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Research 901–930 of 1000+
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Efficacy and tolerability of oral bicalutamide in forty postmenopausal women with female pattern hair loss: a retrospective study
- PRIDE Complex (Papulopustules and/or Paronychia, Regulatory Abnormalities of Hair Growth, Itching, Dryness Due to EGFR Inhibitors)
- Convergent evolution has led to the loss of claw proteins in snakes and worm lizards
- A linear and reticulate crusted keratotic papulopustular eruption: a rare presentation of PRIDE (Papulopustules and/or paronychia, Regulatory abnormalities of hair growth, Itching, and Dryness due to Epidermal growth factor receptor inhibitors) complex
- BH10 Unequal National Health Service wig provision: toupée or no toupée, that is the question?
- Patient-reported treatment outcomes and safety of direct-to-consumer teledermatology for finasteride treatment in male androgenetic alopecia: A cross-sectional study
- Genital Dermatology
- Evaluation of serum level of biotin and effect of biotin replacement therapy in patients with telegon effluvium
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Structural and Immunocytochemical Characterization of Keratinization in Vertebrate Epidermis and Epidermal Derivatives
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Vitamin D and skin diseases: A review
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- COVID‐19 and dermatology: a comprehensive guide for dermatologists
- The influence of interferon on healthy and diseased skin
- “‘You lose your hair, what’s the big deal?’ I was so embarrassed, I was so self-conscious, I was so depressed:” a qualitative interview study to understand the psychosocial burden of alopecia areata
- Analysis of Mercury in Sequential Micrometer Segments of Single Hair Strands of Fish-Eaters
- Formulation-by-Design of Efinaconazole Spanlastic Nanovesicles for Transungual Delivery Using Statistical Risk Management and Multivariate Analytical Techniques
- Poster Presentations
- In Vitro Methodologies to Evaluate the Effects of Hair Care Products on Hair Fiber
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- ChatGPT in medicine: Evaluating psoriasis patient concerns
- In vitro biodegradation of hair from different animal species by Microsporum canis
- Building Models for Keratin Disorders