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ThrombophiliaActivated protein c resistanceCoagulation factor viiHaemophilia bHaemophilia aProthrombin g20210aHaemophiliaFactor vCoagulopathyAntiphospholipid syndromeFactor viiiHemolytic anemiaHeparin-induced thrombocytopeniaProthrombin complex concentrateBleeding diathesisMicroangiopathic hemolytic anemiaThrombotic microangiopathyHemoglobinemiaPortal vein thrombosisHaemophilia cPlatelet plugThromboxane a2Recombinant factor viiaFibrinoid necrosisD-dimerThrombosisHemoglobinopathyMonoclonal gammopathyThrombinDirect factor xa inhibitorsProtease-activated receptor 2Renal vein thrombosisCerebral venous sinus thrombosisTissue factorHyperviscosity syndromeGiant platelet disorderPolycythemiaCerebral vasculitisMicroangiopathyPlasminogen activator inhibitor-1Essential thrombocythemiaPost-thrombotic syndromeFamilial hypercholesterolemiaFibromuscular dysplasiaThrombocythemiaFibrin degradation productHaematopoiesisHyperhomocysteinemiaPlateletFactor xiiiGranulomatosis with polyangiitisAutoimmune hemolytic anemiaHemoglobin variantsRed cell agglutinationCoronary artery diseaseAnagrelideApixabanCoronary thrombosisThrombin timeSuperior vena cava syndromeContact activation systemCold agglutinin diseaseThrombolysisPolychromasiaDeep vein thrombosisHemolytic jaundiceBlood typeNeutrophiliaThrombophlebitisHemoglobin cAnticoagulantPlatelet transfusionCryoglobulinemiaSystemic vasculitisIron overloadAlpha-5 beta-1Purpura fulminansCavernous sinus thrombosisLupus anticoagulantAdamts13Fas receptorHemoglobin constant springThrombopoietin receptorHemoglobinuriaPlasminMixing studyComplement component 5aCerebral amyloid angiopathyTrousseau sign of malignancyGpviEvans syndromeProtein s deficiencyPost-transfusion purpuraThromboangiitis obliteransHyperlipidemiaHemagglutinationHypercholesterolemiaFactor ixInterleukin 1 betaTraumatic aortic rupture