271 results on '"Tormene D"'
Search Results
2. The new Italian registry of infantile thrombosis (RITI): A reflection on its journey, challenges and pitfalls
3. Systemic Catheter-Related Venous Thromboembolism in Children: Data From the Italian Registry of Pediatric Thrombosis
4. Genetic modulation of the FVLeiden/normal FV ratio and risk of venous thrombosis in factor V Leiden heterozygotes
5. A risk assessment model for the identification of hospitalized medical patients at risk for venous thromboembolism: the Padua Prediction Score
6. Hereditary and acquired protein S deficiencies are associated with low TFPI levels in plasma
7. Circulating microparticles in deficiency of the natural anticoagulants: OR172
8. The incidence of VTE in asymptomatic carriers of a deficiency of at, PC OR PS: a prospective cohort study: OR078
9. PO-30 Inherited deficiency of antithrombin, protein C or protein S is associated with an increased risk of cancer at a younger age
10. The risk of first venous thromboembolism during pregnancy and puerperium in double heterozygotes for factor V Leiden and prothrombin G20210A
11. The G20210A prothrombin variant and the risk of venous thromboembolism or fetal loss in pregnant women: a family study
12. Differential effects of high prothrombin levels on thrombin generation depending on the cause of the hyperprothrombinemia
13. Long Term Use of Oral Contraceptives Without Thrombosis in Patients with FV Leiden Polymorphism: A Study of 37 Patients (2 Homozygous and 35 Heterozygous)
14. Plasma thrombin generation and circulating nucleosomes in women with early abortions: PO 218
15. Effect of prophylaxis with LMWH on implantation in women undergoing assisted reproductive procedures (IVF or ICSI): an interim report of a prospective randomized study: PB 3.65–6
16. FIX-Padua increases fibrinolytic resistance through a TAFI-mediated mechanism: PB 2.72–1
17. Not all factor V Leiden or prothrombin G20210A mutations are equal: results from a retrospective cohort family study: PA 4.18–5
18. FV Leiden pseudo-homozygotes have a more pronounced hypercoagulable state than homozygotes due to low plasma TFPI levels: O-TH-041
19. Factor V Leiden pseudo-homozygotes have a more pronounced hypercoagulable state than factor V Leiden homozygotes
20. Effect of prothrombin 19911 A>G polymorphism on the risk of cerebral sinus-venous thrombosis
21. Hereditary deficiency of natural inhibitors of coagulation (antitrombin, protein C or protein S) confers increased risk of arterial thromboembolic events. results from a prospective family cohort study: OC-TH-026
22. A risk assessment model for the identification of hospitalized medical patients at risk of venous thromboembolism: OC-MO-049
23. Type III protein S deficiency is associated with a hypercoagulable state and an increased risk of venous thrombosis: OC-MO-005
24. Low-molecular-weight heparin for prevention of obstetric complications in carriers of factor V Leiden or PT-G20210A mutation: AS-WE-023
25. 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): PL-TU-004
26. Duration of anticoagulation and risk of recurrent thromboembolism in carriers of factor V Leiden or prothrombin mutation
27. Factor V Leiden is associated with more distal location of deep vein thrombosis of the leg
28. Immobilization resulting from chronic medical diseases: a new risk factor for recurrent venous thromboembolism in anticoagulated patients
29. D-dimer as an adjunct to compression ultrasonography in patients with suspected recurrent deep vein thrombosis
30. Expression of the normal factor V allele modulates the APC resistance phenotype in heterozygous carriers of the factor V Leiden mutation
31. The incidence of venous thromboembolism in carriers of antithrombin, protein C or protein S deficiency associated with the HR2 haplotype of factor V: a family cohort study
32. Megakaryocytes endocytose and subsequently modify human factor V in vivo to form the entire pool of a unique platelet-derived cofactor
33. The G20210A prothrombin gene mutation: is there room for screening families?
34. Screening for thrombophilia in children: a puzzling decision with unclear implications
35. Seasonal Variation in the Incidence of Deep Vein Thrombosis in Patients With Deficiency of Protein C or Protein S
36. O007: Type of combined contraceptives and the risk of venous thromboembolism in antithrombin, protein C and protein S deficient women: a prospective cohort study
37. Factor V Leiden and prothrombin gene mutation in inflammatory bowel disease in Mediterranean area
38. The incidence of VTE in asymptomatic carriers of a deficiency of at, PC OR PS: a prospective cohort study
39. High vs. low doses of low‐molecular‐weight heparin for the treatment of superficial vein thrombosis of the legs: a double‐blind, randomized trial
40. Aspirin for preventing the recurrence of venous thromboembolism
41. 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
42. Circulating microparticles in carriers of factor V Leiden mutation
43. Factor IX activity/antigen ratio and the risk of unprovoked venous thrombosis
44. FRI0563 Detection of IGG Anti-Domain I Beta2 Glycoprotein I Antibodies by Chemiluminescence Immunoassay in Primary Antiphospholipid Syndrome
45. Erratum to Similar hypercoagulable state and thrombosis risk in type I and type III protein S-deficient individuals from mixed type I/III
46. Screening for thrombophilia and antithromboticprophylaxis in pregnancy: Guidelines of the Italian Society for Haemostasis andThrombosis (SISET)
47. Type III protein S deficiency is associated with a hypercoagulable state and an increased risk of venous thrombosis
48. Thrombophilia does not increase the risk of the post-thrombotic syndrome. A prospective cohort study
49. Objectives and methodology: Guidelines of the ItalianSociety for Haemostasis and Thrombosis (SISET)
50. Thrombin generation in carriers of inheroted clotting inhibitors defects
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