| pubmed-article:20671982 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20671982 | lifeskim:mentions | umls-concept:C0027651 | lld:lifeskim |
| pubmed-article:20671982 | lifeskim:mentions | umls-concept:C0020538 | lld:lifeskim |
| pubmed-article:20671982 | lifeskim:mentions | umls-concept:C0011710 | lld:lifeskim |
| pubmed-article:20671982 | lifeskim:mentions | umls-concept:C0332325 | lld:lifeskim |
| pubmed-article:20671982 | lifeskim:mentions | umls-concept:C1524003 | lld:lifeskim |
| pubmed-article:20671982 | pubmed:dateCreated | 2010-7-30 | lld:pubmed |
| pubmed-article:20671982 | pubmed:abstractText | We describe a young woman with longstanding resistant hypertension. Evaluation for renal artery stenosis and primary aldosteronism was unrevealing. In this setting of a suppressed plasma aldosterone concentration (PAC) and a suppressed plasma renin activity (PRA), a differential diagnosis of a deoxycorticosterone (DOC) producing tumor was entertained. Biochemical and imaging studies confirmed this diagnosis. Rare and novel DOC producing tumors are an important cause of resistant hypertension. | lld:pubmed |
| pubmed-article:20671982 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:20671982 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20671982 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20671982 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20671982 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20671982 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20671982 | pubmed:language | eng | lld:pubmed |
| pubmed-article:20671982 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:20671982 | pubmed:status | PubMed-not-MEDLINE | lld:pubmed |
| pubmed-article:20671982 | pubmed:issn | 1687-9635 | lld:pubmed |
| pubmed-article:20671982 | pubmed:author | pubmed-author:MelendezJoseJ | lld:pubmed |
| pubmed-article:20671982 | pubmed:author | pubmed-author:GuptaSaurabhS | lld:pubmed |
| pubmed-article:20671982 | pubmed:author | pubmed-author:KhannaApurvA | lld:pubmed |
| pubmed-article:20671982 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20671982 | pubmed:volume | 2010 | lld:pubmed |
| pubmed-article:20671982 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20671982 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20671982 | pubmed:pagination | 372719 | lld:pubmed |
| pubmed-article:20671982 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:20671982 | pubmed:articleTitle | Deoxycorticosterone producing tumor as a cause of resistant hypertension. | lld:pubmed |
| pubmed-article:20671982 | pubmed:affiliation | University of Connecticut Health Center, Farmington, CT 06030, USA. | lld:pubmed |
| pubmed-article:20671982 | pubmed:publicationType | Journal Article | lld:pubmed |
