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Research 481–510 of 1000+
- 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.
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Alopecia and Associated Toxic Agents: A Systematic Review
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Trichoscopy in genetic hair shaft abnormalities
- Bimatoprost in the treatment of eyelash hypotrichosis
- The nude gene and the skin
- Syphilitic alopecia: uncommon trichoscopic findings
- “‘You lose your hair, what’s the big deal?’ I was so embarrassed, I was so self-conscious, I was so depressed:” a qualitative interview study to understand the psychosocial burden of alopecia areata
- Eyelash Transplantation Using Leg Hair by Follicular Unit Extraction
- A case of extensive alopecia areata following Pfizer‐BioNTech BNT162b2 mRNA COVID‐19 vaccine with favorable outcome
- Trichotillomania as a Manifestation of Dementia
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Permanent chemotherapy-induced alopecia after hematopoietic stem cell transplantation treated with low-dose oral minoxidil
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Trichoscopy pattern in alopecia areata: A systematic review and meta‐analysis
- Beard Alopecia: An Updated and Comprehensive Review of Etiologies, Presentation and Treatment
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Cronkhite-Canada syndrome: A case report and literature review
- Animals in Dermatology
- Hair Disorders in Autoimmune Diseases
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- Trichotillomania with Giant Gastric Trichobezoar in a Female Child: A Case Report
- TRICHOTILLOMANIA WITH GIANT GASTRIC TRICHOBEZOAR IN A FEMALE CHILD: A CASE REPORT
- Congenital triangular alopecia - A case report
- Dermoscopic Findings of Alopecia in Patients with Hypothyroidism
- Long‐hair follicular unit excision enhances the cosmetic results of hairline restoration: A retrospective study in Chinese recipients