All Stories

  1. Switching patients in the age of long-acting recombinant products?
  2. Haemophilia clinical care and research needs: Assessing priorities
  3. McMaster RARE-Bestpractices clinical practice guideline on diagnosis and management of the catastrophic antiphospholipid syndrome
  4. Pharmacokinetics and the transition to extended half-life factor concentrates: communication from the SSC of the ISTH
  5. Focusing in on use of pharmacokinetic profiles in routine hemophilia care
  6. Performing and interpreting individual pharmacokinetic profiles in patients with Hemophilia A or B: Rationale and general considerations
  7. Core outcome set for gene therapy in haemophilia: Results of the coreHEM multistakeholder project
  8. Past, present and future of haemophilia gene therapy: From vectors and transgenes to known and unknown outcomes
  9. Comorbidities in persons with haemophilia aged 60 years or more compared with age-matched people from the general population
  10. Estimating and interpreting the pharmacokinetic profiles of individual patients with hemophilia A or B using a population pharmacokinetic approach: communication from the SSC of the ISTH
  11. Minimal dataset for post-registration surveillance of new drugs in hemophilia: communication from the SSC of the ISTH
  12. Switching to extended half-life products in Canada - preliminary data
  13. Association of body weight with efficacy and safety outcomes in phase III randomized controlled trials of direct oral anticoagulants: a systematic review and meta‐analysis
  14. Population PK tailoring in hemophilia
  15. Large scale studies assessing anti-factor VIII antibody development in previously untreated haemophilia A: what has been learned, what to believe and how to learn more
  16. Indirect comparisons of efficacy and weekly factor consumption during continuous prophylaxis with recombinant factor VIII Fc fusion protein and conventional recombinant factor VIII products
  17. Research and policy implications of a recently published controlled study in previously untreated haemophilia patients at high risk of inhibitor development
  18. Natural history and clinical characteristics of inhibitors in previously treated haemophilia A patients: a case series
  19. Measuring the quality of haemophilia care across different settings: a set of performance indicators derived from demographics data
  20. Interpreting trial sequential analysis
  21. Bayesian approach to the assessment of the population-specific risk of inhibitors in hemophilia A patients: a case study
  22. Recommendations for authors of manuscripts reporting inhibitor cases developed in previously treated patients with hemophilia: communication from the SSC of the ISTH
  23. Methodology for the development of the NHF-McMaster Guideline on Care Models for Haemophilia Management
  24. Care models in the management of haemophilia: a systematic review
  25. NHF-McMaster Guideline on Care Models for Haemophilia Management
  26. Integrated multidisciplinary care for the management of chronic conditions in adults: an overview of reviews and an example of using indirect evidence to inform clinical practice recommendations in the field of rare diseases
  27. Recombinant factor VIIa concentrate versus plasma-derived concentrates for treating acute bleeding episodes in people with haemophilia and inhibitors