| pubmed-article:8135917 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8135917 | lifeskim:mentions | umls-concept:C0087111 | lld:lifeskim |
| pubmed-article:8135917 | lifeskim:mentions | umls-concept:C0442027 | lld:lifeskim |
| pubmed-article:8135917 | lifeskim:mentions | umls-concept:C0003280 | lld:lifeskim |
| pubmed-article:8135917 | lifeskim:mentions | umls-concept:C1274040 | lld:lifeskim |
| pubmed-article:8135917 | lifeskim:mentions | umls-concept:C0456603 | lld:lifeskim |
| pubmed-article:8135917 | lifeskim:mentions | umls-concept:C1280500 | lld:lifeskim |
| pubmed-article:8135917 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
| pubmed-article:8135917 | lifeskim:mentions | umls-concept:C0022877 | lld:lifeskim |
| pubmed-article:8135917 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:8135917 | pubmed:dateCreated | 1993-9-7 | lld:pubmed |
| pubmed-article:8135917 | pubmed:abstractText | Patients receiving long-term anticoagulant therapy may be subject to unnecessary risks of bleeding or thromboembolism because of variability in the commercial thromboplastins used to determine prothrombin time and consequent uncertainty about the actual intensity of anticoagulation. | lld:pubmed |
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| pubmed-article:8135917 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:8135917 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:8135917 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8135917 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:8135917 | pubmed:issn | 0028-4793 | lld:pubmed |
| pubmed-article:8135917 | pubmed:author | pubmed-author:LevineH JHJ | lld:pubmed |
| pubmed-article:8135917 | pubmed:author | pubmed-author:PaukerS GSG | lld:pubmed |
| pubmed-article:8135917 | pubmed:author | pubmed-author:EckmanM HMH | lld:pubmed |
| pubmed-article:8135917 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8135917 | pubmed:day | 2 | lld:pubmed |
| pubmed-article:8135917 | pubmed:volume | 329 | lld:pubmed |
| pubmed-article:8135917 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8135917 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8135917 | pubmed:pagination | 696-702 | lld:pubmed |
| pubmed-article:8135917 | pubmed:dateRevised | 2010-3-24 | lld:pubmed |
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| pubmed-article:8135917 | pubmed:meshHeading | pubmed-meshheading:8135917-... | lld:pubmed |
| pubmed-article:8135917 | pubmed:year | 1993 | lld:pubmed |
| pubmed-article:8135917 | pubmed:articleTitle | Effect of laboratory variation in the prothrombin-time ratio on the results of oral anticoagulant therapy. | lld:pubmed |
| pubmed-article:8135917 | pubmed:affiliation | Division of Clinical Decision Making, New England Medical Center, Boston, MA 02111. | lld:pubmed |
| pubmed-article:8135917 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8135917 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:8135917 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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