N. Horevoorts

发表

Cancer survivors who fully participate in the PROFILES registry have better health-related quality of life than those who drop out

L. V. van de Poll-Franse, F. Mols, N. Corsini, 2019, Journal of Cancer Survivorship.

Reference data of the EORTC QLQ-C30 questionnaire: five consecutive annual assessments of approximately 2000 representative Dutch men and women

L. V. van de Poll-Franse, F. Mols, O. Husson, 2018, Acta oncologica.

Response Rates for Patient-Reported Outcomes Using Web-Based Versus Paper Questionnaires: Comparison of Two Invitational Methods in Older Colorectal Cancer Patients

L. V. van de Poll-Franse, F. Mols, N. Horevoorts, 2015, Journal of medical Internet research.

OP-JNCI220047 800..807

G. Hageman, S. Beijer, F. Mols, 2022 .

Perceived Care and Well-being of Patients With Cancer and Matched Norm Participants in the COVID-19 Crisis: Results of a Survey of Participants in the Dutch PROFILES Registry.

S. Siesling, S. Beijer, M. Koopman, 2020, JAMA oncology.

Financial toxicity is more than costs of care: the relationship between employment and financial toxicity in long-term cancer survivors

L. V. van de Poll-Franse, F. Mols, B. Koczwara, 2018, Journal of Cancer Survivorship.

Towards OPtimal TIming and Method for promoting sUstained adherence to lifestyle and body weight recommendations in postMenopausal breast cancer survivors (the OPTIMUM-study): protocol for a longitudinal mixed-method study

M. D. de Boer, J. Seidell, S. Beijer, 2021, BMC Women's Health.

“Am I normal?” The Wishes of Patients With Lymphoma to Compare Their Patient-Reported Outcomes With Those of Their Peers

L. V. van de Poll-Franse, S. Oerlemans, L. Arts, 2017, Journal of medical Internet research.

Cancer survivors not participating in observational patient-reported outcome studies have a lower survival compared to participants: the population-based PROFILES registry

L. V. van de Poll-Franse, F. Mols, S. Oerlemans, 2018, Quality of Life Research.

Measuring Clinical, Biological, and Behavioral Variables to Elucidate Trajectories of Patient-Reported Outcomes: The PROFILES Registry

G. Hageman, S. Beijer, L. V. van de Poll-Franse, 2022, Journal of the National Cancer Institute.

The Patient Reported Outcomes Following Initial treatment and Long term Evaluation of Survivorship registry: scope, rationale and design of an infrastructure for the study of physical and psychosocial outcomes in cancer survivorship cohorts.

J. Coebergh, J. Denollet, N. Aaronson, 2011, European journal of cancer.

Adjustment disorder in cancer patients after treatment: prevalence and acceptance of psychological treatment

I. V. Verdonck‐de Leeuw, F. Jansen, S. Eerenstein, 2021, Supportive Care in Cancer.

Response Rates for Patient-Reported Outcomes Using Web-Based Versus Paper Questionnaires: Comparison of Two Invitational Methods in Older Colorectal Cancer Patients

L. V. van de Poll-Franse, F. Mols, N. Horevoorts, 2015, Journal of medical Internet research.