Search
for
Sort by
Research 781–810 of 803
- Acne Vulgaris
- Proceedings of the Inaugural Pediatric Dermatology Research Alliance (PeDRA) Conference
- Oral Presentations
- Subject Index
- Subject Index
- Molecular Genetics of Human Hair Diseases
- TONGUE, RED
- NEFAZODONE
- Acanthosis nigricans, insulin resistance and cutaneous virilism
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Skin Structure, Physiology, and Pathology in Topical and Transdermal Drug Delivery
- Suppression of Vitamin D Receptor and Induction of Retinoid X Receptor α Expression During Squamous Differentiation of Cultured Keratinocytes
- Common Skin Diseases and Their Psychosocial Impact among Jazan Population, Saudi Arabia: A Cross-Sectional Survey during 2023
- Acetyl-CoA synthesis in the skin is a key determinant of systemic lipid homeostasis
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Hyperpigmentation Associated with the Use of Topical Cidofovir for Treatment of Trichodysplasia Spinulosa in an Immunosuppressed Adult: Case Report and Review of the Literature
- Hypothesis: platelet-rich plasma as an adjunct therapy for eczema targeting inflammation, skin barrier repair, and chronic recurrence
- Skin Appendage Proteins of Tetrapods: Building Blocks of Claws, Feathers, Hair and Other Cornified Epithelial Structures
- Contents
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Ichthyosis with confetti: clinics, molecular genetics and management
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Recent advances in congenital ichthyoses
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- New developments in the molecular treatment of ichthyosis: review of the literature
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines