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Research 811–840 of 1000+
- The Rotterdam Study: 2016 objectives and design update
- Mesenchymal–epithelial interactions during hair follicle morphogenesis and cycling
- Androgen Therapy in Women: An Endocrine Society Clinical Practice Guideline
- Mucocutaneous reactions to chemotherapy
- Genetic, hormonal and metabolic aspects of PCOS: an update
- Polycystic Ovary Syndrome
- Interrelation of immunity and tissue repair or regeneration
- Is COVID-19 Gender-sensitive?
- Female pattern hair loss
- Adverse Side Effects of 5α‐Reductase Inhibitors Therapy: Persistent Diminished Libido and Erectile Dysfunction and Depression in a Subset of Patients
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- Telogen Effluvium
- The British Society for Rheumatology guideline for the management of systemic lupus erythematosus in adults
- Dermatoses of pregnancy
- The diagnosis and treatment of iron deficiency and its potential relationship to hair loss
- Stem cell niches in mammals
- Evaluation and treatment of male and female pattern hair loss
- Hair follicle differentiation and regulation.
- Sex differences in the hypothalamic–pituitary–adrenal axis’ response to stress: an important role for gonadal hormones
- Clinical significance of dermoscopy in alopecia areata: analysis of 300 cases
- Ethnicity, obesity and the prevalence of impaired glucose tolerance and type 2 diabetes in PCOS: a systematic review and meta-regression
- COVID-19 and Sex Differences
- Fibrous scaffolds potentiate the paracrine function of mesenchymal stem cells: A new dimension in cell-material interaction
- ATP-dependent chromatin remodeling during mammalian development
- A placebo-controlled, double-blind crossover study of fluoxetine in trichotillomania
- Epigenetic control of adult stem cell function
- Cutaneous Scarring: Basic Science, Current Treatments, and Future Directions
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Erectile Dysfunction in Young Men—A Review of the Prevalence and Risk Factors