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dc.contributor.authorOzkara, A
dc.contributor.authorYildiz, CE
dc.contributor.authorCetin, G
dc.contributor.authorSaltik, L
dc.contributor.authorBakir, I
dc.contributor.authorMert, M
dc.contributor.authorPaker, T
dc.contributor.authorAkcevin, A
dc.date.accessioned2021-03-05T09:11:43Z
dc.date.available2021-03-05T09:11:43Z
dc.date.issued2004
dc.identifier.citationMert M., Paker T., Akcevin A., Cetin G., Ozkara A., Saltik L., Bakir I., Yildiz C., "Diagnosis, management, and results of treatment for aortopulmonary window", CARDIOLOGY IN THE YOUNG, cilt.14, ss.506-511, 2004
dc.identifier.issn1047-9511
dc.identifier.otherav_9cbc47fc-3bd1-41bb-a8c5-85ee0df32dae
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/105322
dc.identifier.urihttps://doi.org/10.1017/s1047951104005074
dc.description.abstractThe aortopulmonary window is a communication between the ascending aorta and the pulmonary trunk in the presence of two separate arterial valves. This uncommon congenital anomaly is reported rarely in the literature. We present here our experience with 16 patients, emphasizing the importance of early closure of the defect by a transaortic approach.
dc.language.isoeng
dc.subjectKardiyoloji
dc.subjectTıp
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectPEDİATRİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectCARDIAC ve CARDIOVASCULAR SİSTEMLER
dc.titleDiagnosis, management, and results of treatment for aortopulmonary window
dc.typeMakale
dc.relation.journalCARDIOLOGY IN THE YOUNG
dc.contributor.department, ,
dc.identifier.volume14
dc.identifier.issue5
dc.identifier.startpage506
dc.identifier.endpage511
dc.contributor.firstauthorID101935


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