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Research 751–780 of 1000+
- Visualising Androgen Receptor Activity in Male and Female Mice
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Development of Heritable Melanoma in Transgenic Mice
- Trichoscopy in genetic hair shaft abnormalities
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Multi-layered environmental regulation on the homeostasis of stem cells: The saga of hair growth and alopecia
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Cosmetic Treatment Using Botulinum Toxin in the Oral and Maxillofacial Area: A Narrative Review of Esthetic Techniques
- Swiss Practice Recommendations for the Management of Hidradenitis Suppurativa/Acne Inversa
- Madarosis: A marker of many Maladies
- Black women’s hair: the main scalp dermatoses and aesthetic practices in women of African ethnicity
- Genetic Hair Disorders: A Review
- HAIR LOSS AND REGENERATION PERFORMED ON ANIMAL MODELS
- Two Clinically Unusual Cases of Folliculotropic Mycosis Fungoides: One with and the Other without Syringotropism
- Lichen planopilaris and frontal fibrosing alopecia: review and update of diagnostic and therapeutic features
- Establishment of type II 5α-reductase over-expressing cell line as an inhibitor screening model
- Molecular Basis of Androgenetic Alopecia
- Clinical and histopathological characteristics in patients with scarring folliculitis type of acne inversa
- Alopecia areata as a paraneoplastic syndrome of Hodgkin’s lymphoma: A case report
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Game Changers: Blockbuster Small-Molecule Drugs Approved by the FDA in 2024
- Alopecia areata after mogamulizumab treatment
- Clinical recognition and management of alopecia in women of color,
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Adolescent acne: association to sex, puberty, testosterone and dihydrotestosterone
- Hidradenitis Suppurativa Tunnels: Unveiling a Unique Disease Entity
- Differentiation of frontal fibrosing alopecia and Lichen planopilaris on trichoscopy: A comprehensive review
- Epstein-Barr virus associated with high-grade B-cell lymphoma in nude severe combined immunodeficiency