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List of works by Michelle Witkop

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.

scientific article published in April 2018

Building the blueprint: Formulating a community‐generated national plan for future research in inherited bleeding disorders

scientific article published in 2022

Correlations between patient-reported outcomes and self-reported characteristics in adults with hemophilia B and caregivers of children with hemophilia B: analysis of the B-HERO-S study

scientific article published on 18 September 2019

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

scientific article published on 5 March 2018

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.

scientific article published on April 2017

Impact of pain and functional impairment in US adults with haemophilia: Patient-reported outcomes and musculoskeletal evaluation in the pain, functional impairment and quality of life (P-FiQ) study.

scientific article published on 8 December 2017

Interrelationship between depression, anxiety, pain, and treatment adherence in hemophilia: results from a US cross-sectional survey

scientific article published on 20 September 2019

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.

scientific article published on April 2017

Natural history study of factor IX deficiency with focus on treatment and complications (B-Natural)

scientific article published on 05 December 2020

Patient advocacy and its importance to laboratory medicine practice: A response from patient advocacy groups

scientific article published on 01 June 2020

Patient, caregiver, and provider perceptions of pain and pain management in adolescents and young adults with bleeding disorders.

scientific article published on 14 August 2017

Patient-reported outcomes and joint status across subgroups of US adults with hemophilia with varying characteristics: Results from the Pain, Functional Impairment, and Quality of Life (P-FiQ) study.

scientific article published in April 2018

Reliability and validity of patient-reported outcome instruments in US adults with hemophilia B and caregivers in the B-HERO-S study

scientific article published on 19 October 2018

Self-reported prevalence, description and management of pain in adults with haemophilia: methods, demographics and results from the Pain, Functional Impairment, and Quality of life (P-FiQ) study.

scientific article published on 16 April 2017

The viability and necessity of APRN-led care models in the clinical management of haemophilia and other inherited bleeding and clotting disorders

scientific article published on 26 June 2018

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