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Research 511–540 of 679
- 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
- Linear and Unilateral Basaloid Follicular Hamartoma Along Blaschko’s Lines in an Elderly Patient: A Rare Presentation
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- 54269 Patchy hair loss, hyperpigmented plaques, and hyperkeratotic papules in a middle aged woman
- 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
- A clinical study of Geriatric dermatoses at Tertiary care center in South 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.
- The therapeutic efficacy of mesenchymal stem cells and their extracellular vesicles in the treatment of diverse skin diseases
- JAK inhibitors in dermatology: The promise of a new drug class
- 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
- Cytochrome P450: A Target for Drug Development for Skin Diseases
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture