pubmed-article:15316209 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:15316209 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:15316209 | lifeskim:mentions | umls-concept:C0016832 | lld:lifeskim |
pubmed-article:15316209 | lifeskim:mentions | umls-concept:C0031521 | lld:lifeskim |
pubmed-article:15316209 | lifeskim:mentions | umls-concept:C0010674 | lld:lifeskim |
pubmed-article:15316209 | lifeskim:mentions | umls-concept:C0683278 | lld:lifeskim |
pubmed-article:15316209 | lifeskim:mentions | umls-concept:C0204727 | lld:lifeskim |
pubmed-article:15316209 | lifeskim:mentions | umls-concept:C0205409 | lld:lifeskim |
pubmed-article:15316209 | lifeskim:mentions | umls-concept:C0033522 | lld:lifeskim |
pubmed-article:15316209 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:15316209 | pubmed:dateCreated | 2004-8-18 | lld:pubmed |
pubmed-article:15316209 | pubmed:abstractText | Patients with cystic fibrosis (CF) are at an increased risk of pulmonary colonisation by opportunistic micro-organisms. Using specialised methods, the black yeast Exophiala dermatitidis could consistently be cultured from CF patients. Isolation rates from sputum samples ranged between 1.8 and 15.7%. Occasionally, infection could be recognised. | lld:pubmed |
pubmed-article:15316209 | pubmed:language | eng | lld:pubmed |
pubmed-article:15316209 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:15316209 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:15316209 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:15316209 | pubmed:issn | 0025-7931 | lld:pubmed |
pubmed-article:15316209 | pubmed:author | pubmed-author:SchaalK PKP | lld:pubmed |
pubmed-article:15316209 | pubmed:author | pubmed-author:de HoogG SGS | lld:pubmed |
pubmed-article:15316209 | pubmed:author | pubmed-author:SiekmeierRR | lld:pubmed |
pubmed-article:15316209 | pubmed:author | pubmed-author:SchnitzlerNN | lld:pubmed |
pubmed-article:15316209 | pubmed:author | pubmed-author:SterzikBB | lld:pubmed |
pubmed-article:15316209 | pubmed:author | pubmed-author:HorréRR | lld:pubmed |
pubmed-article:15316209 | pubmed:copyrightInfo | Copyright 2004 S. Karger AG, Basel | lld:pubmed |
pubmed-article:15316209 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:15316209 | pubmed:volume | 71 | lld:pubmed |
pubmed-article:15316209 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:15316209 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:15316209 | pubmed:pagination | 360-6 | lld:pubmed |
pubmed-article:15316209 | pubmed:dateRevised | 2009-11-11 | lld:pubmed |
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pubmed-article:15316209 | pubmed:articleTitle | Isolation of fungi, especially Exophiala dermatitidis, in patients suffering from cystic fibrosis. A prospective study. | lld:pubmed |
pubmed-article:15316209 | pubmed:affiliation | Institute for Medical Microbiology and Immunology, University of Bonn, Bonn, The Netherlands. horre@bfarm.de | lld:pubmed |
pubmed-article:15316209 | pubmed:publicationType | Journal Article | lld:pubmed |
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