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Research 691–720 of 1000+
- Successful Management of Folliculitis Decalvans
- Characterization of Hair Follicles in Hirosaki Hairless Rats with Deletion of Basic Hair Keratin Genes. Enlarged Medulla, Loss of Cuticle and Long Catagen
- Skin phenotype diversity across populations: from skin morphology to molecular phenotype
- Descriptive Study of Hairline Patterns amongst Etche People of Rivers State, Nigeria
- Effectiveness and Adverse Drug Reaction Mechanisms Associated with Valproic Acid Use: A Cross-Sectional Prospective Study in Indonesia
- Frontal Fibrosing Alopecia in Men: A Review of the Literature
- Frontal Fibrosing Alopecia in Men: A Review of the Literature
- A Precis of the alopecia (Hair loss) associated with therapies based on nanotechnology and its impact on quality of Life (QoL)
- Hyperinsulinism, Insulin Resistance and Fertility
- Androgenetic alopecia in women
- Selenium for preventing cancer
- Overweight and Obesity in Children and Adolescents
- Epidermal Notch signalling: differentiation, cancer and adhesion
- COVID-19: Pulmonary and Extra Pulmonary Manifestations
- Impact of estrogens in males and androgens in females
- Epithelial Skin Biology
- Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis
- When whorls collide: the development of hair patterns in frizzled 6 mutant mice
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Common variants in the sex hormone-binding globulin gene (SHBG) and polycystic ovary syndrome (PCOS) in Mediterranean women
- Alopecia Universalis Successfully Treated With Adalimumab
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
- Hepatotoxicity with low- and ultralow-dose flutamide: a surveillance study on 203 hyperandrogenic young females
- Anatomy of ageing face
- Expanding the Phenotypic Spectrum of Olmsted Syndrome
- Hair follicle characteristics and fibre production in South American camelids
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Polycystic Ovary Syndrome: Special Diagnostic and Therapeutic Considerations for Children
- Characterization of polycystic ovary syndrome among Flo app users around the world