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1. A study of dedicated haemophilia carrier clinics in the United States: Prevalence, services offered and barriers to development. Issue 5 (14th June 2020)

2. Adult lifetime cost of hemophilia B management in the US: payer and societal perspectives from a decision analytic model. (1st January 2021)

3. Assessments of pain, functional impairment, anxiety, and depression in US adults with hemophilia across patient‐reported outcome instruments in the Pain, Functional Impairment, and Quality of Life (P‐FiQ) study. (2nd March 2018)

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

7. Bleeding events and safety outcomes in persons with haemophilia A with inhibitors: A prospective, multi‐centre, non‐interventional study. Issue 6 (8th October 2018)

9. Community counts: Evolution of a national surveillance system for bleeding disorders. Issue 6 (28th April 2018)

10. Cover Image. Issue 6 (13th November 2021)