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Research 241–270 of 1000+
- Chikungunya virus infection in the skin: histopathology and cutaneous immunological response
- Wnt signaling in skin organogenesis
- Diseases of Periocular Hair
- Biotinidase deficiency characterized by skin and hair findings
- The Role of Histone Demethylases in Disease
- Metabolic pathways of eicosanoids—derivatives of arachidonic acid and their significance in skin
- Dermoscopy — 4th Conference of the Section of Dermoscopy and Other Skin Imaging Techniques (DiTOS) of the Polish Dermatological Society — Abstracts
- Peripheral blood gene expression in alopecia areata reveals molecular pathways distinguishing heritability, disease and severity
- The keratins and their disorders
- Comparative dermatology—canine endocrine dermatoses
- The Use of Human Dermal Papillae Conditioned Medium (HDPCM) on Aplasia Cutis Congenita in Lower Extremity due to Intrauterine Varicella Infection
- Dermatologic manifestations of endocrine disorders
- Congenital Adrenal Hyperplasia
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Exploring Pediatric Dermatology in Skin of Color: Focus on Dermoscopy
- Sebaceous gland diseases: clinical picture risk factors and treatment
- Keratin disorders: from gene to therapy
- Adverse Reactions to Oral Retinoids An Update
- SWEET SYNDROME: AN UNUSUAL PRESENTATION OF CHRONIC GRANULOMATOUS DISEASE IN A CHILD
- Dermatologic manifestations of endocrine disorders
- T-Cell Reconstitution after Thymus Xenotransplantation Induces Hair Depigmentation and Loss
- Murine Epidermal Ceramide Synthase 4 Is a Key Regulator of Skin Barrier Homeostasis
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
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- Phylloid terminal hair nevus: A unique clinical entity
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Dermatoses of pregnancy