QT prolongation and ventricular arrhythmias, including bidirectional ventricular tachy
Externí odkaz:
https://doaj.org/article/37ce2ed10896435eaf263d75a6ee68f3
Autor:
Rumeysa Çitli, Seda Aydoğan, Nurdan Dinlen Fettah, Dilek Dilli, Utku Arman Örün, Hasan Akduman, Serpil Kaya Çelebi, Ayşegül Zenciroğlu, Senem Özgür, Başak Kaya Gürsoy
Publikováno v:
Dicle Medical Journal, Vol 48, Iss 4, Pp 662-668 (2021)
Volume: 48, Issue: 4 662-668
Dicle Tıp Dergisi
Volume: 48, Issue: 4 662-668
Dicle Tıp Dergisi
Objective: Supraventricular tachycardia, one of the most common conditions requiring emergency cardiac intervention in newborns, is also the most common symptomatic tachyarrhythmia in newborns. Therefore, early diagnosis and treatment approach is imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84f26a330f3f27daa6f68e73822f9224
https://doi.org/10.5798/dicletip.1001875
https://doi.org/10.5798/dicletip.1001875
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 42, Iss 2, Pp 190-193 (2014)
Double outlet right ventricle is a cardiac malformation in which both the aorta and pulmonary artery arise from the right ventricle. A double outlet right ventricle with intact ventricular septum is extremely rare. A nine-day-old boy born at 38 weeks
Externí odkaz:
https://doaj.org/article/4f43878facec43e28e3efe606aa156b2
Publikováno v:
Turkiye Klinikleri Journal of Pediatrics. 30:22-30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30ad45b05a3a18e6af99998ed4f5e099
https://doi.org/10.5336/pediatr.2020-75455
https://doi.org/10.5336/pediatr.2020-75455