| pubmed-article:17868863 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17868863 | lifeskim:mentions | umls-concept:C0014457 | lld:lifeskim |
| pubmed-article:17868863 | lifeskim:mentions | umls-concept:C0011906 | lld:lifeskim |
| pubmed-article:17868863 | lifeskim:mentions | umls-concept:C0220825 | lld:lifeskim |
| pubmed-article:17868863 | lifeskim:mentions | umls-concept:C0205322 | lld:lifeskim |
| pubmed-article:17868863 | lifeskim:mentions | umls-concept:C1706089 | lld:lifeskim |
| pubmed-article:17868863 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:17868863 | pubmed:dateCreated | 2007-9-17 | lld:pubmed |
| pubmed-article:17868863 | pubmed:abstractText | Hypereosinophilic syndromes (HES) are a group of heterogeneous disorders many of which remain ill-defined. By definition, the HES must be distinguished from other disorders with persistently elevated eosinophilia with a defined cause. Although marked eosinophilia worldwide is most commonly caused by helminth (worm) infections, the diagnostic approach must include noninfectious (nonparasitic) causes of marked eosinophilia as well. | lld:pubmed |
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