All Stories

  1. Health education and empowerment in adult patients with haemophilia
  2. A randomized trial of safety, pharmacokinetics and pharmacodynamics of concizumab in people with hemophilia A
  3. Recommendations on multidisciplinary management of elective surgery in people with haemophilia
  4. Head trauma in the haemophilic child and management in a paediatric emergency department: Descriptive study
  5. Immune thrombocytopenia - in defence of the platelet count. Response to Hill
  6. Outcome measures for adult and pediatric hemophilia patients with inhibitors
  7. Long-term outcome of haemophilia A patients after successful immune tolerance induction therapy using a single plasma-derived FVIII/VWF product: the long-term ITI study
  8. Clinical overview of Fanhdi/Alphanate (plasma-derived, VWF-containing FVIII concentrate) in immune tolerance induction in haemophilia A patients with inhibitors
  9. Arthroscopic debridement for ankle haemophilic arthropathy
  10. The pharmacokinetics of a B-domain truncated recombinant factor VIII, turoctocog alfa (NovoEight® ), in patients with hemophilia A
  11. Adherence to prophylaxis and quality of life in children and adolescents with severe haemophilia A
  12. Light-chain amyloidosis presenting as a change in bleeding phenotype in a patient with mild haemophilia A
  13. Radiosynovectomy in haemophilia: Long-term results of 500 procedures performed in a 38-year period
  14. Adult haemophilia A patients with inhibitors: successful immune tolerance induction with a single FVIII / VWF product
  15. Hematological Concepts and Hematological Perioperative Treatment
  16. The Analgesic Efficacy of a COX-2 Inhibitor (Oral Celecoxib) in Adult Hemophilic Patients and Intense Joint Pain Secondary to Advanced Hemophilic Arthropathy
  17. Switching treatments in haemophilia: is there a risk of inhibitor development?
  18. Effect of thrombopoietin-receptor agonists on a proliferation-inducing ligand (APRIL) plasma levels in patients with immune thrombocytopaenia
  19. Managing Haemophilia for Life: 4th Haemophilia Global Summit
  20. Joint disease, the hallmark of haemophilia: What issues and challenges remain despite the development of effective therapies?
  21. Is radiosynovectomy (RS) effective for joints damaged by haemophilia with articular degeneration in simple radiography (ADSR)?
  22. Efficacy of celecoxib in the treatment of joint pain caused by advanced haemophilic arthropathy in adult patients with haemophilia A
  23. Effects of thrombopoietin receptor agonists on procoagulant state in patients with immune thrombocytopenia
  24. Effects of thrombopoietin receptor agonists on procoagulant state in patients with immune thrombocytopenia
  25. Valoración de la eficacia percibida de la dinamica grupal “¿qué-tal?” Para el autocuidado y aprendizaje mutuo en un equipo asistencial
  26. Joint aspiration of acute tense knee haemarthroses in adult haemophilia A patients
  27. Primary and rescue immune tolerance induction in children and adults: a multicentre international study with a VWF ‐containing plasma‐derived FVIII concentrate
  28. Severe postoperative haemarthrosis following a total knee replacement in a haemophiliac patient caused by a pseudoaneurysm: early treatment with arterial embolization
  29. Rotational thromboelastometry (ROTEM) in Behçet's disease
  30. Femur fracture in a woman with severe factor X deficiency - an experience using factor X concentrate in surgery
  31. Factor VIII gene (F8) mutation and risk of inhibitor development in nonsevere hemophilia A
  32. Radiosynovectomy
  33. Cost-effectiveness of recombinant activated factor VII vs. plasma-derived activated prothrombin complex concentrate in the treatment of mild-to-moderate bleeding episodes in patients with severe haemophilia A and inhibitors in Spain
  34. 2013. Documento Sevilla de Consenso sobre Alternativas a la Transfusión de Sangre Alogénica. Actualización del Documento Sevilla
  35. 2013. Documento Sevilla de Consenso sobre Alternativas a la Transfusión de Sangre Alogénica. Actualización del Documento Sevilla
  36. Platelet apoptosis and agonist-mediated activation in myelodysplastic syndromes
  37. Novel coagulation factor concentrates: Issues relating to their clinical implementation and pharmacokinetic assessment for optimal prophylaxis in haemophilia patients
  38. Third Åland islands conference on von Willebrand disease, 26-28 September 2012: meeting report
  39. Behçet’s disease: new insight into the relationship between procoagulant state, endothelial activation/damage and disease activity
  40. Effective prophylaxis with rFVIIa in young haemophiliacs with inhibitors using a schedule similar to FVIII prophylaxis in non-inhibitor patients
  41. PRO-PACT: Retrospective observational study on the prophylactic use of recombinant factor VIIa in hemophilia patients with inhibitors
  42. Efficacy of factor IX Grifols® in surgery: experience of an international multicentre retrospective study
  43. Management of delivery with FVIII/VWF concentrates in a pregnant woman with type 3 von Willebrand disease and alloantibodies
  44. Optimizing joint function: new knowledge and novel tools and treatments
  45. An uncommon cause of elbow synovitis in an adult haemophilia patient
  46. F8 gene dosage defects in atypical patients with severe haemophilia A
  47. A complex case of infected total knee arthroplasty in a haemophilic patient with inhibitor
  48. Is on-demand treatment effective in patients with severe haemophilia?
  49. Iatrogenic fracture of the proximal tibia as a complication of knee manipulation under anaesthesia in a haemophilia patient with an ipsilateral stiff knee secondary to a supracondylar non-union of the femur
  50. Management of bleeding disorders in adults
  51. Platelet soluble CD40L and matrix metalloproteinase 9 activity are proinflammatory mediators in Behçet disease patients
  52. Pharmacokinetic properties of two different recombinant activated factor VII formulations
  53. Liver transplantation in Spanish haemophiliacs
  54. Joint protection in haemophilia
  55. Late avascular necrosis of the femoral head (anfh) after the percutaneous fixation of a non-displaced fracture of the femoral neck in a haemophilic patient with inhibitors: a non-reported association
  56. An uncommon cause of knee haemarthrosis in an adult haemophilia patient suffering from long-term paraplegia
  57. Prophylaxis in Adults with Hemophilia
  58. Initial and Advanced Stages of Hemophilic Arthropathy, and Other Musculo-Skeletal Problems: The Role of Orthopedic Surgery
  59. Current and Future Approaches to Gene Therapy in Patients with Hemophilia
  60. Radiosynovectomy in hemophilia: quantification of its effectiveness through the assessment of 10 articular parameters
  61. Radiosynovectomy in patients with chronic haemophilic synovitis: when is more than one injection necessary?
  62. Infection after total knee arthroplasty in haemophilic arthropathy with special emphasis on late infection
  63. What patient, joint and isotope characteristics influence the response to radiosynovectomy in patients with haemophilia?
  64. When should prophylaxis therapy in inhibitor patients be considered?
  65. Focusing on haemophilia B: prophylaxis in Spanish patients
  66. Prophylaxis therapy in haemophilia A: current situation in Spain
  67. Improving Type 1 Diabetes After Treatment of Immune Thrombocytopenia With Rituximab: Killing Two Birds With One Stone
  68. Clinical and genetic findings in five female patients with haemophilia A: Identification of a novel missense mutation, p.Phe2127Ser
  69. Paediatric haemophilia with inhibitors: existing management options, treatment gaps and unmet needs
  70. Possible role for cellular FXIII in monocyte-derived dendritic cell motility
  71. The role of selective angiographic embolization of the musculo-skeletal system in haemophilia
  72. New insights into the expression and role of platelet factor XIII-A
  73. Haemophilia in Spain
  74. Surgery in haemophilia patients with inhibitors, with special emphasis on orthopaedics: Madrid experience
  75. Prophylaxis in 10 patients with severe haemophilia A and inhibitor: different approaches for different clinical situations
  76. Review: Factor XI Deficiency: Review and Management in Pregnant Women
  77. Orthopaedic surgery in haemophilia patients with inhibitors as the last resort
  78. Experiences in the prevention of arthropathy in haemophila patients with inhibitors
  79. Prevention of haemophilic arthropathy during childhood. May common orthopaedic management be extrapolated from patients without inhibitors to patients with inhibitors?
  80. “Primary prophylaxis” with rFVIIa in a patient with severe haemophilia a and inhibitor
  81. Clinical efficacy in bleeding and surgery in von Willebrand patients treated with Fanhdi®a highly purified, doubly inactivated FVIII/VWF concentrate
  82. Acquired von Willebrand syndrome
  83. Controversies and Challenges in Elective Orthopedic Surgery in Patients With Hemophilia and Inhibitors
  84. Management of the Delivery in Pregnant Women with Severe Factor XI Deficiency
  85. Haemoperitoneum in a female patient with haemophilia A caused by a ruptured ovarian follicle
  86. Orthopaedic surgery for inhibitor patients: a series of 27 procedures (25 patients)
  87. Rituximab in the management of chronic immune thrombocytopenic purpura: an effective and safe therapeutic alternative in refractory patients
  88. Rituximab in the management of chronic immune thrombocytopenic purpura: an effective and safe therapeutic alternative in refractory patients
  89. Psychometric field study of the new haemophilia quality of life questionnaire for adults: The 'Hemofilia-QoL'
  90. Prophylactic treatment effects on inhibitor risk: experience in one centre
  91. Surgery in haemophilic patients with inhibitor: 20 years of experience
  92. Acquired Haemophilia: Review and Meta-Analysis Focused on Therapy and Prognostic Factors
  93. Analysis of the causes of immediate unanticipated bleeding after pediatric adenotonsillectomy
  94. Otolaryngologic Surgery in Children With von Willebrand Disease
  95. Acquired hemophilia: a single-center survey with emphasis on immunotherapy and treatment-related side-effects
  96. Successful thyroidectomy in a patient with Hermansky–Pudlak syndrome treated with recombinant activated factor VII and platelet concentrates
  97. Induction of a Hypercoagulability State and Endothelial Cell Activation by Granulocyte Colony-Stimulating Factor in Peripheral Blood Stem Cell Donors
  98. The use of haemostatic drugs in haemophilia: desmopressin and antifibrinolytic agents
  99. Complications of central venous catheters in patients with haemophilia and inhibitors
  100. Yttrium-90 synoviorthesis for chronic haemophilic synovitis: Madrid experience
  101. Continuous infusion of recombinant activated factor VII during caesarean section delivery in a patient with congenital factor VII deficiency
  102. A prospective randomized trial of granulocyte colony-stimulating factor therapy after autologous blood stem cell transplantation in adults
  103. Erratum: Case report: Haploidentical peripheral blood stem cell transplantation with a combination of CD34 selection and T cell depletion as graft-versus-host disease prophylaxis in a patient with severe combined immunodeficiency
  104. Hematopoietic cell transplantation using plasma and DMSO without HES, with non-programmed freezing by immersion in a methanol bath: results in 213 cases
  105. Haploidentical peripheral blood stem cell transplantation with a combination of CD34 selection and T cell depletion as graft-versus-host disease prophylaxis in a patient with severe combined immunodeficiency
  106. Haemophilia A and chronic hepatopathy caused by extrahepatic biliary atresia: two congenital diseases cured by orthotopic liver transplantation
  107. Posttransplant CD30 (Ki-1)–Positive Anaplastic Large Cell Lymphoma
  108. Osteonecrosis of the Femoral Head
  109. Haematological Substitutive Treatment of Haemophilic Haemarthroses
  110. General Medical Management of Bleeding Episodes: Haemarthroses, Muscle Haematomas, Mucocutaneous Bleeding and Haematuria