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Research 391–420 of 707
- Prospective Case Series of Cutaneous Adverse Effects Associated With Dabrafenib and Trametinib
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- A newborn presenting with congenital blistering
- 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
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- 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
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- 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
- 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
- Disorders of Keratinization
- 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
- A four generation hidrotic ectodermal dysplasia family: an allelic variant of Clouston syndrome?
- Dysfunction of keratinocyte adhesion
- P029 A case of atypical bullous pemphigoid
- PA05 A rare case of cardiocutaneous syndrome in a young child
- LB1671 Large-scale skin scRNA-seq profiling highlights distinct body site-specific ligand-receptor interactions and pathways in keratinocytes