Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Osman Güvenç"'
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 45, Iss 5, Pp 454-457 (2017)
Carpenter syndrome (Acrocephalopolysyndactyly type 2, OMIM 201000) is a rarely seen autosomal recessive disorder. In addition to abnormalities such as acrocephaly, craniosynostosis, facial asymmetry, polydactyly and syndactyly, obesity, hypogonadism,
Externí odkaz:
https://doaj.org/article/e31eb83b7436445b81e11101f50d200b
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 45, Iss 4, Pp 373-376 (2017)
Patients with wide patent ductus arteriosus and significant pulmonary hypertension not treated in time constitute a significant problem for cardiologists. For these patients, tests that could aid in decision-making for further planning include revers
Externí odkaz:
https://doaj.org/article/b3a623b354d4448a90ba047ac0fbc840
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 44, Iss 6, Pp 503-506 (2016)
Summary– Jeune syndrome (Asphyxiating thoracic dysplasia) is a rare dystrophy of the skeleton, inherited as an autosomal recessive condition. Patients develop a narrowed thorax, rhizomelic dwarfism, and hepatic, renal, and pancreatic abnormalities.
Externí odkaz:
https://doaj.org/article/f30c1c6e3f5f490d9c76d726f66e70c1
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 45, Iss 6, Pp 538-540 (2017)
Pulmonary arteriovenous malformation, which is defined as the presence of an ab-normal connection between the pulmonary artery and pulmonary vein, is rarely seen. Although it generally presents as a congenital condition, it may be accompanied by here
Externí odkaz:
https://doaj.org/article/18108820e24f456597c71e668ebe6ee9
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 44, Iss 7, Pp 606-608 (2016)
Major aortopulmonary collateral arteries are abnormal vascular structures that may be seen in cyanotic diseases that progress with reduced pulmonary flow. They occur rather rarely in the absence of cyanotic congenital heart disease. Presently describ
Externí odkaz:
https://doaj.org/article/58d9a63580444c47ba112d540369a1a5
Publikováno v:
Türk Kardiyoloji Derneği Arşivi, Vol 42, Iss 8, Pp 767-770 (2014)
Costello syndrome is a rare syndrome characterized by failure to thrive, short stature, mental motor retardation, characteristic facial features, macrocephaly, a short neck, loose soft skin with deep palmar and plantar creases, and hypertrichosis. Ca
Externí odkaz:
https://doaj.org/article/ddde9568d1784255bcb51dc0ab5f3412
Publikováno v:
Genel Tıp Dergisi, Vol 24, Iss 1, Pp 22-27 (2014)
Amaç: Bu çalışmada, çocuk kardiyoloji kliniğimizde üç yıl boyunca pulmoner balon valvüloplasti işlemi yapılan çocuklarla ilgili klinik deneyimlerimizin paylaşılması ve sonuçlarının değerlendirilmesi amaçlandı . Gereç ve yöntem
Externí odkaz:
https://doaj.org/article/4559e2b96115488288420fa3bc502900
Publikováno v:
Genel Tıp Dergisi, Vol 23, Iss 1, Pp 6-9 (2013)
Amaç: Bu retrospektrif çalışma nöral tüp defekti olan çocuklardaki doğuştan kalp hastalığı sıklığını belirlemek için yapılmıştır. Yöntem: Bu çalışmada, Selçuk Üniversitesi Tıp Fakültesi Etik Kurulu’ndan onay alındıkt
Externí odkaz:
https://doaj.org/article/dbe31bdf27a6445b97db938c0d6f45fb
Publikováno v:
Genel Tıp Dergisi, Vol 24, Iss 3, Pp 90-92 (2014)
Amaç: Kliniğimizde iki yıl boyunca transkateter yolla atriyal septal defekt kapatılması işlemi yapılan hastalarla ilgili klinik deneyimlerimizin paylaşılması ve sonuçlarının değerlendirilmesi amaçlandı. Gereç ve yöntemler: Çalışm
Externí odkaz:
https://doaj.org/article/b227c05a751244b098fad13053be1563
Publikováno v:
The Journal of Tepecik Education and Research Hospital. 33:142-145
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58be60339f61b88b7b1b5de1c6b4fc34
https://doi.org/10.4274/terh.galenos.2021.93653
https://doi.org/10.4274/terh.galenos.2021.93653