Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Türkay Sarıtaş"'
Autor:
Hacer Kamalı, Özlem Sivaslı Gül, Senay Çoban, Gizem Sarı, Türkay Sarıtaş, Abdullah Erdem, Bedri Aldudak
Publikováno v:
Anatolian Journal of Cardiology, Vol 26, Iss 4, Pp 276-285 (2022)
Background: Transcatheter closure of perimembraneous ventricular septal defect still poses a challenge due to the adjacent structures of the tricuspid and aortic valves and the risk of atrioventricular block. We report our experience at 2 centers usi
Externí odkaz:
https://doaj.org/article/6087fcf3634d46fbbb5f9272672ac9bb
Autor:
İbrahim Halil Demir, Abdullah Erdem, Türkay Sarıtaş, Fadli Demir, Nurdan Erol, İlker Kemal Yücel, Ahmet Çelebi, Numan Ali Aydemir
Publikováno v:
Balkan Medical Journal, Vol 30, Iss 2, Pp 191-196 (2013)
Background: Aortopulmonary window (APW) is a communication between the ascending aorta and the pulmonary artery in the presence of two separate semilunar valves and is the rarest of septal defects. Aims: To present our experience with the diagnosi
Externí odkaz:
https://doaj.org/article/5b50bbd3cdaf47468f5e8de5867ae13f
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 43, Iss 5, Pp 498-498 (2015)
Externí odkaz:
https://doaj.org/article/25a51c8f97054cca82ccc65d260cf830
WOS: 000385271000023 Currently, arterial switch operation appears as a standard surgical management for patients under three weeks of age with transposition of the great arteries with an intact ventricular septum, while, beyond three weeks of age, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24a81fce1b4335ad4cb0b3c10a217c1e
https://hdl.handle.net/20.500.12511/539
https://hdl.handle.net/20.500.12511/539
Autor:
Abdullah, Erdem, Numan Ali, Aydemir, Halil, Demir, Cenap, Zeybek, Türkay, Sarıtaş, Celal, Akdeniz, Ali Rıza, Karacı, Ahmet, Celebi
Publikováno v:
Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir. 38(6)
Anomalous origin of one pulmonary artery branch from the aorta in the presence of separate aortic and pulmonary valves is a rare but important entity necessitating early diagnosis and surgery to prevent irreversible vascular pulmonary disease. We eva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::139a1961686a7ec4bb090e0cd22b8286
https://pubmed.ncbi.nlm.nih.gov/21200120
https://pubmed.ncbi.nlm.nih.gov/21200120
Akademický článek
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Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 43, Iss 6, Pp 551-553 (2015)
Anomalous origin of the circumflex coronary artery from the pulmonary artery is a rare congenital coronary anomaly. While it generally follows an asymptomatic course, if undiagnosed it may lead to severe clinical outcomes, including sudden death. The
Externí odkaz:
https://doaj.org/article/15db9def3d614ce58b35538744e47bde
Akademický článek
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