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Research 61–90 of 1000+
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Polycystic ovary syndrome in men
- Frontal fibrosing alopecia
- Cutaneous manifestation of polycystic ovary syndrome
- Fox-Fordyce Disease
- Polyzystisches Ovar-Syndrom (PCOS)
- Polycystic Ovary Syndrome: Management of a Long-Term Condition in Primary Care
- Virilization beyond menopause: an uncommon ovarian tumor in an elderly patient with multimodality imaging and pathologic correlation
- Polycystic Ovary Syndrome: A Complex Interplay of Hormones and Metabolism
- Understanding Polycystic Ovary Syndrome: A Comprehensive Guide
- Supplementary Material for: The Role of Fibrosis in Androgenetic Alopecia: Mechanisms and Implications
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- PMON281 PERSISTENT VIRILIZATION AND VASOMOTOR SYMPTOMS IN A TRANSMAN 5-YEARS POST TESTOSTERONE WITHDRAWAL
- Lipedematous scalp with lipedematous alopecia: A case report
- An Unusual but Important Cause of Hyperandrogenism in Women
- A comparison of self-reported signs of facial aging among women in Australia vs. those in the United States, United Kingdom, and Canada
- Cosmetic Surgery Considerations in the Female Patient
- Non‐endocrine alopecia
- Androgens and Hirsutism in a Large Cohort of Portuguese Women
- 5 Dihydrotestosterone metabolism
- Male polycystic ovarian syndrome phenotype: a meta-analysis of endocrine-metabolic dysregulation in fathers and brothers of PCOS-affected women
- Hair loss in women
- Dermatologic Manifestations of Polycystic Ovary Syndrome
- An update on the pathophysiology of female pattern hair loss
- [Long-term treatment of virilized women with cyproterone acetate (author's transl)].
- Frontal Fibrosing Alopecia in Men: A Review of the Literature
- Postmenopausal Frontal Fibrosing Alopecia
- Postmenopausal frontal fibrosing alopecia. Scarring alopecia in a pattern distribution
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations