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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2011-1-4
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pubmed:abstractText |
Anomalous origin of one pulmonary artery branch from the aorta in the presence of separate aortic and pulmonary valves is a rare but important entity necessitating early diagnosis and surgery to prevent irreversible vascular pulmonary disease. We evaluated our experience with seven infants having this anomaly.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1016-5169
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
38
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
411-5
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pubmed:meshHeading |
pubmed-meshheading:21200120-Abnormalities, Multiple,
pubmed-meshheading:21200120-Aorta,
pubmed-meshheading:21200120-Ductus Arteriosus, Patent,
pubmed-meshheading:21200120-Female,
pubmed-meshheading:21200120-Foramen Ovale, Patent,
pubmed-meshheading:21200120-Humans,
pubmed-meshheading:21200120-Infant,
pubmed-meshheading:21200120-Infant, Newborn,
pubmed-meshheading:21200120-Male,
pubmed-meshheading:21200120-Postoperative Complications,
pubmed-meshheading:21200120-Pulmonary Artery
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pubmed:year |
2010
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pubmed:articleTitle |
Anomalous origin of one pulmonary artery branch from the ascending aorta: experience of our center.
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pubmed:affiliation |
Department of Pediatric Cardiology, Siyami Ersek Cardiovascular Surgery Center, ?stanbul, Turkey. drabdullaherdem@hotmail.com
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pubmed:publicationType |
Journal Article
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