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21. Patient preferences and priorities for haemophilia gene therapy in the US: A discrete choice experiment. Issue 5 (26th July 2021)

22. Patient‐relevant health outcomes for hemophilia care: Development of an international standard outcomes set. Issue 4 (6th March 2021)

25. Physical activity, physical fitness and cardiometabolic risk amongst adults with moderate and severe haemophilia. Issue 1 (4th October 2022)

27. Psychometric properties of the Patient Reported Outcomes, Burdens and Experiences (PROBE) questionnaire. Issue 8 (8th August 2018)

29. Recombinant factor IX‐Fc fusion protein in severe hemophilia B: Patient‐reported outcomes and health‐related quality of life. Issue 7 (11th October 2021)

30. Telehealth for delivery of haemophilia comprehensive care during the COVID‐19 pandemic. Issue 6 (30th September 2020)