Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Nazan, Özbarlas"'
Autor:
Fadli Demir, Tolga Akbaş, Sevcan Erdem, Berivan Subaşı, Celal Varan, Orhan Kemal Salih, Nazan Özbarlas
Publikováno v:
Turkish Journal of Thoracic and Cardiovascular Surgery. 31:19-28
Background: The aim of the study was to evaluate the clinical and diagnostic findings, treatment, and follow-up of cases of anomalous origin of coronary arteries from the pulmonary artery. Methods: Between January 1998 and June 2021, a total of 14 pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60831369014d54481abc38a778a04550
https://doi.org/10.5606/tgkdc.dergisi.2023.23396
https://doi.org/10.5606/tgkdc.dergisi.2023.23396
Publikováno v:
Cukurova Medical Journal, Vol 43, Iss 4, Pp 1015-1022 (2018)
Amaç: Çalışmamızda kronik böbrek yetersizliği nedeniyle hemodiyaliz yapılan hastalarda hemodiyaliz öncesi ve sonrası kardiyak fonksiyonların değerlendirilmesi planlanmıştır. Gereç ve Yöntem: Çalışmaya altı aydan daha uzun süredi
Externí odkaz:
https://doaj.org/article/bc4d54ec0e434146ae76d5cf830f349a
Publikováno v:
The Anatolian Journal of Cardiology. 26:702-709
The aim of this study is to review the spectrum of the prenatally detected absent pulmonary valve syndrome and its outcome after diagnosis.Clinical data and echocardiographic findings of 37 cases with a fetal diagnosis of absent pulmonary valve syndr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40a614130451da056911d2ebd34c9adf
https://doi.org/10.5152/anatoljcardiol.2022.1461
https://doi.org/10.5152/anatoljcardiol.2022.1461
Perkütan kapatmaya şiddetli pulmoner hipertansiyonu olan patent duktus arteriozusda şans verilebilir
Publikováno v:
Cukurova Medical Journal, Vol 45, Iss 2, Pp 758-759 (2020)
Externí odkaz:
https://doaj.org/article/a79c87cde62f4a238423444351f64d69
Publikováno v:
Cukurova Medical Journal, Vol 41, Iss 1, Pp 47-50 (2016)
Purpose: Long QT Syndrome (LQTS) is characterized by prolonged ventricular repolarization and tendency to malignant tachyarrhythmia. We reported 16 patient diagnosed congenitally LQTS as a tertiary centre's 12 years experience. Material and Methods:
Externí odkaz:
https://doaj.org/article/cc7eaeceddd84bba80ac3552efad4666
Autor:
Fadli Demir, Celal Varan, Sevcan Erdem, Anıl Atmış, Tolga Akbaş, Berivan Subaşı, Yasin Güzel, Nazan Özbarlas
Publikováno v:
Cardiology in the young.
The aim of this study was to present the clinical and microbiological characteristics of patients with infective endocarditis. A retrospective evaluation was made of patients diagnosed with infective endocarditis between 1995 and 2021. The clinical a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26d8d25a81f040668d653f5c4b4e9430
https://pubmed.ncbi.nlm.nih.gov/36419327
https://pubmed.ncbi.nlm.nih.gov/36419327
Publikováno v:
Cukurova Medical Journal, Vol 41, Iss 2, Pp 393-395 (2016)
Cardiorenal syndrome is a disorder of the heart and kidneys in which acute or chronic dysfunction in one organ may induce acute or chronic dysfunction in the other organ. It is well known that the main cause of mortality among patients with end-stage
Externí odkaz:
https://doaj.org/article/9e3ccdb927f04eb2b29e5611f0b381fb
Publikováno v:
Cogent Medicine, Vol 3, Iss 1 (2016)
Congenital heart disease (CHD) is the most common congenital birth defect, and hypoplastic left heart syndrome (HLHS) is a relatively common form of CHD, with an estimated incidence of 0.1–0.25 per 1,000 live births. However, twin pregnancies in wh
Externí odkaz:
https://doaj.org/article/2a5801f4161c49fa8d48189e601546d4
Autor:
Oğuz Canan, Osman Küçükosmanoğlu, Fadli Demir, Alev Arslan, Nazan Özbarlas, Sevcan Erdem, Mustafa Ayana, Yankı Kaan Okuducu
Publikováno v:
Cardiology in the Young. 30:1086-1094
This study evaluates clinical and epidemiological features of acute rheumatic fever using the data of last 25 years in our hospital in south-east of Turkey. The medical records of 377 patients with acute rheumatic fever admitted to Pediatric Cardiolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bda35205400e87495431b790f46b1491
https://doi.org/10.1017/s1047951120001596
https://doi.org/10.1017/s1047951120001596
Autor:
Selim Büyükkurt, Tolga Akbaş, Berivan Çağnıs, Fadli Demir, Nazan Özbarlas, Ferda Özlü, Sevcan Erdem
Publikováno v:
Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology. 42(5)
Isolated restrictive foramen ovale (rFO) without complex heart defects is a rare pathology. There may be difficulties in managing this situation, which can lead to right heart enlargement, tricuspid regurgitation and hydrops findings in the foetus. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::411bdfa988a5d4006814fa74b3f9a0cc
https://pubmed.ncbi.nlm.nih.gov/34704528
https://pubmed.ncbi.nlm.nih.gov/34704528