| pubmed-article:15113383 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:15113383 | lifeskim:mentions | umls-concept:C0005795 | lld:lifeskim |
| pubmed-article:15113383 | lifeskim:mentions | umls-concept:C0042974 | lld:lifeskim |
| pubmed-article:15113383 | lifeskim:mentions | umls-concept:C0011900 | lld:lifeskim |
| pubmed-article:15113383 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:15113383 | pubmed:dateCreated | 2004-4-28 | lld:pubmed |
| pubmed-article:15113383 | pubmed:abstractText | We report the case of a long-standing female blood donor whose blood donation was processed for cryoprecipitate. The cryoprecipitate unit was chosen at random for FVIII:C estimation as part of the quality control, and a low FVIII:C level was identified. The cause of this was subsequently shown to be the Normandy variant of type-2 von Willebrand's disease due to a homozygous Arg854Gln mutation in the von Willebrand factor gene. | lld:pubmed |
| pubmed-article:15113383 | pubmed:language | eng | lld:pubmed |
| pubmed-article:15113383 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15113383 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:15113383 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15113383 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15113383 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:15113383 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:15113383 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:15113383 | pubmed:issn | 0958-7578 | lld:pubmed |
| pubmed-article:15113383 | pubmed:author | pubmed-author:MakrisMM | lld:pubmed |
| pubmed-article:15113383 | pubmed:author | pubmed-author:KashyapSS | lld:pubmed |
| pubmed-article:15113383 | pubmed:author | pubmed-author:NesbittI MIM | lld:pubmed |
| pubmed-article:15113383 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:15113383 | pubmed:volume | 14 | lld:pubmed |
| pubmed-article:15113383 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:15113383 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:15113383 | pubmed:pagination | 181-4 | lld:pubmed |
| pubmed-article:15113383 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
| pubmed-article:15113383 | pubmed:meshHeading | pubmed-meshheading:15113383... | lld:pubmed |
| pubmed-article:15113383 | pubmed:meshHeading | pubmed-meshheading:15113383... | lld:pubmed |
| pubmed-article:15113383 | pubmed:meshHeading | pubmed-meshheading:15113383... | lld:pubmed |
| pubmed-article:15113383 | pubmed:meshHeading | pubmed-meshheading:15113383... | lld:pubmed |
| pubmed-article:15113383 | pubmed:meshHeading | pubmed-meshheading:15113383... | lld:pubmed |
| pubmed-article:15113383 | pubmed:meshHeading | pubmed-meshheading:15113383... | lld:pubmed |
| pubmed-article:15113383 | pubmed:meshHeading | pubmed-meshheading:15113383... | lld:pubmed |
| pubmed-article:15113383 | pubmed:meshHeading | pubmed-meshheading:15113383... | lld:pubmed |
| pubmed-article:15113383 | pubmed:meshHeading | pubmed-meshheading:15113383... | lld:pubmed |
| pubmed-article:15113383 | pubmed:meshHeading | pubmed-meshheading:15113383... | lld:pubmed |
| pubmed-article:15113383 | pubmed:meshHeading | pubmed-meshheading:15113383... | lld:pubmed |
| pubmed-article:15113383 | pubmed:meshHeading | pubmed-meshheading:15113383... | lld:pubmed |
| pubmed-article:15113383 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:15113383 | pubmed:articleTitle | Unconventional diagnosis of Normandy-type von Willebrand's disease in a blood donor. | lld:pubmed |
| pubmed-article:15113383 | pubmed:affiliation | Sheffield Haemophilia and Thrombosis Centre, Royal Hallamshire Hospital, Glossop Road, Sheffield S10 2JF, UK. | lld:pubmed |
| pubmed-article:15113383 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:15113383 | pubmed:publicationType | Case Reports | lld:pubmed |
