pubmed-article:18436217 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:18436217 | lifeskim:mentions | umls-concept:C0040223 | lld:lifeskim |
pubmed-article:18436217 | lifeskim:mentions | umls-concept:C0060520 | lld:lifeskim |
pubmed-article:18436217 | lifeskim:mentions | umls-concept:C0220825 | lld:lifeskim |
pubmed-article:18436217 | lifeskim:mentions | umls-concept:C0348016 | lld:lifeskim |
pubmed-article:18436217 | lifeskim:mentions | umls-concept:C0806487 | lld:lifeskim |
pubmed-article:18436217 | lifeskim:mentions | umls-concept:C1979874 | lld:lifeskim |
pubmed-article:18436217 | lifeskim:mentions | umls-concept:C0185125 | lld:lifeskim |
pubmed-article:18436217 | lifeskim:mentions | umls-concept:C0242842 | lld:lifeskim |
pubmed-article:18436217 | lifeskim:mentions | umls-concept:C0242841 | lld:lifeskim |
pubmed-article:18436217 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:18436217 | pubmed:dateCreated | 2008-7-28 | lld:pubmed |
pubmed-article:18436217 | pubmed:abstractText | Confocal laser scanning microscopy (CLSM) is reported to be a promising tool for in vivo histopathology during an endoscopy. The most commonly used fluorophore is fluorescein sodium given intravenously. However, so far, there are no objective data on contrast dynamics and image quality over time after injection of the substance. | lld:pubmed |
pubmed-article:18436217 | pubmed:language | eng | lld:pubmed |
pubmed-article:18436217 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18436217 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:18436217 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:18436217 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:18436217 | pubmed:month | Aug | lld:pubmed |
pubmed-article:18436217 | pubmed:issn | 1097-6779 | lld:pubmed |
pubmed-article:18436217 | pubmed:author | pubmed-author:SchmidRoland... | lld:pubmed |
pubmed-article:18436217 | pubmed:author | pubmed-author:MeiningAlexan... | lld:pubmed |
pubmed-article:18436217 | pubmed:author | pubmed-author:BeckerValenti... | lld:pubmed |
pubmed-article:18436217 | pubmed:author | pubmed-author:von... | lld:pubmed |
pubmed-article:18436217 | pubmed:author | pubmed-author:BajboujMonthe... | lld:pubmed |
pubmed-article:18436217 | pubmed:author | pubmed-author:KaragianniArt... | lld:pubmed |
pubmed-article:18436217 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:18436217 | pubmed:volume | 68 | lld:pubmed |
pubmed-article:18436217 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:18436217 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:18436217 | pubmed:pagination | 319-23 | lld:pubmed |
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pubmed-article:18436217 | pubmed:meshHeading | pubmed-meshheading:18436217... | lld:pubmed |
pubmed-article:18436217 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:18436217 | pubmed:articleTitle | Intravenous application of fluorescein for confocal laser scanning microscopy: evaluation of contrast dynamics and image quality with increasing injection-to-imaging time. | lld:pubmed |
pubmed-article:18436217 | pubmed:affiliation | II. Medical Department Internal Medicine, Klinikum Rechts der Isar, Technical University of Munich, Germany. | lld:pubmed |
pubmed-article:18436217 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:18436217 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:18436217 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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