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Research 31–60 of 794
- Ichthyoses
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- New developments in the molecular treatment of ichthyosis: review of the literature
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- First Symposium of Ichthyosis Experts
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Oral Retinoids in Dermatology
- Chemotherapy of psoriasis and other skin disorders with oral retinoids
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Chronic Ulceration of the Scalp Associated with Genetically Different Types of Congenital Ichthyosis: A Series of Four Cases
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Hair follicles modulate skin barrier function
- Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism
- Disorders of Keratinization
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- The Fate of Epidermal Tight Junctions in the stratum corneum: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin Conditions
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus: Is nomenclature “porokeratotic adnexal ostial nevus” more appropriate?
- The role of Glucosylceramides in Keratinocyte Differentiation and Epidermal Barrier Function
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Sarcoidosis: Are there differences in your skin of color patients?
- TCF/Lef1-Mediated Control of Lipid Metabolism Regulates Skin Barrier Function