• <em>Staphylococcus aureus</em> bacteremia and infective endocarditis in a patient with epidermolytic hyperkeratosis: A case report
• A de novo variant in the keratin 1 gene (KRT1) in a Chinese shar-pei dog with severe congenital cornification disorder and non-epidermolytic ichthyosis
• A Review of Dupilumab-Induced Adverse Events to Dermatologists and the Potential Pathogenesis in the Treatment of Atopic Dermatitis
• Alitretinoin as a Treatment Modality for Ichthyosis in Women of Childbearing Age: A Case Series and Review of the Literature
• Assessing the Application of Large Language Models in Generating Dermatologic Patient Education Materials According to Reading Level: Qualitative Study
• Assessing the use of dupilumab in a pediatric patient with bullous congenital ichthyosiform erythroderma
• Association of bullous pemphigoid and Grover disease induced by immune checkpoint therapy
• Atypical epidermolytic palmoplantar keratoderma is a minimal phenotypic variant of epidermolytic ichthyosis: A new insight from ultrastructural findings
• Chanarin-Dorfman Syndrome (CDS): A Rare Lipid Metabolism Disorder
• Clinical and genetic findings in 13 Chinese children with keratinopathic ichthyosis
• Deep Phenotyping of Superficial Epidermolytic Ichthyosis due to a Recurrent Mutation in <em>KRT2</em>
• Dermatological Manifestations in Patients With Chronic Kidney Disease: A Review
• Diagnostic Pearls of Vulvar Epidermolytic Acanthoma: Case Report
• Epidermal nevi and epidermolytic hyperkeratosis: A review of cases, highlighting indications for biopsy and genetics referral
• Epidermolytic epidermal nevus on the genitalia caused by a mosaic KRT10 mutation
• Epidermolytic Hyperkeratosis
• Epidermolytic Hyperkeratosis
• Epidermolytic hyperkeratosis of the vulva: Case report and review of the literature
• Epidermolytic ichthyosis complicated by staphylococcal scalded skin syndrome in the newborn
• Epidermolytic Ichthyosis in a Neonate
• Expression of hornerin in skin lesions of atopic dermatitis and skin diseases
• First Case of Superficial Epidermolytic Ichthyosis Successfully Treated by Dupilumab
• Four cases of Chanarin-Dorfman syndrome presenting with different types of erythrokeratoderma
• Generalized blistering and erythroderma in a young girl
• Hereditary epidermolytic palmoplantar keratosis due to a novel desmoglein-1 mutation: A case report
• Heterozygous KRT10 missense variant in a Chihuahua with severe epidermolytic ichthyosis
• Inflammatory linear verrucous epidermal nevus (ILVEN) encompasses a spectrum of inflammatory mosaic disorders
• Interleukin-18 as a severity marker and novel potential therapeutic target for epidermolytic ichthyosis
• Kaposi Varicelliform Eruption
• Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
• Nevus Comedonicus with Epidermolytic Hyperkeratosis: A Case Report
• Nonsense mutations in KRT1 caused recessive epidermolytic palmoplantar keratoderma with knuckle pads
• Novel Compound Heterozygous Mutations of <em>TGM1</em> Gene Identified in a Turkish Collodion Baby Diagnosed with Non-Bullous Congenital Ichthyosiform Erythroderma
• Novel Compound Heterozygous Mutations of TGM1 Gene Identified in a Turkish Collodion Baby Diagnosed with Non-Bullous Congenital Ichthyosiform Erythroderma
• Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
• Oral verruciform hyperkeratotic lesions indicating the presence of plantar or palmoplantar keratodermas
• Transcriptomic response of peripheral blood mononuclear cells to secukinumab in epidermolytic ichthyosis
• Treating epidermolytic ichthyosis and ichthyosis with confetti with epidermal autografts cultured from revertant skin
• Two cases of KRT1 mutation-associated epidermolytic ichthyosis without typical epidermolytic hyperkeratosis in the neonatal skin lesions
• Variants in the L12 linker domain of KRT10 are causal to atypical epidermolytic ichthyosis