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You searched for: Author/Creator Curtis, Randall

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1. Association of factor expression levels with health-related quality of life and direct medical costs for people with haemophilia B. (31st December 2022)

2. Challenges in transition to adulthood for young adult patients with hemophilia: Quantifying the psychosocial issues and developing solutions. (December 2015)

3. Evaluation of the sexual health in people living with hemophilia. Issue 6 (19th September 2021)

4. Exploring regional variations in the cross‐cultural, international implementation of the Patient Reported Outcomes Burdens and Experience (PROBE) study. Issue 3 (12th March 2019)

5. Humanistic burden of problem joints for children and adults with haemophilia. Issue 2 (27th December 2022)

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

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

9. Test‐retest properties of the Patient Reported Outcomes, Burdens and Experiences (PROBE) questionnaire and its constituent domains. Issue 1 (6th December 2018)

10. Treatment outcomes, quality of life, and impact of hemophilia on young adults (aged 18–30 years) with hemophilia. (December 2015)