Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Cansaran Tanidir"'
Autor:
Dinu Antony, Elif Gulec Yilmaz, Alper Gezdirici, Lennart Slagter, Zeineb Bakey, Helen Bornaun, Ibrahim Cansaran Tanidir, Tran Van Dinh, Han G. Brunner, Peter Walentek, Sebastian J. Arnold, Rolf Backofen, Miriam Schmidts
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Laterality defects are defined by the perturbed left–right arrangement of organs in the body, occurring in a syndromal or isolated fashion. In humans, primary ciliary dyskinesia (PCD) is a frequent underlying condition of defective left–right pat
Externí odkaz:
https://doaj.org/article/4e48fa0a6a1249bf9f4769be2632b89b
Autor:
Erkut Ozturk, Ibrahim Cansaran Tanidir, Mustafa Gunes, Serhat Bahadır Genç, Okan Yildiz, Ismihan Selen Onan, Sertac Haydin, Alper Guzeltas
Publikováno v:
İstanbul Kuzey Klinikleri, Vol 7, Iss 4, Pp 329-334 (2020)
OBJECTIVE: The effects of Vasoactive-Ventilation-Renal (VVR) score on the evaluation of pediatric heart surgery results were investigated in this study. METHODS: This retrospective study included children younger than 18 years of age who were operate
Externí odkaz:
https://doaj.org/article/56e95b51de7c4ec495b068663add4ac4
Autor:
Taner Kasar, Ozturk Erkut, İ. Cansaran Tanidir, Murat Şahin, M. Akin Topkarci, Alper Guzeltas
Publikováno v:
Medicine. 101(51)
Although balloon-expandable stent implantation for native aortic coarctation is a preferred method in the adolescent age group, there are insufficient data about indications for and the efficacy of the procedure in a younger age group. The aim of thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d72aa9d93bce4bbb02c5b1a162a0381c
https://pubmed.ncbi.nlm.nih.gov/36595787
https://pubmed.ncbi.nlm.nih.gov/36595787
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 43, Iss 2, Pp 192-195 (2015)
Scimitar syndrome is a rare disease associated with a right lung sequestration vascularised by arteries arising from the abdominal aorta and abnormal venous drainage into the inferior vena cava. The infantile form is generally presented with severe h
Externí odkaz:
https://doaj.org/article/cebd62e982af43119abefc8848ec11d4
Autor:
Ismihan Selen Onan, Pelin Ayyıldız, Erkut Öztürk, Cagdas Topel, Alper Güzeltaş, Ibrahim Cansaran Tanidir, Sertaç Haydin, Aysel Türkvatan, Hacer Kamalı
Publikováno v:
Revista Portuguesa de Cardiologia, Vol 40, Iss 8, Pp 583-590 (2021)
Revista Portuguesa de Cardiologia (English Edition), Vol 40, Iss 8, Pp 583-590 (2021)
Revista Portuguesa de Cardiologia (English Edition), Vol 40, Iss 8, Pp 583-590 (2021)
Introduction: Echocardiography (echo) is the primary non-invasive imaging modality for the assessment of congenital heart disease (CHD). Computed tomography angiography (CTA) also has potential to examine the anatomy of complex heart anomalies as wel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::558cb9260650eb34098e36d488fb5720
https://doi.org/10.1016/j.repce.2020.12.017
https://doi.org/10.1016/j.repce.2020.12.017
Publikováno v:
Diagn Interv Radiol
Diagnostic and Interventional Radiology
Diagnostic and Interventional Radiology
Purpose: this study was planned to assess the application of three-dimensional (3D) cardiac modeling in preoperative evaluation for complex congenital heart surgeries. Methods: from July 2015 to September 2019, 18 children diagnosed with complex cong
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2377eeeacde069aa2300c8f1e23e061e
https://doi.org/10.5152/dir.2021.20163
https://doi.org/10.5152/dir.2021.20163
Autor:
İsmihan Selen Onan, Gülhan Tunca Şahin, Ibrahim Cansaran Tanidir, Yakup Ergül, Hasan Candaş Kafalı, Alper Güzeltaş, Erkut Öztürk, Sertaç Haydin
Publikováno v:
Turkish Journal of Thoracic and Cardiovascular Surgery
Background This study aims to evaluate early postoperative arrhythmias in children undergoing congenital cardiac surgery. Methods A total of 670 pediatric patients (355 males, 315 females; median age: 4 months; range, 1 day to 18 years) who underwent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e08a46824564f40de5c49798890a805f
https://doi.org/10.5606/tgkdc.dergisi.2021.20366
https://doi.org/10.5606/tgkdc.dergisi.2021.20366
Autor:
Okan Yildiz, Alper Güzeltaş, Pelin Ayyıldız, Erkut Öztürk, Yakup Ergül, Mustafa Güneş, Halil Sencer Akdeniz, Hasan Candaş Kafalı, Fatma Sevinç Şengül, Ibrahim Cansaran Tanidir, Sertaç Haydin
Publikováno v:
Cardiology in the Young. 31:940-948
Objectives:In recent years, cardiac resynchronization therapy (CRT) has also started to be performed in the paediatric and CHD population. This study aimed to evaluate the efficacy of CRT in children with CHD.Patients and methods:Patients with CHD wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd0dbfa4ef46927f966289b82d4aa93b
https://doi.org/10.1017/s1047951120004795
https://doi.org/10.1017/s1047951120004795
Autor:
Servet Ergün, Serhat Bahadır Genç, Ismihan Selen Onan, Erman Cilsal, Sertaç Haydin, Okan Yildiz, Ibrahim Cansaran Tanidir, Alper Güzeltaş
Publikováno v:
Pediatric Cardiology. 42:840-848
We investigated the effects of intraoperative parameters measured during pulmonary artery banding operations and pre-discharge parameters on the completion of Fontan procedures. Fifty consecutive patients with single-ventricle anomalies and unrestric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce42b6436305f4c6fbde9691bf848dbf
https://doi.org/10.1007/s00246-021-02548-7
https://doi.org/10.1007/s00246-021-02548-7
Publikováno v:
Echocardiography. 38:114-117
Topsy-turvy heart is a rare congenital anomaly; it has a specific characteristic of cardiac malrotation and superior-inferior arrangement of right/left ventricles. A five-day-old patient was diagnosed antenatally with hypoplastic left heart and right
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3ac3d2de71dd98470501734c4d38ee8a
https://doi.org/10.1111/echo.14950
https://doi.org/10.1111/echo.14950