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Research 241–270 of 649
- 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
- Vitamins
- 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
- Phosphodiesterase (PDE) Inhibitors for the Treatment of Inflammatory Skin Conditions
- Disorders of Keratinization
- - Tumor necrosis factor-alpha inhibitor associated psoriasiform alopecia (drug-induced psoriasiform alopecia)
- Woolly Hair in Two Siblings
- Chemotherapy-induced dermatological toxicity: frequencies and impact on quality of life in women’s cancers. Results of a prospective study
- Treatment of Psoriasis vulgaris with a New Retinoic Acid Derivative Ro 10-9359
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- Dysfunction of keratinocyte adhesion
- P029 A case of atypical bullous pemphigoid