Examples of using Vwf in English and their translations into Polish
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IU*** human von Willebrand factor** VWF.
VWF and FVIII are involved in blood clotting.
Furthermore patients may develop inhibitors to FVIII and VWF.
A lack of vWF impairs platelet stickiness and clumping.
Hereditary vWD is caused by mutations that impair vWF synthesis, release, or stability.
VWF produces delayed correction of the associated FVIII deficiency.
The ratio between FVIII:C and VWF: RCo in a vial is approximately 1:2.4.
The vWF gene is located on the short arm p of chromosome 12 12p13.2.
If you have VWD your doctor will prescribe you Voncento with the number of units of VWF specified.
The amount of VWF and FVIII you need to take and the duration of treatment depend on.
Exogenously administered human plasma-derived VWF behaves in the same way as endogenous VWF.
In addition, vWF is a carrier protein for coagulation Factor VIII necessary for blood to clot.
Transfusion of fresh whole blood, fresh plasma, fresh frozen plasma, andcryoprecipitate will supply vWF to the blood.
Generally, 1 IU/kg VWF: RCo raises the circulating level of VWF: RCo by 0.02 IU/ml 2.
Results from studies in pigs showed that the application of von Willebrand Factor(vWF, 66 I.U./kg body weight) markedly reduced the bleeding time.
The FVIII/VWF complex consists of two molecules(FVIII and VWF) with different physiological functions.
As Voncento contains both FVIII and VWF, it is important to know which factor you most need.
VWF is an autosomal trait, which both males and females express and transmit genetically and with equal frequency.
Administration of a FVIII:C containing VWF preparation restores the FVIII: C level to normal immediately after the first infusion.
VWF inhibition: Patients with VWD, especially type 3 patients, may develop neutralising antibodies(inhibitors) to VWF.
A clinical diagnosis of von Willebrand disease is based on a specific measurement of plasma vWF concentration bound to the antigen vWF: Ag.
If a dog lacking vWF requires surgery, a pre-operative transfusion should be given just before the procedure.
The product is made from human plasma(the liquid part of the blood) and contains the active substances called human coagulation factor VIII(FVIII) andhuman von Willebrand factor VWF.
Voncento contains FVIII and VWF as active ingredients which are derived from human plasma and act like endogenous constituents of plasma.
Endothelin- a peptide produced by endothelium, a potent spasmogen, a proliferative factor of smooth muscles andthe von Willebrand factor(vWF) are included among markers of endothelial damage.
The factor VIII/von Willebrand factor(vWF) complex consists of two molecules(factor VIII and vWF) with different physiological functions.
The BMBT test,along with the platelet function analyzer(PFA 100), are point-of-care screening tests where the endpoints are prolonged in patients with platelet clumping defects and vWF deficiency.
Administered intravenously, VWF binds to endogenous FVIII(which is produced normally by the patient), and by stabilising this factor, avoids its rapid degradation.
Von Willebrand's disease(vWD)is a blood disease caused by a deficiency of von Willebrand Factor(vWF), an adhesive glycoprotein in the blood required for normal platelet binding(i.e., clotting) at the sites of small blood vessel injuries.
Administration of VWF allows correction of the haemostatic abnormalities exhibited by patients who suffer from VWF deficiency(VWD) at two levels.