Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Congenital cardiovascular anomaly"'
Publikováno v:
Pakistan Armed Forces Medical Journal. 70:S912-15
Double Aortic Arch is a rare congenital cardiovascular anomaly. Its first successful surgery was performed by Robert Gross in 1945 at Children Hospital Boston, USA. It accounts for 0.4 to 1% of all congenital cardiac defects. Patients having a Double
Akademický článek
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Publikováno v:
Journal of Avian Medicine and Surgery, 2001 Jun 01. 15(2), 101-106.
Externí odkaz:
https://www.jstor.org/stable/30135622
Autor:
Pouya Youssefi, Mustafa Zakkar, Christophe Acar, Emmanuel Lansac, Nizar Khelil, Mathieu Debauchez
Publikováno v:
Annals of Cardiothoracic Surgery. 8:401-410
The bicuspid aortic valve (BAV) is the most common congenital cardiovascular anomaly and may present with differing phenotypes including almost constant annular dilation. We have developed a standardized approach to BAV repair with a systematic adjun
Autor:
Rika Suda, Jun Ikari, Takayuki Jujo, Goro Matsumiya, Seiichiro Sakao, Kaoru Matsuura, Hajime Kasai, Takayuki Kobayashi, Akira Naito, Nobuhiro Tanabe, Kengo Shimazu, Rintaro Nishimura, Koichiro Tatsumi, Nozomi Tanaka, Toshihiko Sugiura
Publikováno v:
Respiratory Medicine Case Reports, Vol 25, Iss, Pp 112-115 (2018)
Respiratory Medicine Case Reports
Respiratory Medicine Case Reports
Partial anomalous pulmonary venous return (PAPVR) is a rare congenital cardiovascular anomaly. A 68-year-old woman was referred to our hospital for detailed examination for pulmonary hypertension (PH). She had been diagnosed as having pulmonary arter
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Publikováno v:
Surgical Management of Aortic Pathology ISBN: 9783709148723
Bicuspid aortic valve (BAV) disease is the most common congenital cardiovascular anomaly with the majority of patients requiring surgical intervention over the course of their lives. BAV aortopathy is increasingly recognized; however, the appropriate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bab665cc80e04c74c296de31cc2a6d60
https://doi.org/10.1007/978-3-7091-4874-7_35
https://doi.org/10.1007/978-3-7091-4874-7_35
Autor:
Kevin Fan-Ying Tseng
Publikováno v:
Case Reports in Surgery
Case Reports in Surgery, Vol 2013 (2013)
Case Reports in Surgery, Vol 2013 (2013)
Anomalous origin of the left coronary artery from the pulmonary trunk, also known as Garland-Bland-White syndrome, is an extremely rare but potentially fatal congenital cardiovascular anomaly, and it often exists as an isolated condition. We hereby r
Publikováno v:
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Background: Persistent left cranial vena cava with absent right cranial vena cava is a rare anomaly. Congenitally persistent left cranial vena cava is the most common variant of the systemic venous return to the heart, embryologically resulting from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::a4e68b547aaed10fcdd6bbf1335a956f