| pubmed-article:14707415 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:14707415 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:14707415 | lifeskim:mentions | umls-concept:C0151945 | lld:lifeskim |
| pubmed-article:14707415 | lifeskim:mentions | umls-concept:C0598608 | lld:lifeskim |
| pubmed-article:14707415 | lifeskim:mentions | umls-concept:C0852077 | lld:lifeskim |
| pubmed-article:14707415 | lifeskim:mentions | umls-concept:C1260403 | lld:lifeskim |
| pubmed-article:14707415 | lifeskim:mentions | umls-concept:C0380964 | lld:lifeskim |
| pubmed-article:14707415 | lifeskim:mentions | umls-concept:C0332240 | lld:lifeskim |
| pubmed-article:14707415 | pubmed:issue | 2-3 | lld:pubmed |
| pubmed-article:14707415 | pubmed:dateCreated | 2004-3-22 | lld:pubmed |
| pubmed-article:14707415 | pubmed:abstractText | Idiopathic cerebral vein thrombosis (iCVT) represents approximately 30% of the cases of cerebral vein thrombosis (CVT). New, inherited - factor V Leiden (FVL) and prothrombin gene mutation (PTHRA20210) - and inherited/acquired - hyperhomocysteinemia (HHcy) - prothrombotic conditions have been detected recently. | lld:pubmed |
| pubmed-article:14707415 | pubmed:language | eng | lld:pubmed |
| pubmed-article:14707415 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:14707415 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:14707415 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:14707415 | pubmed:issn | 1015-9770 | lld:pubmed |
| pubmed-article:14707415 | pubmed:author | pubmed-author:SalvioliGianf... | lld:pubmed |
| pubmed-article:14707415 | pubmed:author | pubmed-author:MariettaMarco... | lld:pubmed |
| pubmed-article:14707415 | pubmed:author | pubmed-author:VenturaPaoloP | lld:pubmed |
| pubmed-article:14707415 | pubmed:author | pubmed-author:PaniniRossana... | lld:pubmed |
| pubmed-article:14707415 | pubmed:author | pubmed-author:RosaMaria... | lld:pubmed |
| pubmed-article:14707415 | pubmed:author | pubmed-author:CobelliMilena... | lld:pubmed |
| pubmed-article:14707415 | pubmed:copyrightInfo | Copyright 2004 S. Karger AG, Basel | lld:pubmed |
| pubmed-article:14707415 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:14707415 | pubmed:volume | 17 | lld:pubmed |
| pubmed-article:14707415 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:14707415 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:14707415 | pubmed:pagination | 153-9 | lld:pubmed |
| pubmed-article:14707415 | pubmed:dateRevised | 2004-11-17 | lld:pubmed |
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| pubmed-article:14707415 | pubmed:year | 2004 | lld:pubmed |
| pubmed-article:14707415 | pubmed:articleTitle | Hyperhomocysteinemia and other newly recognized inherited coagulation disorders (factor V Leiden and prothrombin gene mutation) in patients with idiopathic cerebral vein thrombosis. | lld:pubmed |
| pubmed-article:14707415 | pubmed:affiliation | Department of Internal Medicine, University of Modena and Reggio Emilia, Italy. paoloven@unimore.it | lld:pubmed |
| pubmed-article:14707415 | pubmed:publicationType | Journal Article | lld:pubmed |
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