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Research 17
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Dyschromatosis Universalis Hereditaria: Report of a case and Review of the Literature
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Zebrafish Model of Hereditary Pigmentary Disorders
- A case of dyschromatosis universalis
- 0441 Systemic autoimmune comorbidity in alopecia totalis and universalis compared with patchy alopecia areata: A retrospective cohort study
- A practical guide for the treatment of dandruff and seborrheic dermatitis
- Characterizing hair loss in female patients with systemic lupus erythematosus (SLE)
- Experimental models to investigate the efficacy and bioequivalence of low dose topical corticoids
- Comparison of the efficacy and safety of a picosecond alexandrite laser and a Q-switched alexandrite laser for the treatment of freckles in Chinese patients
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Optic Nerve Atrophy and Hair Loss in a Young Man
- Issue Information ‐ TOC
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- DIETHYLPROPION
- ESCITALOPRAM