All Stories

  1. Obesity in the global haemophilia population: prevalence, implications and expert opinions for weight management
  2. Updates from guardian™: a comprehensive registration programme
  3. Long‐term patterns of safety and efficacy of bleeding prophylaxis with turoctocog alfa (NovoEight ® ) in previously treated patients with severe haemophilia A: interim results of the guardian ™ 2 extensio...
  4. Recombinant activated factor VII in the treatment of bleeds and for the prevention of surgery-related bleeding in congenital haemophilia with inhibitors
  5. Allergic reaction in a cohort of haemophilia A patients using plasma-derived factor VIII (FVIII) concentrate is rare and not necessarily triggered by FVIII
  6. A longitudinal evaluation of anti-FVIII antibodies demonstrated IgG4 subclass is mainly correlated with high-titre inhibitor in haemophilia A patients
  7. Impact of severe haemophilia A on patients' health status: results from the guardian ™ 1 clinical trial of turoctocog alfa (NovoEight ® )
  8. Switching to recombinant factor IX Fc fusion protein prophylaxis results in fewer infusions, decreased factor IX consumption and lower bleeding rates
  9. Long‐acting recombinant factor IX Fc fusion protein ( rFIXF c) for perioperative management of subjects with haemophilia B in the phase 3 B‐LONG study
  10. Systematic Analysis of Bleeding Phenotype in PT-VWD Compared to Type 2B VWD Using an Electronic Bleeding Questionnaire
  11. Safety and efficacy of cryoprecipitate-poor plasma as a replacement fluid for therapeutic plasma exchange in thrombotic thrombocytopenic purpura: A single center retrospective evaluation
  12. Omental implantation of BOECs in hemophilia dogs results in circulating FVIII antigen and a complex immune response
  13. Development of a serious game for children with hemophilia
  14. Musculoskeletal evaluation in severe haemophilia A patients from Latin America
  15. Phase 3 Study of Recombinant Factor IX Fc Fusion Protein in Hemophilia B
  16. Increased adhesive and inflammatory properties in blood outgrowth endothelial cells from sickle cell anemia patients
  17. Results from a large multinational clinical trial (guardian™3) using prophylactic treatment with turoctocog alfa in paediatric patients with severe haemophilia A: safety, efficacy and pharmacokinetics
  18. A novel use of thromboelastography in type 2B von Willebrand disease
  19. Establishing a harmonized haemophilia registry for countries with developing health care systems
  20. Surgery in patients with hemophilia: Is thromboprophylaxis mandatory?
  21. Factor VIII inhibitors in patients with congenital severe haemophilia A and its relation to genotype
  22. Meeting the challenges of haemophilia care and patient support in China and Brazil
  23. Non-operative management of blunt major hepatic injury in a young adult with severe haemophilia A
  24. Brain plasticity for verbal and visual memories in patients with mesial temporal lobe epilepsy and hippocampal sclerosis: An fMRI study
  25. Evaluation of the host response to endotoxemia of FVIII and FIX deficient mice
  26. A MicroRNA-regulated and GP64-pseudotyped Lentiviral Vector Mediates Stable Expression of FVIII in a Murine Model of Hemophilia A
  27. Frequency of Platelet type versus Type 2B von Willebrand Disease
  28. Eradication of neutralizing antibodies to factor VIII in canine hemophilia A after liver gene therapy
  29. VKORC1 V66M mutation in African Brazilian patients resistant to oral anticoagulant therapy
  30. Long-term prospective study of recurrent venous thromboembolism in a Hispanic population
  31. Unique strategies for therapeutic gene transfer in haemophilia A and haemophilia B
  32. Simultaneous bleeding and thrombosis in superwarfarin poisoning
  33. Reduction of the immune response to factor VIII mediated through tolerogenic factor VIII presentation by immature dendritic cells
  34. Molecular Genetic Testing of Hemostasis and Thrombosis in Developing Countries: Achievements, Hopes, and Challenges
  35. Polymorphisms of methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MTR), methionine synthase reductase (MTRR), and thymidylate synthase (TYMS) in multiple myeloma risk
  36. Efficacy and safety of dapsone as a second-line treatment in non-splenectomized adults with immune thrombocytopenic purpura
  37. A cost evaluation of treatment alternatives for mild-to-moderate bleeding episodes in patients with haemophilia and inhibitors in Brazil
  38. Association between estrogen receptor alpha and beta gene polymorphisms and deep vein thrombosis
  39. Evidence of Multiyear Factor IX Expression by AAV-Mediated Gene Transfer to Skeletal Muscle in an Individual with Severe Hemophilia B
  40. An inherited mutation leading to production of only the short isoform of GATA-1 is associated with impaired erythropoiesis
  41. Early in vivo anticoagulation inhibits the angiogenic response following hindlimb ischemia in a rodent model
  42. Clinical Impact of Oral Health Indexes in Dental Extraction of Hemophilic Patients
  43. Erratum: CORRIGENDUM: Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response
  44. Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response
  45. Use of recombinant factor VIIa in the management of severe bleeding episodes in patients with Bernard–Soulier syndrome
  46. What is a cure and how do we get there?
  47. Genetic variability of platelet glycoprotein Ibα gene
  48. Platelet glycoprotein Ibα polymorphisms modulate the risk for myocardial infarction
  49. Effects of high platelet concentration in collecting and freezing dry platelets concentrates
  50. Rapid detection of the prothrombin C20209T variant by differential sensitivity to restriction endonuclease digestion
  51. AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B
  52. The impact of the search for thrombophilia risk factors among antiphospholipid syndrome patients with thrombosis
  53. Possible Association between Cytomegalovirus Infection and Gastrointestinal Bleeding in Hemophiliac Patients
  54. Inherited Risk Factors for Thrombophilia Among Children with Legg-Calvé-Perthes Disease
  55. 82 Megakaryopoiesis in myelodysplastic syndromes: Morphological and immunocytochemical features