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Research 391–420 of 1000+
- Oral Manifestations of Hematologic and Nutritional Diseases
- Alopecia areata update
- Significance of the S100A4 Protein in Psoriasis
- Are sex discordant outcomes in COVID-19 related to sex hormones?
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- Toxic shock syndrome: Recent developments in pathogenesis
- Marie Antoinette Syndrome
- Hair Restoration Surgery: The State of the Art
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- Sp6 downregulation of follistatin gene expression in ameloblasts
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Roles of steroid sulfatase in brain and other tissues
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- INTERFERONS IN DERMATOLOGY
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Is there any relationship between decreased AgNOR protein synthesis and human hair loss?
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Congenital adrenal hyperplasia
- Hormonal regulation in male androgenetic alopecia—Sex hormones and beyond: Evidence from recent genetic studies
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Androgen Receptor in Human Health: A Potential Therapeutic Target
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- Androgen Receptor Polymorphism-Dependent Variation in Prostate-Specific Antigen Concentrations of European Men
- Male androgenetic alopecia (Part II)