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Research 481–510 of 650
- Systemic retinoids and thyrotoxicosis in (Multi) nodular goiter: Side effect or coincidence?
- Validation of <i>International Classification of Diseases</i> Codes for Dermatologic Conditions
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- S4890 Infliximab-Induced Synovitis, Acne, Pustulosis, Hyperostosis, Osteitis Syndrome
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- DP15 Syphilis: the chameleon disease. A case series of unexpected mimicry
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- 151 High effectiveness of tildrakizumab over 52 weeks in patients with or without nail psoriasis: results from the phase IV POSITIVE Austrian subset
- 272 Dupilumab treatment in children with alopecia areata: A real-world, single-center observational study
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Cutaneous manifestations of hypothyroidism: An observational study in a tertiary care center of Eastern India
- “Degeneration” in Dermatopathology
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Painful thickened skin on the soles of the feet
- Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Pioneers in Dermatology and Venereology: An Interview with Professor Danilo V. Stevanovic
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- Fibroblasts: Origins, definitions, and functions in health and disease
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Expression of Hypothalamic–Pituitary–Thyroid Axis RelatedGenes in the Human Skin
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- TRP Channels in Skin Biology and Pathophysiology
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype