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3. No changes in hemostasis after COVID-19–heterologous vaccination schedule: A subanalysis of the phase 2 CombiVacS study

6. Moving towards Normalization of haemostasis and health equity: Evolving treatment goals for haemophilia A.

9. Management of acquired hemophilia A: results from the Spanish registry

10. Humanistic burden of haemophilia A without inhibitors: A cross‐sectional analysis of the HemoLIFE study.

12. Knee replacement surgery in a patient with acquired von Willebrand disease: a case study with recommendations for patient management

17. A post hoc comparative real‐world analysis of HEAD‐US score for joint health assessment of patients with severe haemophilia A and B in Spain.

20. Study of platelet kinetics in immune thrombocytopenia to predict splenectomy response

21. Recommendations for the Clinical Approach to Immune Thrombocytopenia: Spanish ITP Working Group (GEPTI)

22. Comparative analysis of Hemophilia Early Arthropathy Detection with Ultrasound (HEAD-US) scores in persons with nonsevere hemophilia A and B reveals a high degree of joint damage in both disease types

23. Interim analyses of the multinational real‐world prospective cohort HEM‐POWR study evaluating the effectiveness and safety of damoctocog alfa pegol in patients with hemophilia A.

24. Study of platelet kinetics in immune thrombocytopenia to predict splenectomy response.

28. Recommendations for the Clinical Approach to Immune Thrombocytopenia: Spanish ITP Working Group (GEPTI)

29. Long-acting recombinant coagulation factor IX albumin fusion protein (rIX-FP) in hemophilia B: results of a phase 3 trial

30. No changes in haemostasis after COVID-19-heterologous vaccination schedule: a sub analysis of the phase 2 CombiVacS study

33. Eptacog Beta Efficacy in Treating Mild or Moderate Bleeds in Target Joints of Individuals with Hemophilia A or B and Inhibitors in PERSEPT 1

34. Predictive Value of Platelet Sequestration Studies in Splenectomy Response

35. Rozrolimupab, a mixture of 25 recombinant human monoclonal RhD antibodies, in the treatment of primary immune thrombocytopenia

38. The factor VIII treatment history of non‐severe hemophilia A: COMMENT. Joint damage in adult patients with mild or moderate hemophilia A evaluated with the HEAD‐US system

40. Successful discontinuation of eltrombopag after complete remission in patients with primary immune thrombocytopenia

42. Expert opinion paper on the treatment of hemophilia B with albutrepenonacog alfa

46. Avatrombopag in Immune Thrombocytopenia (ITP). Real-Life Experience of Its Use in Hospitals within the Community of Madrid, Spain (AVAMAD STUDY)

47. The Importance of Platelet Glycoside Residues in the Haemostasis of Patients with Immune Thrombocytopaenia

48. Ultrasound evaluation of joint damage and disease activity in adult patients with severe haemophilia A using the HEAD‐US system

49. COVID‐19 and telemedicine in haemophilia in a patient with severe haemophilia A and orthopaedic surgery

50. Insights into the Procoagulant Profile of Patients with Systemic Lupus Erythematosus without Antiphospholipid Antibodies

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