Validation of medical service insurance claims as a surrogate for ascertaining vitiligo cases
Author:
Funder
Michael Smith Foundation for Health Research
Canadian Dermatology Foundation
Publisher
Springer Science and Business Media LLC
Subject
Dermatology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00403-022-02383-7.pdf
Reference28 articles.
1. Silverberg JI, Reja M, Silverberg NB (2014) Regional variation of and association of US Birthplace with vitiligo extent. JAMA Dermatol 150(12):1298–1305
2. Krüger C, Schallreuter KU (2012) A review of the worldwide prevalence of vitiligo in children/adolescents and adults. Int J Dermatol 51(10):1206–1212
3. Catucci BJ, Giongo N, Machado P, Horn R, Fabbrin A, Cestari T (2016) Quality of life impairment in children and adults with vitiligo: a cross-sectional study based on dermatology-specific and disease-specific quality of life instruments. Dermatology 232(5):619–625
4. Benchimol EI, Smeeth L, Guttmann A et al (2016) The reporting of studies conducted using observational routinely-collected health data (RECORD) statement. Z Evid Fortbild Qual Gesundhwes 1(115):33–48
5. Wehner MR, Levandoski KA, Kulldorff M, Asgari MM (2017) Research techniques made simple: an introduction to use and analysis of big data in dermatology. J Invest Dermatol 137(8):e153–e158
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