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Research 61–90 of 670
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- A newborn presenting with congenital blistering
- Challenging Regional Psoriasis and Ustekinumab Biotherapy: Impact of the Patterns of Disease
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Building Models for Keratin Disorders
- Follicular cysts and hyperkeratoses in early mycosis fungoides
- Olmsted syndrome
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Vitamins
- Editorial: Exploring innovative therapies for rare inflammatory skin diseases
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Evolving treatment paradigms in dermatology: Insights from emerging and repurposed therapies
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Ectodermal Dysplasia: Variable Expressions
- Surgical Management of Severe Cicatricial Ectropion Secondary to Pityriasis Rubra Pilaris.
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Successful Treatment of Adalimumab-Induced Paradoxical Skin Reactions in Pustulotic Arthro-Osteitis With Guselkumab
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- 394 Differential associations of psoriasis subtypes with autoimmune disorders in United States children and adults: A cross-sectional study
- IL-17 axis is a significant driver of skin inflammation in Card14 mutant pityriasis rubra pilaris model mice
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- GC-TOF/MS-Based Metabolomics for Comparison of Volar and Non-Volar Skin Types
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- Clouston’s Syndrome-A Case Report
- Clouston’s syndrome: a rare case report
- KRT16 wt Allele
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- Cirmcumscribed juvenile pityriasis rubra pilaris in a 5-year-old-girl treated with topical keratolytic and steroid
- Phosphodiesterase (PDE) Inhibitors for the Treatment of Inflammatory Skin Conditions