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Research 331–360 of 1000+
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- COVID-19 and Sex Differences
- Workup and Management of Polycystic Ovary Syndrome
- Adult polycystic ovary syndrome begins in childhood
- Cutaneous lupus erythematosus
- Epidemiology and burden of alopecia areata: a systematic review
- Lupus erythematosus: systemic and cutaneous manifestations
- Diuretics
- Cutaneous Lupus Erythematosus
- Androgen sensitivity gateway to COVID‐19 disease severity
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Ehlers-Danlos syndrome: From bedside to bench
- The potential impact of melanosomal pH and metabolism on melanoma
- Diagnostic imaging in congenital adrenal hyperplasia – how does it help?
- Pathophysiological mechanisms implicated in postpartum depression
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Chemotherapy-Induced Alopecia by Docetaxel: Prevalence, Treatment and Prevention
- Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism
- Arzneimitteltherapie der Alopezien
- Loss of the Y Chromosome: A Review of Molecular Mechanisms, Age Inference, and Implications for Men’s Health
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Outbreak of recombinant lumpy skin disease virus in yaks: high mortality and systemic pathogenesis in Qinghai-Tibet Plateau yak herds
- Evaluating the Causal Relationship Between Human Blood Metabolites and the Susceptibility to Alopecia Areata
- Androgen-associated and androgen-independent causes of alopecia and acne in women. Literature review
- Alopecia areata: a review of diagnosis, pathogenesis and the therapeutic landscape
- Endocrinology of the Aging Prostate: Current Concepts
- Evaluation of the predictive capacity of DNA variants associated with straight hair in Europeans
- P448: Identification of a novel RPS6KA3 variant in a female child with features of Coffin-Lowry syndrome: A case study
- Comprehensive Program Planning for the Integration of 21st Century Learning Center After-School Programs with Regular Day Programs and Community Partners.
- Genetic Defects of Female Sexual Differentiation