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Research 10 of 17

1. Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria Journal of Investigative Dermatology · 2013 · 99 citations
2. Dyschromatosis Universalis Hereditaria: Report of a case and Review of the Literature Pediatric Dermatology · 2002 · 59 citations
3. The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria 2022 · 2 citations
4. SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature Pigment Cell & Melanoma Research · 2025 · 1 citations
5. Zebrafish Model of Hereditary Pigmentary Disorders International Journal of Dermatology and Venereology · 2019 · 1 citations
6. A case of dyschromatosis universalis Journal of The American Academy of Dermatology · 2004
7. 0441 Systemic autoimmune comorbidity in alopecia totalis and universalis compared with patchy alopecia areata: A retrospective cohort study Journal of Investigative Dermatology · 2026
8. A practical guide for the treatment of dandruff and seborrheic dermatitis Journal of The American Academy of Dermatology · 2004 · 5 citations
9. Characterizing hair loss in female patients with systemic lupus erythematosus (SLE) Journal of The American Academy of Dermatology · 2004
10. Experimental models to investigate the efficacy and bioequivalence of low dose topical corticoids Journal of The American Academy of Dermatology · 2004

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