• 3D-Organotypic Cultures to Unravel Molecular and Cellular Abnormalities in Atopic Dermatitis and Ichthyosis Vulgaris
• 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
• A rare case of acute intermittent porphyria with ichthyosis vulgaris in a young boy
• A unique case of a digital tourniquet in ichthyosis vulgaris
• Acquired Ichthyosis in the Setting of Active Pulmonary Tuberculosis
• Acquired ichthyosis, asteatotic dermatitis or xerosis? An update on pathoetiology and drug-induced associations
• Acral Melanoma in an Elderly Patient with Congenital Ichthyosis Vulgaris
• Alterations in mental health and quality of life in patients with skin disorders: a narrative review
• Assessing the Application of Large Language Models in Generating Dermatologic Patient Education Materials According to Reading Level: Qualitative Study
• Asthma severity, nature or nurture: genetic determinants
• Basket-weave structure in the stratum corneum is an important factor for maintaining the physiological properties of human skin as studied using reconstructed human epidermis and tape stripping of human cheek skin
• 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
• Clinical examination for hyperlinear palms to determine filaggrin genotype: A diagnostic test accuracy study
• Clinico-Epidemiologic Profile of Non-Syndromic Congenital Ichthyosis - A Retrospective Chart Review of 107 Patients
• Clinico-epidemiological Study of Congenital Ichthyosis in a Tertiary Care Center of Eastern India
• Co-occurrence of Ichthyosis Vulgaris, Dowling-Degos Disease, and Hidradenitis Suppuritiva in Same Patient: An Association or Coincidence?
• Coexistence of palmoplantar pustulosis and ichthyosis vulgaris treated by risankizumab
• Concurrent Chondrodysplasia Punctata Type 2 (Conradi-Hunermann-Happle Syndrome) and Ichthyosis Vulgaris in Teenaged Twin Girls
• CRISPR-Cas9‒Based Genomic Engineering in Keratinocytes: From Technology to Application
• Current and emerging concepts in atopic dermatitis pathogenesis
• Cutaneous Melanoma in Association With Ichthyosis Vulgaris
• Dermatological aspects of the S2k guidelines on Down syndrome in childhood and adolescence
• Dermatologische Aspekte aus der S2k-Leitlinie zum Down-Syndrom im Kindes- und Jugendalter
• Disseminated tinea incognita in a patient with ichthyosis vulgaris and eczema
• 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
• Embryonic AP1 Transcription Factor Deficiency Causes a Collodion Baby-Like Phenotype
• Enhanced Expression of Genes Related to Xenobiotic Metabolism in the Skin of Patients with Atopic Dermatitis but Not with Ichthyosis Vulgaris
• Exacerbation of ichthyosis vulgaris phenotype by co-inheritance of STS and FLG mutations in a Chinese family with ichthyosis: a case report
• Eyelash length for the diagnosis of atopic dermatitis and ichthyosis vulgaris in children-a case control study
• Eyelash trichomegaly: a systematic review of acquired and congenital aetiologies of lengthened lashes
• Filaggrin and atopic march
• Filaggrin expression via immunohistochemistry in basal cell carcinoma and squamous cell carcinoma
• Filaggrin gene polymorphisms in Iranian ichthyosis vulgaris and atopic dermatitis patients
• 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
• Formation of keto-type ceramides in palmoplantar keratoderma based on biallelic KDSR mutations in patients
• Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia-Alania, Case Series Report
• Genetics of Inherited Ichthyoses and Related Diseases
• Genodermatoses in Las Tunas Province, Cuba, 1989-2019
• Genotype Study of Filaggrin Gene Loss-of-Function Mutations in Central India Population with Atopic Dermatitis and Ichthyosis Vulgaris
• Grover's Disease in a Kidney Transplant Recipient
• Grover's disease in a patient with pemphigus vulgaris
• Hereditary and Acquired Ichthyosis Vulgaris
• Hereditary and Acquired Ichthyosis Vulgaris
• Ichthyoses in everyday practice: management of a rare group of diseases
• Ichthyosis Skin Changes in a Patient With Hereditary Hemochromatosis
• Ichthyosis vulgaris
• Ichthyosis vulgaris: a pedigree with 13 cases
• Ichthyosis vulgaris: An updated review
• Immunohistochemical evaluation of epidermal proliferation, differentiation and melanocytic density in symmetrical acrokeratoderma
• Initial Evidence of Distinguishable Bacterial and Fungal Dysbiosis in the Skin of Patients with Atopic Dermatitis or Netherton Syndrome
• Investigations into the FLG Null Phenotype: Showcasing the Methodology for CRISPR/Cas9 Editing of Human Keratinocytes
• Kaposi Varicelliform Eruption
• Kaposi Varicelliform Eruption
• Keratosis Pilaris
• Keratosis Pilaris
• Keratosis pilaris: an update and approach to management
• L-Histidine for Treatment of Ichthyosis Vulgaris
• Low Threshold for Cutaneous Allergen Sensitization but No Spontaneous Dermatitis or Atopy in FLG-Deficient Mice
• Memory, mood and associated neuroanatomy in individuals with steroid sulphatase deficiency (X-linked ichthyosis)
• Mindfulness-Based Cognitive Hypnotherapy and Skin Disorders
• Mood symptoms, neurodevelopmental traits, and their contributory factors in X-linked ichthyosis, ichthyosis vulgaris and psoriasis
• 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
• Next-generation sequencing through multi-gene panel testing for diagnosis of hereditary ichthyosis in Chinese
• Novel Homozygous Mutations in the Genes <em>TGM1</em>, <em>SULT2B1</em>, <em>SPINK5</em> and <em>FLG</em> in Four Families Underlying Congenital Ichthyosis
• Novel Homozygous Mutations in the Genes TGM1, SULT2B1, SPINK5 and FLG in Four Families Underlying Congenital Ichthyosis
• Palmar hyperlinearity in early childhood atopic dermatitis is associated with filaggrin mutation and sensitization to egg
• Paraneoplastic skin diseases
• Pigmented transverse nasal band: A distinct presentation
• Red-brown patches in the groin
• Revisiting the Roles of Filaggrin in Atopic Dermatitis
• Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families
• Skin diseases associated with atopic dermatitis
• Spectrum of ichthyoses in an Austrian ichthyosis cohort from 2004 to 2017
• Spektrum der Ichthyosen in einer österreichischen Ichthyosekohorte von 2004-2007
• Steroid sulfatase and filaggrin mutations in a boy with severe ichthyosis, elevated serum IgE level and moyamoya syndrome
• Surgical management of digital ischemia caused by constriction band formation in a patient with ichthyosis vulgaris
• The Discovery and Function of Filaggrin
• The Potential Uses of N-acetylcysteine in Dermatology: A Review
• Topical urea in skincare: A review
• Treatment of ichthyosis vulgaris with a urea-based emulsion: videodermatoscopy and confocal microscopy evaluation
• Trifarotene: A Current Review and Perspectives in Dermatology
• Uncrossed corticospinal tracts in a patient with ichthyosis and hemiparesis: a case report
• Unique variants in the <em>FLG</em> gene and <em>FERMT1</em> gene in a Chinese patient with ichthyosis and Kindler syndrome
• Unique variants in the FLG gene and FERMT1 gene in a Chinese patient with ichthyosis and Kindler syndrome
• Utilization of patterned bioprinting for heterogeneous and physiologically representative reconstructed epidermal skin models
• Validity of First-Time Diagnoses of Inherited Ichthyosis in the Danish National Patient Registry and the Danish Pathology Registry
• Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling
• Whole exome sequencing identified two point mutations of COL7A1 and FLG in a Chinese family with dystrophic epidermolysis bullous pruriginosa and ichthyosis vulgaris
• X-linked and autosomal dominant forms of the ichthyosis in coinheritance
• X-Linked Ichthyosis
• X-linked ichthyosis: Clinical and molecular findings in 35 Italian patients