pubmed-article:19925547 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19925547 | lifeskim:mentions | umls-concept:C0457113 | lld:lifeskim |
pubmed-article:19925547 | lifeskim:mentions | umls-concept:C1704257 | lld:lifeskim |
pubmed-article:19925547 | lifeskim:mentions | umls-concept:C0205182 | lld:lifeskim |
pubmed-article:19925547 | lifeskim:mentions | umls-concept:C1704258 | lld:lifeskim |
pubmed-article:19925547 | lifeskim:mentions | umls-concept:C0449450 | lld:lifeskim |
pubmed-article:19925547 | lifeskim:mentions | umls-concept:C0522498 | lld:lifeskim |
pubmed-article:19925547 | pubmed:issue | 6 | lld:pubmed |
pubmed-article:19925547 | pubmed:dateCreated | 2009-11-20 | lld:pubmed |
pubmed-article:19925547 | pubmed:abstractText | Left atrial appendage aneurysm (LAAA) is a rare condition caused by congenital dysplasia of the atrial muscles. Patients usually present with atrial tachyarrhythmias as a result of ectopic foci of atrial rhythm generation or systemic thromboembolism. We report a case of a 38-year-old Native American female presenting with 1-month history of cough, in sinus rhythm, and found to have a large cyst-like structure next to the left ventricular lateral wall on transthoracic echocardiography. This structure was later confirmed as a LAAA on cardiac magnetic resonance imaging. Patient underwent aneurysmectomy without any complications. | lld:pubmed |
pubmed-article:19925547 | pubmed:language | eng | lld:pubmed |
pubmed-article:19925547 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19925547 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:19925547 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19925547 | pubmed:issn | 1747-0803 | lld:pubmed |
pubmed-article:19925547 | pubmed:author | pubmed-author:SorrellVincen... | lld:pubmed |
pubmed-article:19925547 | pubmed:author | pubmed-author:BrodyEric AEA | lld:pubmed |
pubmed-article:19925547 | pubmed:author | pubmed-author:KalraNishantN | lld:pubmed |
pubmed-article:19925547 | pubmed:author | pubmed-author:WilsonDenaD | lld:pubmed |
pubmed-article:19925547 | pubmed:author | pubmed-author:Van DykHenryH | lld:pubmed |
pubmed-article:19925547 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:19925547 | pubmed:volume | 4 | lld:pubmed |
pubmed-article:19925547 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19925547 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19925547 | pubmed:pagination | 489-93 | lld:pubmed |
pubmed-article:19925547 | pubmed:dateRevised | 2011-5-5 | lld:pubmed |
pubmed-article:19925547 | pubmed:meshHeading | pubmed-meshheading:19925547... | lld:pubmed |
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pubmed-article:19925547 | pubmed:meshHeading | pubmed-meshheading:19925547... | lld:pubmed |
pubmed-article:19925547 | pubmed:meshHeading | pubmed-meshheading:19925547... | lld:pubmed |
pubmed-article:19925547 | pubmed:articleTitle | Left atrial appendage aneurysm-a rare anomaly with an atypical presentation. | lld:pubmed |
pubmed-article:19925547 | pubmed:affiliation | Department of Internal Medicine, Division of Cardiology, University of Arizona, Tucson, AZ 85724, USA. | lld:pubmed |
pubmed-article:19925547 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19925547 | pubmed:publicationType | Case Reports | lld:pubmed |