| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 9185522 | Thrombosis Research | 2005 | 13 Pages | 
Abstract
												Estrogen, tamoxifen and raloxifene affected hemostasis favoring procoagulation and impairing anticoagulation. The biochemical effects of the selective estrogen receptor modulators (SERMs) were distinct from those of estrogen and differed only subtly from each other.
											Keywords
												FXIFVIIFVIIIAPTTCEEvWFFIITAFIPAI-1APCSERMsPulmonary embolismhERsantithrombinWomen's Health InitiativeEstradiolEstrogenConjugated equine estrogenEstrogen TherapytamoxifenVenous thrombosisDeep vein thrombosisDVTFIXRelative riskRaloxifeneactivated partial thromboplastin timebody mass indexBMIVon Willebrand factorFactor VIIIFactor IXFactor VIIFactor XISelective estrogen receptor modulatorsHeart and Estrogen/Progestin Replacement StudyPlasminogen activator inhibitor-1Thrombin activatable fibrinolysis inhibitorHormone therapyHemostasiswhiActivated protein C
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											Authors
												F. Cosman, M. Baz-Hecht, M. Cushman, M.D. Vardy, J.D. Cruz, J.W. Nieves, M. Zion, R. Lindsay, 
											