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Research 421–450 of 1000+
- Oral cyclosporin does not arrest progression of androgenetic alopecia
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Facial hair enhancement with minoxidil—an off-label use
- The efficacy of topical prostaglandin analogs for hair loss: A systematic review and meta-analysis
- Combination Treatment with Methotrexate for Severe Alopecia Areata
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Poliosis circumscripta: Overview and underlying causes
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Efficacy and safety of botulinum toxin A in the treatment of female pattern hair loss
- Eyelash Trichomegaly: A Rare Presenting Feature of Systemic Lupus Erythematosus.
- Application of Topical Immunotherapy in the Treatment of Alopecia Areata: A Review and Update
- Novel treatment of female-pattern androgenetic alopecia with injected bimatoprost 0.03% solution.
- Prostaglandin F2α stimulates the growth of human intermediate hair follicles in ex vivo organ culture with potential clinical relevance
- Prostaglandin analogs for hair growth: Great Expectations
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Immunostaining study of cytokeratins in human hair follicle development
- 52993 Regulatory γδ T cells protect human scalp hair follicles from alopecia areata in vivo
- 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.
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Value of dermoscopy for the diagnosis of monilethrix
- Treatment of Alopecia in Children
- Discreet monilethrix: De novo mutation on the example of polish families
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Bilateral Xen is Used as Minimally Invasive Glaucoma Surgery for Glaucoma in GAPO Syndrome: Case Report
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- British Association of Dermatologists living guideline for managing people with alopecia areata 2024
- Ruxolitinib found to cause eyelash growth: a case report
- British Association of Dermatologists living guideline for managing people with alopecia areata 2025
- The Frontal Fibrosing Alopecia Treatment Dilemma