pubmed-article:8418289 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:8418289 | lifeskim:mentions | umls-concept:C0010674 | lld:lifeskim |
pubmed-article:8418289 | lifeskim:mentions | umls-concept:C0033809 | lld:lifeskim |
pubmed-article:8418289 | lifeskim:mentions | umls-concept:C2709248 | lld:lifeskim |
pubmed-article:8418289 | lifeskim:mentions | umls-concept:C0206173 | lld:lifeskim |
pubmed-article:8418289 | lifeskim:mentions | umls-concept:C0205191 | lld:lifeskim |
pubmed-article:8418289 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:8418289 | pubmed:dateCreated | 1993-1-29 | lld:pubmed |
pubmed-article:8418289 | pubmed:abstractText | The epidemiology of pulmonary colonisation by Pseudomonas aeruginosa was studied in 21 patients with cystic fibrosis (CF) by field inversion gel electrophoresis. DraI-DNA restriction patterns were analysed for 187 P. aeruginosa isolates from these patients. The results revealed that the strains present in individual patients varied during the course of chronic colonisation; the emergence of new strains often was associated with periods of antibiotic therapy. Patients often were colonised by more than one strain (two or three strains were present in 54% of the patients) and the strains obtained from unrelated patients were highly heterogeneous, in contrast to those isolated from a pair of twins. These results demonstrate the heterogeneity and variability of P. aeruginosa isolates in the pulmonary flora of chronically infected CF patients. | lld:pubmed |
pubmed-article:8418289 | pubmed:language | eng | lld:pubmed |
pubmed-article:8418289 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8418289 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:8418289 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:8418289 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:8418289 | pubmed:month | Jan | lld:pubmed |
pubmed-article:8418289 | pubmed:issn | 0022-2615 | lld:pubmed |
pubmed-article:8418289 | pubmed:author | pubmed-author:LenoirGG | lld:pubmed |
pubmed-article:8418289 | pubmed:author | pubmed-author:VéronMM | lld:pubmed |
pubmed-article:8418289 | pubmed:author | pubmed-author:BerchePP | lld:pubmed |
pubmed-article:8418289 | pubmed:author | pubmed-author:ScheinmannPP | lld:pubmed |
pubmed-article:8418289 | pubmed:author | pubmed-author:BoukadidaJJ | lld:pubmed |
pubmed-article:8418289 | pubmed:author | pubmed-author:De... | lld:pubmed |
pubmed-article:8418289 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:8418289 | pubmed:volume | 38 | lld:pubmed |
pubmed-article:8418289 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:8418289 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:8418289 | pubmed:pagination | 29-33 | lld:pubmed |
pubmed-article:8418289 | pubmed:dateRevised | 2008-8-28 | lld:pubmed |
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pubmed-article:8418289 | pubmed:year | 1993 | lld:pubmed |
pubmed-article:8418289 | pubmed:articleTitle | Molecular epidemiology of chronic pulmonary colonisation by Pseudomonas aeruginosa in cystic fibrosis. | lld:pubmed |
pubmed-article:8418289 | pubmed:affiliation | Laboratoire de Microbiologie, Hôpital Necker-Enfants Malades, Paris, France. | lld:pubmed |
pubmed-article:8418289 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:8418289 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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