Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Kaan Yıldız"'
Autor:
Erkan Çağlıyan, Samican Ozmen, Süreyya Sarıdaş Demir, Aslı Akdöner, Sabahattin Altunyurt, Burak Deliloglu, Kaan Yıldız, Halise Zeynep Genç, Mustafa Kır
Publikováno v:
Forbes Tıp Dergisi, Vol 1, Iss 2, Pp 42-50 (2020)
INTRODUCTION: Evidence shows that rather than postnatal diagnoses, prenatal diagnoses of congenital heart diseases are correlated with better long-term results and lower mortality rates. In this retrospective study, neonatal stage results of infants
Externí odkaz:
https://doaj.org/article/d59b09e64185423aae54ecb2a14b1460
Autor:
Kaan Yıldız, Yasin Ertuğ Çekdemir, Muhammet Salman, Mustafa Kır, Handan Güleryüz, Öztekin Oto, Nurettin Ünal
Publikováno v:
e-Journal of Cardiovascular Medicine. 11:23-30
Objectives: In this study, a comparison of cardiac magnetic resonance imaging (MRI) and simultaneous transthoracic echocardiography data were obtained from patients with great artery transposition (TGA), who underwent arterial switch operation (ASO)
Publikováno v:
e-Journal of Cardiovascular Medicine. 10:144-147
Publikováno v:
Turkish Journal of Thoracic and Cardiovascular Surgery
Ectopia cordis is a rare congenital disorder in which the heart is partially or completely located outside the chest cavity. In this article, we present four cases of ectopia cordis accompanied by cardiac abnormalities with either thoracic and/or abd
Autor:
Murat Kaan Yıldız
Publikováno v:
The Legends Avrupa Tarihi Çalışmaları Dergisi. 2:106-129
Autor:
Erdener Özer, Nurettin Ünal, Öztekin Oto, Şebnem Paytoncu, Halise Zeynep Genc, Mustafa Kir, Resmiye Irmak Yuzuguldu, Kaan Yıldız
Inflammatory myofibroblastic tumor (IMT) is a rare soft tissue tumor of the heart. In the literature, cardiac IMT is often described as an endocardial-based cavitary mass originating from the right side of the heart in infants and adolescents. In thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cecee49e0069710015a3786fbd3e7e4b
https://avesis.deu.edu.tr/publication/details/b0bba343-3190-4703-836e-04775e187406/oai
https://avesis.deu.edu.tr/publication/details/b0bba343-3190-4703-836e-04775e187406/oai
Autor:
Ayşe Şimşek, Tulay Demircan, Fatma Sarioğlu, Sedat Bağlı, Engin Gerçeker, Kaan Yıldız, cem karadeniz, Nazmi Narin
Levoatrial cardinal vein (LACV) is anomalous connection between the left atrium or pulmonary veins and any systemic vein which is derived from cardinal venous system. Presence of the levoatrial cardinal vein without a cardiac anomaly is a very rare c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47a2956d2cc5146c7aa0489e914bd09d
https://doi.org/10.22541/au.163260371.15847463/v1
https://doi.org/10.22541/au.163260371.15847463/v1
Autor:
Samican Özmen, Kaan Yıldız, Aslı Akdöner, Halise Zeynep Genc, Sabahattin Altunyurt, Burak Deliloğlu, Mustafa Kir, Erkan Çağliyan, Süreyya Saridaş
Publikováno v:
Forbes Journal of Medicine.
INTRODUCTION: Evidence shows that rather than postnatal diagnoses, prenatal diagnoses of congenital heart diseases are correlated with better long-term results and lower mortality rates. In this retrospective study, neonatal stage results of infants
Publikováno v:
Poster Presentations.
Background Kawasaki Disease (KD) is an acute, systemic, febrile vasculitis that occurs during infancy and is the most common cause of childhood coronary artery disease. The incidence of coronary artery lesions (CALs) has declined with the routine use
Autor:
Kaan Yildiz, Nazmi Narin, Sedef Oksuz, Rahmi Ozdemir, Ozge Pamukcu, Ali Baykan, Abdullah Ozyurt, Sedat Bagli, Rasit Aktas, Ikbal Nur Safak, Muhammed Akif Atlan, Yunus Sezer Bayam, Cem Karadeniz
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
IntroductionDevice closure of perimembranous ventricular septal defects (pmVSD) is a successful off-label treatment alternative. We aim to report and compare the outcomes of pmVSD closure in children weighing less than 10 kg using Amplatzer Duct Occl
Externí odkaz:
https://doaj.org/article/972ca847ecbc4916805f8b3460ce4c04