43 results on '"Husson, Olga"'
Search Results
2. Financial difficulties experienced by patients with gastrointestinal stromal tumours (GIST) in the Netherlands: data from a cross-sectional multicentre study
3. Protocol for the development of a Core Outcome Set (COS) for Adolescents and Young Adults (AYAs) with cancer
4. Exploring the interconnectedness between health-related quality of life factors among long-term adolescent and young adult cancer survivors (AYAs): a network analysis
5. The impact of electronic versus paper-based data capture on data collection logistics and on missing scores in thyroid cancer patients
6. A qualitative study on the healthcare experiences of adolescents and young adults (AYA) with an uncertain or poor cancer prognosis
7. Patient-physician agreement on function and pain is associated with long-term outcomes in sarcoma: findings from a longitudinal study
8. Health-related quality of life of Adolescent and Young Adult Cancer Survivors before and during the COVID-19 pandemic: longitudinal improvements on social functioning and fatigue
9. Determinants and mediating mechanisms of quality of life and disease-specific symptoms among thyroid cancer patients: the design of the WaTCh study
10. Psychological and social challenges of patients with locally advanced and metastatic gastrointestinal stromal tumours (GIST) on long-term treatment with tyrosine kinase inhibitors: a qualitative study with patients and medical oncologists
11. Assessing the collection and reporting of patient-reported outcome data in interventional cancer trials: a single institution, retrospective systematic evaluation
12. A qualitative study on the involvement of adolescents and young adults (AYAs) with cancer during multiple research phases: “plan, structure, and discuss”
13. Identifying health-related quality of life cut-off scores that indicate the need for supportive care in young adults with cancer
14. ‘I thought I had fibroids, and now I don’t’: a mixed method study on health-related quality of life in uterine sarcoma patients
15. Symptoms reported by gastrointestinal stromal tumour (GIST) patients on imatinib treatment: combining questionnaire and forum data
16. Assessing measurement invariance in the EORTC QLQ-C30
17. Self-perceived cognitive functioning and quality of life among cancer survivors: results from the PROFILES registry
18. Self-reported causes of cancer among 6881 survivors with 6 tumour types: results from the PROFILES registry
19. The complexity of assessing health-related quality of life among sarcoma patients
20. Evaluating a digital tool for supporting breast cancer patients: a randomized controlled trial protocol (ADAPT)
21. Assessing health-related quality of life in cancer survivors: factors impacting on EORTC QLU-C10D-derived utility values
22. Outcome of Primary Desmoid Tumors at All Anatomic Locations Initially Managed with Active Surveillance
23. An immunotherapy survivor population: health-related quality of life and toxicity in patients with metastatic melanoma treated with immune checkpoint inhibitors
24. Psychometric properties of the 45-item supportive care needs survey—partners and caregivers - Dutch (SCNS-P&C45-D) in partners of patients with breast cancer
25. Presence of gastro-intestinal symptoms in ovarian cancer patients during survivorship: a cross-sectional study from the PROFILES registry
26. Age-related sarcoma patient experience: results from a national survey in England
27. Cancer survivors not participating in observational patient-reported outcome studies have a lower survival compared to participants: the population-based PROFILES registry
28. Desmoid fibromatosis through the patients’ eyes: time to change the focus and organisation of care?
29. Identification and assessment of health-related quality of life issues in patients with sporadic desmoid-type fibromatosis: a literature review and focus group study
30. Prevalence and correlates of high fear of cancer recurrence in late adolescents and young adults consulting a specialist adolescent and young adult (AYA) cancer service
31. Identifying the subtypes of cancer-related fatigue: results from the population-based PROFILES registry
32. Erratum to: Prevalence and impact of severe fatigue in adolescent and young adult cancer patients in comparison with population-based controls
33. Prevalence and impact of severe fatigue in adolescent and young adult cancer patients in comparison with population-based controls
34. Lymphoma InterVEntion (LIVE) – patient-reported outcome feedback and a web-based self-management intervention for patients with lymphoma: study protocol for a randomised controlled trial
35. The development and validation of the Leiden Bother and Needs Questionnaire for patients with pituitary disease: the LBNQ-Pituitary
36. Correlates of physical activity among colorectal cancer survivors: results from the longitudinal population-based profiles registry
37. The course of fatigue and its correlates in colorectal cancer survivors: a prospective cohort study of the PROFILES registry
38. Chemotherapy-induced peripheral neuropathy, physical activity and health-related quality of life among colorectal cancer survivors from the PROFILES registry
39. Health-related quality of life is associated with physical activity levels among colorectal cancer survivors: a longitudinal, 3-year study of the PROFILES registry
40. Variation in fatigue among 6011 (long-term) cancer survivors and a normative population: a study from the population-based PROFILES registry
41. Depressive symptoms are a risk factor for all-cause mortality: results from a prospective population-based study among 3,080 cancer survivors from the PROFILES registry
42. Perceived information provision and satisfaction among lymphoma and multiple myeloma survivors—results from a Dutch population-based study
43. The impact of a cancer Survivorship Care Plan on gynecological cancer patient and health care provider reported outcomes (ROGY Care): study protocol for a pragmatic cluster randomized controlled trial
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