Quality of life remains poor for patients with pemphigus vulgaris despite targeted therapies

B. Schultz, E. Latour, N. Fett

Research output: Contribution to journalLetterpeer-review

5 Scopus citations
Original languageEnglish (US)
Pages (from-to)1101-1103
Number of pages3
JournalBritish Journal of Dermatology
Issue number5
StatePublished - Nov 1 2019

Bibliographical note

Funding Information:
The authors are indebted to Becky Strong and the International Pemphigoid and Pemphigus Foundation for their assistance in this project as well as the Medical Dermatology Society for awarding Brittney Schultz a mentorship with Nicole Fett to complete this research. We also thank the authors of the Autoimmune Bullous Disease Quality of Life and Treatment of Autoimmune Bullous Disease Quality of Life for sharing the questionnaires.

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