• A case of erythema ab igne with histopathological features resembling keratosis lichenoides chronica
• A Case of Ichthyosis Vulgaris and the Use of 70% Glycolic Acid Chemical Peels for Management
• A Cross-Sectional Study Comparing Application of Hanifin and Rajka Criteria in Indian Pediatric Atopic Dermatitis Patients to that of Other Countries
• A novel combination of mutations leading to congenital ichthyosis and ichthyosis vulgaris
• Acquired ichthyosis, asteatotic dermatitis or xerosis? An update on pathoetiology and drug-induced associations
• Acral Melanoma in an Elderly Patient with Congenital Ichthyosis Vulgaris
• Assessing the Application of Large Language Models in Generating Dermatologic Patient Education Materials According to Reading Level: Qualitative Study
• Biallelic mutations in FLG, TGM1, and STS genes segregated with different types of ichthyoses in eight families of Pakistani origin
• Charcot-Marie-Tooth Disease Type 4C and Autosomal Dominant Heterozygous Ichthyosis Vulgaris, with Bilateral Hearing Loss: A Novel Association with Review of Literature
• Chronic diarrhoea and ichthyosis vulgaris: a rare presentation of Hodgkin's lymphoma
• Clinico-Epidemiologic Profile of Non-Syndromic Congenital Ichthyosis - A Retrospective Chart Review of 107 Patients
• Dual clinical features of fine and rough scales seen in a combined ichthyosis vulgaris and X-linked recessive ichthyosis patient with atopic dermatitis
• Effect of topical treatment with 7.5% urea in Ichthyosis Vulgaris: A randomized, controlled, double blinded, split body study evaluating the effect of urea cream compared to the vehicle (moisturizing) cream
• Filaggrin gene variants among Saudi patients with ichthyosis vulgaris
• Filaggrin-Associated Atopic Skin, Eye, Airways, and Gut Disease, Modifying the Presentation of X-Linked Reticular Pigmentary Disorder (XLPDR)
• FLG Deficiency in Mice Alters the Early-Life CD4⁺ T-Cell Response to Skin Commensal Bacteria
• Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia-Alania, Case Series Report
• Genotype Study of Filaggrin Gene Loss-of-Function Mutations in Central India Population with Atopic Dermatitis and Ichthyosis Vulgaris
• Hereditary and Acquired Ichthyosis Vulgaris
• Hereditary and Acquired Ichthyosis Vulgaris
• Ichthyosis Skin Changes in a Patient With Hereditary Hemochromatosis
• Ichthyosis vulgaris: An updated review
• Investigations into the FLG Null Phenotype: Showcasing the Methodology for CRISPR/Cas9 Editing of Human Keratinocytes
• Kaposi Varicelliform Eruption
• Keratosis Pilaris
• Keratosis Pilaris
• Keratosis pilaris: an update and approach to management
• Memory, mood and associated neuroanatomy in individuals with steroid sulphatase deficiency (X-linked ichthyosis)
• Nanopore sequencing enables allelic phasing of FLG loss-of-function variants, intragenic copy number variation and methylation status in atopic dermatitis and ichthyosis vulgaris
• Nanopore Sequencing Enables Allelic Phasing of FLG Loss-of-Function Variants, Intragenic Copy Number Variation, and Methylation Status in Atopic Dermatitis and Ichthyosis Vulgaris
• Revisiting the Roles of Filaggrin in Atopic Dermatitis
• X-Linked Ichthyosis