Zobrazeno 1 - 10
of 73
pro vyhledávání: '"A. Rahmi Bakiler"'
Autor:
Tülay Demircan, Barış Güven, Ali Rahmi Bakiler, Halil Gürsoy Pala, Ayşe Şimşek, Nazmi Narin, Cem Karadeniz
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 12, Iss 1, Pp 1-5 (2022)
Objective: The aim of this study was to analyze the frequency and results of congenital heart defects (CHD) in multipl pregnancies by fetal echocardiography. Among these, to evaluate critical congenital heart diseases such as hypoplastic left heart s
Externí odkaz:
https://doaj.org/article/199eb79fd8c342c9b1eda67d031d2e95
Publikováno v:
In Archives de pédiatrie April 2020 27(3):140-145
Autor:
Yüksel Bıcılıoğlu, Murat Anıl, Gamze Gökalp, Emel Ataş Berksoy, Gülberat İnce, Ali Rahmi Bakiler
Publikováno v:
Journal of Pediatric Emergency and Intensive Care Medicine, Vol 7, Iss 1, Pp 13-18 (2020)
Introduction:Supraventricular tachycardia is the most common cause of arrhythmia in children. The aim of this study was to determine the dose and efficacy of adenosine treatment in the management of supraventricular tachycardia and to determine the f
Externí odkaz:
https://doaj.org/article/d133897be6a04f448faf028569d185af
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 10, Iss 1, Pp 71-76 (2020)
INTRODUCTION: There is no established current algorithm of treatment and clinical follow-up in children with coronary artery anomalies. We analysed the clinical characteristics, diagnosis treatment options of children and adolescents identified with
Externí odkaz:
https://doaj.org/article/732e537ac65e41829219db49ad54bbd9
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:
Nurullah Bolat, Kayi Eliacik, Mesut Yavuz, Ali Kanik, Hilal Mertek, Baris Guven, Buket Dogrusoz, Ali Rahmi Bakiler
Publikováno v:
Psychiatry and Clinical Psychopharmacology, Vol 29, Iss 4, Pp 487-491 (2019)
OBJECTIVES: Psychological factors may be the underlying causes in unexplained chest pain (UCP). Chest pain symptom may influence the emotional status and peer relationships of the children and adolescents negatively. However, the number of studies fo
Externí odkaz:
https://doaj.org/article/b7cc9da3d2ff437eb23df7c2ba5637c0
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,
Autor:
Barış Güven, Cem Karadeniz, Muhammet Ali Kanik, Hacer Örsdemir Hortu, Özlem Üzüm, Tülay Demircan, Ali Rahmi Bakiler, Kayı Eliaçık, Emine Nursel Akmaz, Mehmet Helvaci, Yavuz Demirçelik
Publikováno v:
Volume: 38, Issue: 3 241-245
Journal of Experimental and Clinical Medicine
Journal of Experimental and Clinical Medicine
Chest pain is highly prevalent in adolescence, represents a considerable burden for health services, and rarely associated with cardiac disease. Since psychosocial factors are related to chest pain there is a need for exploring the accompanying famil
Publikováno v:
Journal of Pediatric Emergency and Intensive Care Medicine, Vol 7, Iss 1, Pp 13-18 (2020)
Introduction:Supraventricular tachycardia is the most common cause of arrhythmia in children. The aim of this study was to determine the dose and efficacy of adenosine treatment in the management of supraventricular tachycardia and to determine the f
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 41, Iss 5, Pp 448-450 (2013)
Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital anomaly and one of the causes of myocardial ischemia. It often presents with atypical signs and symptoms, especially in childhood. In this case repor
Externí odkaz:
https://doaj.org/article/3adaa131cec3459c9305a11a7c7c6fa4