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Research 241–270 of 313
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Lrig1 Expression in Human Sebaceous Gland Tumors
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Zebrafish Model of Hereditary Pigmentary Disorders
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Hypothesis: platelet-rich plasma as an adjunct therapy for eczema targeting inflammation, skin barrier repair, and chronic recurrence
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Melanocytes in regenerative medicine applications and disease modeling
- Giant solitary trichoepithelioma: A rare trichogenic tumor
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Minoxidil oral en alopecias no androgénicas
- Alopecias: Practical Tips for the Management of Biopsies and Main Diagnostic Clues for General Pathologists and Dermatopathologists
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Use of Contact Immunotherapy in the Treatment of Skin Diseases Other than Alopecia Areata
- Subject Index
- Cell death by cornification
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Genetics of Inherited Ichthyoses and Related Diseases
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Primary cicatricial alopecia: diagnosis and treatment
- Therapeutic potential of bimatoprost for the treatment of eyebrow hypotrichosis