pubmed-article:1647470 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:1647470 | lifeskim:mentions | umls-concept:C0003662 | lld:lifeskim |
pubmed-article:1647470 | lifeskim:mentions | umls-concept:C0151729 | lld:lifeskim |
pubmed-article:1647470 | lifeskim:mentions | umls-concept:C0020852 | lld:lifeskim |
pubmed-article:1647470 | lifeskim:mentions | umls-concept:C0444626 | lld:lifeskim |
pubmed-article:1647470 | lifeskim:mentions | umls-concept:C0085973 | lld:lifeskim |
pubmed-article:1647470 | lifeskim:mentions | umls-concept:C0007320 | lld:lifeskim |
pubmed-article:1647470 | pubmed:issue | 3 | lld:pubmed |
pubmed-article:1647470 | pubmed:dateCreated | 1991-7-31 | lld:pubmed |
pubmed-article:1647470 | pubmed:abstractText | We report on a 35 year old patient suffering from heterochromia complicata Fuchs with a mature cataract. Multiple small whitish-yellowish crystal-lines on the iris at the 7 and 12 o'clock position were interpreted as Russell bodies and correlated with an elevated concentration of 7.2 mg/dl IgG in the aqueous humor analysis. IgA und IgM could not be detected (less than 1.1 mg/dl). Three months after an unremarkable extracapsular cataract extraction and posterior chamber lens implantation a positive Tyndall phenomenon and Russell bodies were found at just the same locations on the iris. | lld:pubmed |
pubmed-article:1647470 | pubmed:language | ger | lld:pubmed |
pubmed-article:1647470 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1647470 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:1647470 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:1647470 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:1647470 | pubmed:month | Mar | lld:pubmed |
pubmed-article:1647470 | pubmed:issn | 0023-2165 | lld:pubmed |
pubmed-article:1647470 | pubmed:author | pubmed-author:NaumannG OGO | lld:pubmed |
pubmed-article:1647470 | pubmed:author | pubmed-author:GierthKK | lld:pubmed |
pubmed-article:1647470 | pubmed:author | pubmed-author:BialasiewiczA... | lld:pubmed |
pubmed-article:1647470 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:1647470 | pubmed:volume | 198 | lld:pubmed |
pubmed-article:1647470 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:1647470 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:1647470 | pubmed:pagination | 205-6 | lld:pubmed |
pubmed-article:1647470 | pubmed:dateRevised | 2009-11-11 | lld:pubmed |
pubmed-article:1647470 | pubmed:meshHeading | pubmed-meshheading:1647470-... | lld:pubmed |
pubmed-article:1647470 | pubmed:meshHeading | pubmed-meshheading:1647470-... | lld:pubmed |
pubmed-article:1647470 | pubmed:meshHeading | pubmed-meshheading:1647470-... | lld:pubmed |
pubmed-article:1647470 | pubmed:meshHeading | pubmed-meshheading:1647470-... | lld:pubmed |
pubmed-article:1647470 | pubmed:meshHeading | pubmed-meshheading:1647470-... | lld:pubmed |
pubmed-article:1647470 | pubmed:meshHeading | pubmed-meshheading:1647470-... | lld:pubmed |
pubmed-article:1647470 | pubmed:meshHeading | pubmed-meshheading:1647470-... | lld:pubmed |
pubmed-article:1647470 | pubmed:meshHeading | pubmed-meshheading:1647470-... | lld:pubmed |
pubmed-article:1647470 | pubmed:meshHeading | pubmed-meshheading:1647470-... | lld:pubmed |
pubmed-article:1647470 | pubmed:meshHeading | pubmed-meshheading:1647470-... | lld:pubmed |
pubmed-article:1647470 | pubmed:year | 1991 | lld:pubmed |
pubmed-article:1647470 | pubmed:articleTitle | [Heterochromia complicata Fuchs, crystalline iridopathy and increased immunoglobulin G in aqueous humor. A case report]. | lld:pubmed |
pubmed-article:1647470 | pubmed:affiliation | Augenklinik mit Poliklinik, Universität Erlangen-Nürnberg. | lld:pubmed |
pubmed-article:1647470 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:1647470 | pubmed:publicationType | English Abstract | lld:pubmed |
pubmed-article:1647470 | pubmed:publicationType | Case Reports | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:1647470 | lld:pubmed |