Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Mehmet Akif Önalan"'
Autor:
Mehmet Akif Önalan, Didem Melis Öztaş, Burcu Bıçakhan, İbrahim Erdinç, Mert Meriç, Ufuk Alpagut, Murat Uğurlucan
Publikováno v:
e-Journal of Cardiovascular Medicine. 11:17-22
Publikováno v:
Turkish Journal of Thoracic and Cardiovascular Surgery. 31:123-127
Wiskott-Aldrich syndrome is an uncommon X-linked inherited disorder related to primary immunodeficiency, infections, eczema, and thrombocytopenia. A 21-year-old male patient with this syndrome underwent descending aortic aneurysm repair at the age of
Autor:
Mehmet Akif, Önalan, Murat, Çiçek, Okan, Yurdakök, Fatih, Özdemir, Kaan, Altunyuva, Ali Ertan, Ulucan, Oktay, Korun, Hüsnü Fırat, Altın, Emine, Hekim Yılmaz, Numan Ali, Aydemir, Ahmet, Şaşmazel
Publikováno v:
The Turkish Journal of Thoracic and Cardiovascular Surgery. 30:536-541
The aim of this study is to present our experience regarding the creation of an aortopulmonary window as the initial palliative procedure.Between February 2016 and February 2021, a total of eight patients (3 males, 5 females; median age: 2 months; ra
Autor:
Bahar Temur, Mehmet Akif Önalan, Ersin Erek, Selim Aydin, Ender Odemis, Dilek Suzan, Ibrahim Demir
Publikováno v:
World Journal for Pediatric and Congenital Heart Surgery. 12:706-714
Objectives Interrupted aortic arch (IAA) includes a broad spectrum of associated anomalies. In this study, we present our surgical management and patient-specific decisions regarding IAA anomalies with early- and mid-term outcomes. Methods The medica
Autor:
Mehmet Akif Önalan, Ahmet Şaşmazel, Oktay Korun, Numan Ali Aydemir, Hüsnü Fırat Altın, Okan Yurdakök, Filiz İzgi Coşkun, Fatih Özdemir, Mustafa Bulut, Murat Çiçek
Publikováno v:
Koşuyolu Heart Journal. 24:58-61
Introduction: There is limited data on totally anomalous pulmonary venous connection (TAPVC) repair results in our country. The aim of this study is to evaluate the early postoperative results of a large series of TAPVC patients operated in our clini
Publikováno v:
Cardiology in the Young
Coronavirus disease 2019 causes respiratory and systemic disease and has led to a sudden epidemic affecting people of all ages. Patients with congenital heart disease represent a high-risk population. In this article, we present a newborn who require
Autor:
Ersin Erek, Alper Dogruoz, Bahar Temur, Mehmet Akif Önalan, İsmet E Emre, Serdar Basgoze, Esra Ozcan, Selim Aydin
Publikováno v:
Cardiology in the Young. 31:1484-1488
Objective:After congenital heart surgery, some patients may need long-term mechanical ventilation because of chronic respiratory failure. In this study, we analysed outcomes of the patients who need tracheostomy and home mechanical ventilation.Method
Publikováno v:
Turkish Journal of Thoracic and Cardiovascular Surgery
Cardiac leiomyosarcoma is an extremely rare tumor with a poor prognosis. An 18-year-old female patient was admitted to our clinic with a left atrial leiomyosarcoma extending to the right lower pulmonary veins. We performed complete tumor excision by
Publikováno v:
Turkish Journal of Thoracic and Cardiovascular Surgery
A complete sternal cleft is a very rare congenital anomaly causing severe respiratory compromise. Surgical reconstruction options are limited, particularly in low birth weight newborns. Herein, we report a case of low birth weight premature newborn w
Autor:
Ender Odemis, Ersin Erek, Bahar Temur, Murat Saygi, Mehmet Akif Önalan, Selim Aydin, Ibrahim Demir
Publikováno v:
Cardiology in the Young. 30:1772-1782
Objective:We aimed to determine the early and midterm outcomes of ductal stenting in neonates with ductal-dependent pulmonary blood flow.Methods:Between January, 2014 and July, 2018, 102 patients who underwent 115 cardiac catheterisation procedures f