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Known-group validity of patient-reported outcome instruments and hemophilia joint health score v2.1 in US adults with hemophilia: results from the Pain, Functional Impairment, and Quality of life (P-FiQ) study.
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- Patient Preference & Adherence, 2017, v. 11, p. 1745, doi. 10.2147/PPA.S141392
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- Article
Reliability of patient-reported outcome instruments in US adults with hemophilia: the Pain, Functional Impairment and Quality of life (P-FiQ) study.
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- Patient Preference & Adherence, 2017, v. 11, p. 1603, doi. 10.2147/PPA.S141389
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Racial and Ethnic Differences in Distress, Depression, and Quality of Life in people with hemophilia.
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- Journal of Racial & Ethnic Health Disparities, 2024, v. 11, n. 3, p. 1394, doi. 10.1007/s40615-023-01616-3
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Complete Spontaneous Remission of Diffuse Large B-Cell Lymphoma of the Maxillary Sinus After Concurrent Infections.
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- Clinical Lymphoma, Myeloma & Leukemia, 2012, v. 12, n. 6, p. 455, doi. 10.1016/j.clml.2012.06.007
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Reliability and validity of patient‐reported outcome instruments in US adults with hemophilia B and caregivers in the B‐HERO‐S study.
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- European Journal of Haematology, 2018, v. 101, n. 6, p. 781, doi. 10.1111/ejh.13168
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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.
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- European Journal of Haematology, 2018, v. 100, n. 6, p. 592, doi. 10.1111/ejh.13055
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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.
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- European Journal of Haematology, 2018, v. 100, p. 14, doi. 10.1111/ejh.13028
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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.
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- European Journal of Haematology, 2018, v. 100, p. 5, doi. 10.1111/ejh.13027
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What can we learn from using formal patient‐reported outcome instruments to assess pain, functional impairment, anxiety, and depression in US adults with hemophilia?
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- European Journal of Haematology, 2018, v. 100, p. 3, doi. 10.1111/ejh.13026
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Factors associated with pain severity, pain interference, and perception of functional abilities independent of joint status in US adults with hemophilia: Multivariable analysis of the Pain, Functional Impairment, and Quality of Life (P‐FiQ) study.
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- European Journal of Haematology, 2018, v. 100, p. 25, doi. 10.1111/ejh.13025
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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.
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- European Journal of Haematology, 2017, v. 98, p. 5, doi. 10.1111/ejh.12854
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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.
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- Patient Related Outcome Measures, 2019, v. 10, p. 299, doi. 10.2147/PROM.S219166
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Prophylaxis for children with moderate hemophilia: Use of a guideline to increase early initiation.
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- Pediatric Blood & Cancer, 2021, v. 68, n. 1, p. 1, doi. 10.1002/pbc.28577
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Patterns of symptoms and functional impairments in children with cancer.
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- Pediatric Blood & Cancer, 2014, v. 61, n. 7, p. 1282, doi. 10.1002/pbc.25029
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Effect of etranacogene dezaparvovec on quality of life for severe and moderately severe haemophilia B participants: Results from the phase III HOPE‐B trial 2 years after gene therapy.
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- Haemophilia, 2024, v. 30, n. 3, p. 709, doi. 10.1111/hae.14977
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Matching‐adjusted indirect comparison of bleeding outcomes in severe haemophilia A: Comparing valoctocogene roxaparvovec gene therapy, emicizumab prophylaxis, and FVIII replacement prophylaxis.
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- Haemophilia, 2023, v. 29, n. 4, p. 1087, doi. 10.1111/hae.14818
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Cross‐sectional study evaluating the association of haemophilia‐related distress and clinically relevant outcomes.
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- Haemophilia, 2023, v. 29, n. 2, p. 505, doi. 10.1111/hae.14741
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Physical therapy within US HTCs: A multicentre survey of utilization, practice patterns and pain management approaches.
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- Haemophilia, 2022, v. 28, n. 2, p. 343, doi. 10.1111/hae.14501
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Shortening the Haemophilia Activities List (HAL) from 42 items to 18 items.
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- Haemophilia, 2021, v. 27, n. 6, p. 1062, doi. 10.1111/hae.14408
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Women and girls with haemophilia receiving care at specialized haemophilia treatment centres in the United States.
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- Haemophilia, 2021, v. 27, n. 6, p. 1037, doi. 10.1111/hae.14403
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Patient preferences and priorities for haemophilia gene therapy in the US: A discrete choice experiment.
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- Haemophilia, 2021, v. 27, n. 5, p. 769, doi. 10.1111/hae.14383
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An evaluation of PROMIS health domains in adults with haemophilia: A cross‐sectional study.
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- Haemophilia, 2021, v. 27, n. 3, p. 375, doi. 10.1111/hae.14321
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Evidence of a disability paradox in patient‐reported outcomes in haemophilia.
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- Haemophilia, 2021, v. 27, n. 2, p. 245, doi. 10.1111/hae.14278
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Outcome measures in Haemophilia: Beyond ABR (Annualized Bleeding Rate).
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- Haemophilia, 2021, v. 27, p. 87, doi. 10.1111/hae.14099
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Validation of a new instrument to measure disease‐related distress among patients with haemophilia.
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- Haemophilia, 2021, v. 27, n. 1, p. 60, doi. 10.1111/hae.14187
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Occurrence rates of haemophilia among males in the United States based on surveillance conducted in specialized haemophilia treatment centres.
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- Haemophilia, 2020, v. 26, n. 3, p. 487, doi. 10.1111/hae.13998
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Improvements in Communication and Coordination of Care in a Hemophilia Treatment Center.
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- Acta Haematologica, 2021, v. 144, n. 6, p. 672, doi. 10.1159/000515350
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- Article