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

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

3. Impact of hemophilia B on quality of life in affected men, women, and caregivers—Assessment of patient‐reported outcomes in the B‐HERO‐S study. (11th April 2018)

5. Impact of mild to severe hemophilia on engagement in recreational activities by US men, women, and children with hemophilia B: The Bridging Hemophilia B Experiences, Results and Opportunities into Solutions (B‐HERO‐S) study. (April 2017)

6. Management of US men, women, and children with hemophilia and methods and demographics of the Bridging Hemophilia B Experiences, Results and Opportunities into Solutions (B‐HERO‐S) study. (April 2017)

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)