255 results on '"Stasko, Jan"'
Search Results
2. Diagnostic value of clot formation parameters determined by rotational thromboelastometry in 63 patients with congenital dysfibrinogenemia
3. Platelet miRNA Expression in Patients with Sticky Platelet Syndrome
4. Ixazomib, lenalidomide, and dexamethasone combination in “real-world” clinical practice in patients with relapsed/refractory multiple myeloma
5. Bleeding in Patients with Antiphospholipid Antibodies
6. Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop)
7. Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia
8. Does type 2 diabetes affect the on-treatment levels of direct oral anticoagulants in patients with atrial fibrillation?
9. Basic Principles of Rotational Thromboelastometry (ROTEM®) and the Role of ROTEM—Guided Fibrinogen Replacement Therapy in the Management of Coagulopathies
10. A Functional Assay for the Determination of Heparin-Induced Thrombocytopenia via Flow Cytometry
11. Perioperative Monitoring with Rotational Thromboelastometry in a Severe Hemophilia A Patient Undergoing Elective Ankle Surgery.
12. Perioperative Monitoring with Rotational Thromboelastometry in a Severe Hemophilia A Patient Undergoing Elective Ankle Surgery
13. Association of Genetic Variability in Selected Genes with Platelet Hyperaggregability and Arterial Thrombosis
14. Basic Principles of Rotational Thromboelastometry (ROTEM ®) and the Role of ROTEM—Guided Fibrinogen Replacement Therapy in the Management of Coagulopathies.
15. Differential mRNA expression of the main apoptotic proteins in normal and malignant cells and its relation to in vitro resistance
16. Successful Use of a Highly Purified Plasma von Willebrand Factor Concentrate Containing Little FVIII for the Long-Term Prophylaxis of Severe (Type 3) von Willebrandʼs Disease
17. Platelet aggregation abnormalities in patients with fetal losses: the GP6 gene polymorphism
18. Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing
19. Progress in the Understanding of Sticky Platelet Syndrome
20. Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia
21. Heterogeneity of Genotype–Phenotype in Congenital Hypofibrinogenemia—A Review of Case Reports Associated with Bleeding and Thrombosis
22. A new decade awaits sticky platelet syndrome: where are we now, how do we manage and what are the complications?
23. How can Secondary Thromboprophylaxis in High-Risk Pregnant Patients be Improved?
24. Novel Fibrinogen Bbeta Chain Mutation as an Underlying Mechanism of Afibrinogenemia?
25. Different Models of Inheritance in Selected Genes in Patients with Sticky Platelet Syndrome and Fetal Loss
26. Multimer Analysis of Von Willebrand Factor in Von Willebrand Disease with a Hydrasys Semi-Automatic Analyzer—Single-Center Experience
27. Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management
28. Ixazomib, lenalidomide, and dexamethasone combination in “real-world” clinical practice in patients with relapsed/refractory multiple myeloma
29. Assessing the hemostasis with thromboelastometry in direct oral anticoagulants-treated patients with atrial fibrillation
30. Sticky Platelet Syndrome: History and Future Perspectives*
31. Perioperative management of a severe congenital hypofibrinogenemia with thrombotic phenotype
32. Genetic Background of Inherited Factor XIII-A Subunit Deficiency: Review of the Literature and Description of Two New Cases
33. A
34. COVID19 infection in a patient with paroxysmal nocturnal hemoglobinuria
35. How Can Rotational Thromboelastometry as a Point-of-Care Method Be Useful for the Management of Secondary Thromboprophylaxis in High-Risk Pregnant Patients?
36. Sticky Platelet Syndrome
37. Type 2 Diabetes and Fibrinolysis
38. Use of Fibrinogen Determination Methods in Differential Diagnosis of Hypofibrinogenemia and Dysfibrinogenemia
39. Impact of Dabigatran Treatment on Rotation Thromboelastometry
40. A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype
41. Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype
42. Edoxaban affects TRAP-dependent platelet aggregation
43. Impact of Edoxaban on Thrombin-Dependent Platelet Aggregation
44. Successful immune tolerance induction consisting of high-dose factor VIII rich in von Willebrand factor and pulsed intravenous immunoglobulin: a case report
45. Genetic Background of von Willebrand Disease: History, Current State, and Future Perspectives
46. Comment on: Inherited Thrombophilia and Pregnancy Complications: Should We Test?
47. Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop)
48. Anticoagulation therapy in Slovakia
49. Erythropoietin and granulocyte colony-stimulating factor increase plasminogen activator inhibitor-1 release in HUVEC culture
50. Sticky Platelet Syndrome: 35 Years of Growing Evidence
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.