Using qualitative methods to establish the clinically meaningful threshold for treatment success in alopecia areata
Author:
Funder
Eli Lilly and Company
Publisher
Springer Science and Business Media LLC
Subject
Public Health, Environmental and Occupational Health
Link
https://link.springer.com/content/pdf/10.1007/s11136-022-03170-7.pdf
Reference33 articles.
1. Liu, L. Y., King, B. A., & Craiglow, B. G. (2016). Health-related quality of life (HRQoL) among patients with alopecia areata (AA): A systematic review. Journal of the American Academy of Dermatology, 75(4), 806–12.e3.
2. Rencz, F., Gulácsi, L., Péntek, M., Wikonkál, N., Baji, P., & Brodszky, V. (2016). Alopecia areata and health-related quality of life: A systematic review and meta-analysis. British Journal of Dermatology, 175(3), 561–571.
3. Davis, D. S., & Callender, V. D. (2018). Review of quality of life studies in women with alopecia. International Journal of Women’s Dermatology, 4(1), 18–22.
4. Wolf, J. J., & Hudson, B. P. (2019). Alopecia areata: Factors that impact children and adolescents. Journal of Adolescent Research., 34(3), 282–301.
5. Davey, L., Clarke, V., & Jenkinson, E. (2019). Living with alopecia areata: An online qualitative survey study. British Journal of Dermatology., 180(6), 1377–1389.
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