Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Nur Dikmen Yaman"'
Autor:
Ata Niyazi Ecevi̇t, Nur Di̇kmen Yaman, Burcu Arıcı, Zeynep Eyıleten, Bülent Kaya, Mustafa Adnan Uysalel
Publikováno v:
Düzce Tıp Fakültesi Dergisi, Vol 22, Iss 2, Pp 131-133 (2020)
Sol koroner arterin pulmoner arterden orijin alması (ALCAPA) nadir olmakla birlikte, ilk olarak 1866’da tarif edilen bir major konjenital kardiyak anomalidir. Sol koroner arterin direkt aortaya reimplantasyonu ve koroner arter baypas greftleme pro
Externí odkaz:
https://doaj.org/article/adb5c2630a47427ca2cdd4687cdcc794
Publikováno v:
Turkish Journal of Vascular Surgery, Vol 28, Iss 2, Pp 110-2 (2019)
Coarctation of the thoracic aorta is a frequently seen condition and may cause late anastomotic complications after surgical repair, which often necessitates urgent treatment. Endovascular treatment methods in this group seem to be life-saving due to
Externí odkaz:
https://doaj.org/article/ecc298bf0e5b41fd86dda2ec32bdfaca
Autor:
Mehmet Tasar, Nur Dikmen Yaman, Cahit Saricaoglu, Zeynep Eyileten, Bulent Kaya, Adnan Uysalel
Publikováno v:
Case Reports in Vascular Medicine, Vol 2014 (2014)
The use of percutaneous devices is commonplace for the treatment of many congenital heart defects. However, there are some situations where procedure-related complications are encountered and surgical help is required to ameliorate this issue. Vascul
Externí odkaz:
https://doaj.org/article/b5e0f2b212934205a175cab0d67f80d4
Autor:
Rumeysa Çitli, Burcu Arıcı, Senem Özgür, Nur Dikmen Yaman, İlker Ufuk Sayıcı, Mehmet Taşar, Omer Nuri Aksoy, Huseyin Dursin, Aslı Ayaz
Publikováno v:
Cardiology in the Young. 32:702-704
Introduction:Congenital atrioventricular block is diagnosed in uterine life, at birth, or early in life. Atrioventricular blocks can be life threatening immediately at birth so urgent pacemaker implantation techniques are requested. Reasons can be ca
Publikováno v:
Echocardiography. 37:922-925
Intracardiac blood cysts are rare congenital malformations most commonly located in the endocardium of semilunar or atrioventricular valves. They are predominantly seen in infants, especially below 2 months of age, and disappear spontaneously in the
Autor:
Mehmet, Taşar, Nur Dikmen, Yaman, Burcu, Arıcı, Ömer Nuri, Aksoy, Huseyin, Dursin, Aslı, Ayaz, Rümeysa, Citli, Senem, Özgür, İlker Ufuk, Sayıcı
Publikováno v:
Cardiology in the young. 32(5)
Congenital atrioventricular block is diagnosed in uterine life, at birth, or early in life. Atrioventricular blocks can be life threatening immediately at birth so urgent pacemaker implantation techniques are requested. Reasons can be cardiac or non-
Autor:
Tayfun Uçar, Nur Dikmen Yaman, Ercan Tutar, Mehmet Cakici, Tanıl Kendirli, Zeynep Eyileten, Bahadir Inan, Ahmet Rüçhan Akar
Publikováno v:
Perfusion. 37(5)
Short-term mechanical circulatory support can be life-saving in the pediatric population with acute cardiogenic shock (ACS). However, recovery from MCS is a rare entity. MCS options are limited for low-body-weight children in Turkey. Over the last de
Autor:
Zeynep Eyileten, Burcu Arıcı, Ata Niyazi Ecevit, Nur Dikmen Yaman, Bülent Kaya, Mustafa Adnan Uysalel
Publikováno v:
Düzce Tıp Fakültesi Dergisi, Vol 22, Iss 2, Pp 131-133 (2020)
Volume: 22, Issue: 2 131-133
Duzce Medical Journal
Volume: 22, Issue: 2 131-133
Duzce Medical Journal
Sol koroner arterin pulmoner arterden orijin alması (ALCAPA) nadir olmakla birlikte, ilk olarak 1866’da tarif edilen bir major konjenital kardiyak anomalidir. Sol koroner arterin direkt aortaya reimplantasyonu ve koroner arter baypas greftleme pro
Publikováno v:
Cardiology in the young. 30(12)
Congenital Long QT Syndrome (LQTS) is a dangerous arrhythmic disorder that can be diagnosed in children with bradycardia. It is characterised by a prolonged QT interval and torsades de pointes that may cause sudden death. Long QT syndrome is an ion c
Autor:
Nur Dikmen Yaman
Publikováno v:
Cardiovascular Surgery and Interventions. 5:37-39