pubmed-article:19828585 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19828585 | lifeskim:mentions | umls-concept:C1801960 | lld:lifeskim |
pubmed-article:19828585 | lifeskim:mentions | umls-concept:C0003496 | lld:lifeskim |
pubmed-article:19828585 | lifeskim:mentions | umls-concept:C2699153 | lld:lifeskim |
pubmed-article:19828585 | lifeskim:mentions | umls-concept:C1269955 | lld:lifeskim |
pubmed-article:19828585 | lifeskim:mentions | umls-concept:C0677535 | lld:lifeskim |
pubmed-article:19828585 | pubmed:issue | 1 | lld:pubmed |
pubmed-article:19828585 | pubmed:dateCreated | 2010-1-21 | lld:pubmed |
pubmed-article:19828585 | pubmed:abstractText | Neurofibromatosis type 1 (NF-1) is an autosomal dominant disease primarily characterized by cutaneous café au lait macules, benign neurofibromas, and iris hamartomas. A spectrum of vascular abnormalities is associated with NF-1. We present a case of a 49-year-old female with NF-1 and spontaneous rupture of the infrarenal aorta caused by invasion of a neurofibroma and treated with endovascular stent grafting. | lld:pubmed |
pubmed-article:19828585 | pubmed:language | eng | lld:pubmed |
pubmed-article:19828585 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:19828585 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:19828585 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19828585 | pubmed:month | Jan | lld:pubmed |
pubmed-article:19828585 | pubmed:issn | 1938-9116 | lld:pubmed |
pubmed-article:19828585 | pubmed:author | pubmed-author:MakarounMiche... | lld:pubmed |
pubmed-article:19828585 | pubmed:author | pubmed-author:GoMichael RMR | lld:pubmed |
pubmed-article:19828585 | pubmed:author | pubmed-author:ChaerRabih... | lld:pubmed |
pubmed-article:19828585 | pubmed:author | pubmed-author:BarilDonald... | lld:pubmed |
pubmed-article:19828585 | pubmed:author | pubmed-author:OakleyGerard... | lld:pubmed |
pubmed-article:19828585 | pubmed:author | pubmed-author:FalconeJohn... | lld:pubmed |
pubmed-article:19828585 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:19828585 | pubmed:volume | 44 | lld:pubmed |
pubmed-article:19828585 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19828585 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19828585 | pubmed:pagination | 52-5 | lld:pubmed |
pubmed-article:19828585 | pubmed:meshHeading | pubmed-meshheading:19828585... | lld:pubmed |
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pubmed-article:19828585 | pubmed:meshHeading | pubmed-meshheading:19828585... | lld:pubmed |
pubmed-article:19828585 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:19828585 | pubmed:articleTitle | Vascular wall invasion in neurofibromatosis-induced aortic rupture. | lld:pubmed |
pubmed-article:19828585 | pubmed:affiliation | Division of Vascular Surgery, Department of Pathology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania 15213, USA. | lld:pubmed |
pubmed-article:19828585 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19828585 | pubmed:publicationType | Case Reports | lld:pubmed |