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Research 931–960 of 1000+
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- The Role of Medical Language in Changing Public Perceptions of Illness
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Finasteride and Its Potential for the Treatment of Female Pattern Hair Loss: Evidence to Date
- Manifestation of Hyperandrogenism in the Continuous Light Exposure-Induced PCOS Rat Model
- Polycystic ovary syndrome: A review for dermatologists
- Hormonal therapies for acne
- Relationship between betacoronaviruses and the endocrine system: a new key to understand the COVID-19 pandemic—A comprehensive review
- An Intrinsic Oscillation of Gene Networks Inside Hair Follicle Stem Cells: An Additional Layer That Can Modulate Hair Stem Cell Activities
- Dermatologie care behind bars
- Neuropsychological Assessment in Elderly Men with Benign Prostatic Hyperplasia Treated with Dutasteride
- Androgenetic alopecia: combing the hair follicle signaling pathways for new therapeutic targets and more effective treatment options
- Physiopathological role of the enzymatic complex 5α-reductase and 3α/β-hydroxysteroid oxidoreductase in the generation of progesterone and testosterone neuroactive metabolites
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Risk Factors for Male Lower Urinary Tract Symptoms: The Role of Metabolic Syndrome and Androgenetic Alopecia in a Latin American Population
- Gender Surgery Beyond Chest and Genitals: Current Insurance Landscape
- AROMA THERAPY: AN ART OF HEALING
- Steroid 5α-reductase 2 deficiency leads to reduced dominance-related and impulse-control behaviors
- Is the metabolism of testosterone to 5α-dihydrotestosterone required for androgen action in the skin?
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Predicting Human Appearance from DNA for Forensic Investigations
- Infertility: Evaluation and Initial Management
- Advances in Hair Diseases
- 5-alpha Reductase inhibitors and risk of male breast cancer: a systematic review and meta-analysis
- “Spigo nardo”: from the Erbario Estense a possible solution for its taxonomical attribution
- Early-onset baldness and the risk of aggressive prostate cancer: findings from a case–control study
- Optimal Management of Frontal Fibrosing Alopecia: A Practical Guide