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Research 181–210 of 320
- The Genetics of Human Skin Disease
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Congenital atrichia with papular lesions
- Off-label uses of retinoids in dermatology
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Alopezien und Hypotrichosen im Kindesalter
- A Threefold Association Between Vitiligo and Alopecia Areata: Results from a Nationwide Case-control Observational Study
- Marie-unna hereditary hypotrichosis
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Risk of autoimmune thyroid diseases in individuals with alopecia areata: A nationwide case‐control study
- First Symposium of Ichthyosis Experts
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Exploring the Dermoscopic Patterns in Tuberous Sclerosis
- Alopecia Areata and Systemic Lupus Erythematosus: Insights From a Nationwide Case–Control Study
- Atrichia with papular lesions mimicking alopecia areata universalis
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- The Non-Cosmetic Dermatological Use of Botulinum Neurotoxin
- Linear trichoepithelioma on the neck of a 15-year-old girl
- Genetics
- 0163 Specific targeting of dermal papilla cells with Hhip-Cre
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Structural mechanism of TRPV3 channel inhibition by the plant‐derived coumarin osthole
- Activation of TRPV3 Inhibits Lipogenesis and Stimulates Production of Inflammatory Mediators in Human Sebocytes—A Putative Contributor to Dry Skin Dermatoses
- No Evidence That Human Papillomavirus Is Responsible for the Aggressive Nature of Recessive Dystrophic Epidermolysis Bullosa–Associated Squamous Cell Carcinoma