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Research 211–240 of 693
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- First Symposium of Ichthyosis Experts
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Two Clinically Unusual Cases of Folliculotropic Mycosis Fungoides: One with and the Other without Syringotropism
- Substance P in keratosis follicularis spinulosa decalvans
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- The epidermis: rising to the surface
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- The molecular basis of human keratin disorders
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Genetic hair and nail disorders
- Activation of TRPV3 Inhibits Lipogenesis and Stimulates Production of Inflammatory Mediators in Human Sebocytes—A Putative Contributor to Dry Skin Dermatoses
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- Erythroderma, Alopecia, Anhidrosis, and Vitiligo as Complications of a Red Ink Tattoo—A Case Report
- Review of Promising Off-Label Use of Deucravacitinib
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- “Degeneration” in Dermatopathology
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Immunofluorescent findings and clinical overlap in two cases of follicular lichen planus
- Folliculotropic CD8+ mycosis fungoides associated with diffuse mucosal involvement
- Molecular Genetics of Human Hair Diseases
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology