Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Onur Işık"'
Autor:
Onur Işık
Publikováno v:
Literacy Trek, Vol 7, Iss 2, Pp 105-114 (2021)
Goncourt Prize (2016) awarded Lullaby, a novel based on a real event, by Slimani tells a tragic story that ends with the killing of two children. Although the work seems like a thriller novel at a first glance, it exhibits a reflection of belonging a
Externí odkaz:
https://doaj.org/article/f30807a9b345439e989fc00ffc53b6fc
Publikováno v:
Journal of Cardiovascular and Thoracic Research, Vol 13, Iss 3, Pp 254-257 (2021)
Pulmonary arterial sling (PAS) is a relatively rare congenital anomaly in which left pulmonary artery branch originates abnormally from the right pulmonary artery, eventually resulting with respiratory symptoms, due to airway obstruction. In this rep
Externí odkaz:
https://doaj.org/article/cfd9017f90d74157a6902636bf2d0e3d
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 48, Iss 1, Pp 67-71 (2020)
Scimitar syndrome is a rare congenital heart defect characterized by the combination of vascular, bronchial, and parenchymal malformations. This syndrome includes anomalous right pulmonary venous drainage to the inferior caval vein, hypoplastic right
Externí odkaz:
https://doaj.org/article/5826aa8f04a14fe49b9cf85386f8b20b
Autor:
Onur Işık, Muhammet Akyüz, Engin Karakuş, Esra Işık, Mehmet Fatih Ayık, Ertürk Levent, Yüksel Atay
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 46, Iss 5, Pp 385-391 (2018)
Objective: The aim of this study was to evaluate the efficacy and safety of the Doty surgical approach in pediatric patients with congenital supravalvular aortic stenosis (SVAS) by examining early and mid-term outcomes. Methods: Surgical repair using
Externí odkaz:
https://doaj.org/article/357a91c4f23f4af19f9f0431f1a01132
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 43, Iss 7, Pp 640-643 (2015)
Double-chambered right ventricle is a rare heart defect causing right ventricular outflow tract (RVOT) obstruction. In this malformation, the right ventricle is divided into two chambers by a fibromuscular band. A 12-year old female patient who had u
Externí odkaz:
https://doaj.org/article/793ced135701479fb33b011b95586b18
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 44, Iss 2, Pp 148-150 (2016)
Cor triatriatum sinister is a rare congenital cardiac pathology, representing only 0.1% of congenital cardiac anomalies, and often associated with other cardiac defects. In classic cor triatriatum sinister, the pulmonary venous chamber receives all p
Externí odkaz:
https://doaj.org/article/8f36c85455c449f7ac57890b266f8908
Publikováno v:
Journal of Surgery and Medicine. 6:939-942
Background/Aim: Parallel to the developments in congenital heart surgery, the number of children undergoing resternotomy (redo) heart surgery is increasing. In this specific group of patients, post-operative pneumothorax (PTX) and atelectasis are pre
Autor:
Doga Luleyap, Aysenur O. Dogruoz, Ali Rahmi Bakiler, Fatih Durak, Ilker Mercan, Onur Işık, Ayse Berna Anil, Belde K. Demir, Eda Karadag Oncel, Capan Konca, Muhammed Akyuz, Emine Pinar Küllüoglu
Publikováno v:
Journal of Pediatric Infectious Diseases. 17:053-058
Multisystem inflammatory syndrome in children (MIS-C) is a severe disease that can lead to death. There is no definitive treatment for MIS-C yet. It has been reported that intravenous immunoglobulin, intravenous methylprednisolone, fluid supplements,
Publikováno v:
General Thoracic and Cardiovascular Surgery. 69:1527-1531
The mini-sternotomy has become a common approach of choice for a wide range of congenital defects requiring minimally invasive surgery. Here, we aimed to present closed heart surgery results via limited upper mini-sternotomy in the newborn and infant
Publikováno v:
Journal of Cardiovascular and Thoracic Research
Journal of Cardiovascular and Thoracic Research, Vol 13, Iss 3, Pp 254-257 (2021)
Journal of Cardiovascular and Thoracic Research, Vol 13, Iss 3, Pp 254-257 (2021)
Pulmonary arterial sling (PAS) is a relatively rare congenital anomaly in which left pulmonary artery branch originates abnormally from the right pulmonary artery, eventually resulting with respiratory symptoms, due to airway obstruction. In this rep