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Research 391–420 of 1000+
- What causes acne inversa (or hidradenitis suppurativa)? – the debate continues
- An Update on Medical Treatment Options for Hidradenitis Suppurativa
- Inactivity of Hidradenitis Suppurativa After Renal Transplantation
- Update on hidradenitis suppurativa: connecting the tracts
- Trichomycosis (trichobacteriosis) axillaris
- Congenital atrichia with papular lesions
- Werner's syndrome: incidental finding during pregnancy
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- Graham-Little Piccardi Lassueur Syndrome and review of the literature
- Eruptive vellus hair cyst: Treatment with topical tretinoin 0.025% cream
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Hirsutism, Normal Androgens and Diagnosis of PCOS
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- The Role of Sex and Gender in Dermatology - From Pathogenesis to Clinical Implications
- Acute generalized exanthematous pustulosis induced by hydroxychloroquine prescribed for COVID-19
- A Comprehensive Review of Acne Vulgaris
- Medical aesthetics – Current trends and a review of its applications
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Madarosis from mitochondriopathy
- Overexpression of hypoxia-inducible factor-1α in hidradenitis suppurativa: the link between deviated immunity and metabolism
- Microneedling: A means of collagen induction therapy
- Viewpoint 6
- Proceedings of the Joint CHSF/HSF/EHSF pre‐WCD Hidradenitis Suppurativa Symposium
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Hormonal Effects on Hair Follicles
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Intense Pulsed Light: From the Past to the Future