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Research 361–390 of 517
- 0975 Single-cell transcriptomic profiling reveals distinct immunopathogenic programs in alopecia totalis/universalis compared to patchy alopecia areata
- Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
- 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
- New Topical Treatment for Psoriasis
- “Degeneration” in Dermatopathology
- Co-Expression Pattern of Artemis Serine 516 Phosphorylation with Indicators Involving in Differentiation, Proliferation and Apoptosis of Human Anagen Hair Follicles: An Immunofluorescence Double-Staining Study
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- The skin as a window on internal disorders: Two cases of internal malignancy and hypervitaminosis B12
- Psoriasis Research: A Comprehensive Review
- Skin-infiltrating CD4+ lymphoma cells depend on hair follicle-derived IL-7
- Trichorrhexis Invaginata and Netherton’s Syndrome
- The Role of Vitamin D3 Deficiency and Colonization of the Oral Mucosa by Candida Yeast-like Fungi in the Pathomechanism of Psoriasis
- Emerging Topical and Systemic JAK Inhibitors in Dermatology
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Hair follicle–derived IL-7 and IL-15 mediate skin-resident memory T cell homeostasis and lymphoma
- The IL-23/IL-17 Pathway in Inflammatory Skin Diseases: From Bench to Bedside
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- The use of cyclosporine in dermatology: Part I
- Proteome Analysis of Human Hair Shaft
- Cutaneous manifestations and considerations in COVID ‐19 pandemic: A systematic review
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Hidradenitis suppurativa: A practical review of possible medical treatments based on over 350 hidradenitis patients
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- The molecular basis of human keratin disorders
- Rapidly progressing mycosis fungoides presenting as follicular mucinosis
- Trichoscopy in genetic hair shaft abnormalities