Developing a minimum data set required to create a registry system for patients with vitiligo

BACKGROUND: Vitiligo can be psychologically devastating and stigmatizing, with significant impacts on patients. As such, the early treatment and understanding of the profound psychosocial impact of this skin disease cannot be overstated. A standardized method of data collection with consistent defin...

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Detalles Bibliográficos
Autores principales: Arabkermani, Zahra, Sheikhtaheri, Abbas, Aryanian, Zeinab, Bastani, Peivand, Esmaeli, Nafiseh, Bashiri, Azadeh, Mehralian, Gholamhossein, Sharifian, Roxana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812701/
https://www.ncbi.nlm.nih.gov/pubmed/36619402
http://dx.doi.org/10.1016/j.heliyon.2022.e12641

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812701/
https://www.ncbi.nlm.nih.gov/pubmed/36619402
http://dx.doi.org/10.1016/j.heliyon.2022.e12641

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