Economic burden and quality of life of caregivers of patients with sickle cell disease in the United Kingdom and France: a cross-sectional study.
- DOI
- 10.1186/s41687-024-00784-y
- Published
- 2024 Sep 26
- Container
- Journal of patient-reported outcomes
- Publisher
- Not recorded
- Open access
- yes
Credibility signals
limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.1186/s41687-024-00784-y,
title = {Economic burden and quality of life of caregivers of patients with sickle cell disease in the United Kingdom and France: a cross-sectional study.},
author = {Besser M and O'Sullivan SB and Bourke S and Longworth L and Barcelos GT and Oluboyede Y},
year = {2024},
journal = {Journal of patient-reported outcomes},
doi = {10.1186/s41687-024-00784-y},
url = {https://doi.org/10.1186/s41687-024-00784-y}
}RIS
TY - JOUR TI - Economic burden and quality of life of caregivers of patients with sickle cell disease in the United Kingdom and France: a cross-sectional study. AU - Besser M AU - O'Sullivan SB AU - Bourke S AU - Longworth L AU - Barcelos GT AU - Oluboyede Y PY - 2024 JO - Journal of patient-reported outcomes DO - 10.1186/s41687-024-00784-y UR - https://doi.org/10.1186/s41687-024-00784-y ER -
APA
M, B., SB, O., S, B., L, L., GT, B., & Y, O. (2024). Economic burden and quality of life of caregivers of patients with sickle cell disease in the United Kingdom and France: a cross-sectional study.. Journal of patient-reported outcomes. https://doi.org/10.1186/s41687-024-00784-y
Source records
- pubmed · retrieved 2026-09-25T11:15:09.312Z