34 results on '"Tormene D"'
Search Results
2. Systemic Catheter-Related Venous Thromboembolism in Children: Data From the Italian Registry of Pediatric Thrombosis
3. The incidence of VTE in asymptomatic carriers of a deficiency of at, PC OR PS: a prospective cohort study
4. High vs. low doses of low‐molecular‐weight heparin for the treatment of superficial vein thrombosis of the legs: a double‐blind, randomized trial
5. Aspirin for preventing the recurrence of venous thromboembolism
6. Risk for subsequent venous thromboembolic complications in carriers of the prothrombin or the factor V gene mutation with a first episode of deep-vein thrombosis
7. Circulating microparticles in carriers of factor V Leiden mutation
8. Factor IX activity/antigen ratio and the risk of unprovoked venous thrombosis
9. Erratum to Similar hypercoagulable state and thrombosis risk in type I and type III protein S-deficient individuals from mixed type I/III
10. Screening for thrombophilia and antithromboticprophylaxis in pregnancy: Guidelines of the Italian Society for Haemostasis andThrombosis (SISET)
11. Type III protein S deficiency is associated with a hypercoagulable state and an increased risk of venous thrombosis
12. Thrombophilia does not increase the risk of the post-thrombotic syndrome. A prospective cohort study
13. Objectives and methodology: Guidelines of the ItalianSociety for Haemostasis and Thrombosis (SISET)
14. Thrombin generation in carriers of inheroted clotting inhibitors defects
15. Platelet protein S antigen levels in congenital protein S deficiency
16. Evidence of the first X-linked thrombophilia due to a novel mutation in clotting factor IX gene resulting in hyperfunctional fix: factor IX arginine 338 leucine (factor IX padua)
17. Thrombosis in children
18. Increased endogenous thrombin potential (ETP) in carriers of inherited clotting inhibitors defects
19. Increased Endogenous Thrombin Potential (ETP) in patients of families with inherited AT defects
20. Thrombophilia as a predictor of residual vein thrombosis. A prospective cohort study
21. Screening for venous thrombophilia: pros
22. Thrombophilia and thrombosis in adults and children
23. The PAI-1 gene 4G/5G polymorphism and deep vein thrombosis in patients with inherited thrombophilia
24. Venous thromboembolism, fetal loss and preeclampsia in pregnant women with congenital thrombophilia
25. 4G/5G polymorphism of PAI-1 gene promoter: an additional possible prothrombotic factor in congenital thrombophilia
26. Combination of 4 mutations (FV R506Q, FV H1299R,Fv Y1702C, PT 20210)affecting the prothrombinase complex in a thrombophilic family
27. The incidence of venous thromboembolism in asymptomatic carriers of a deficiency of antithrombin, protein C, or protein S: a prospective cohort study
28. APC resistance, oral contraceptive therapy and deep vein thrombosis: Settled and unsettled problems
29. Hyperhomosysteinemia and deep-vein thrombosis. A case-control study
30. Factor V Leiden mutation and the risk of venous thromboembolism in pregnant women
31. The risk of recurrent venous thromboembolism in patients with inherited deficiency of natural anticoagulants antithrombin, protein C and protein S
32. Combined heterozygous plasminogen deficiency and factor V Leiden defect in the same kindred
33. Factor V Leiden and prothrombin gene mutation in inflammatory bowel disease in a Mediterranean area
34. Objectives and methodology: Guidelines of the Italian Society for Haemostasis and Thrombosis (SISET)
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