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Research 121–150 of 1000+
- [Androgenetic alopecia].
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Cyberspace Chat: Beyond genetics part III: evidence that lifestyle choices may impact hair loss in androgenetic alopecia
- Investigating the Genetic Association of Selected Candidate Loci with Alopecia Areata Susceptibility in Jordanian Patients
- BH26 First reported case of lichen planopilaris in siblings: evidence for a genetic link?
- Development of polycystic ovary syndrome: involvement of genetic and environmental factors
- Molecular epidemiology of hypospadias: Review of genetic and environmental risk factors
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Delving into diversity: exploring different risk factors of premature greying of hair
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- The genetic link between thyroid dysfunction and alopecia areata: a bidirectional two-sample Mendelian randomization study
- Androgenetic Alopecia in Polycystic Ovary Syndrome: A Cutaneous Marker of Systemic Metabo-inflammatory and Endocrine Dysfunction: A Narrative Review
- Role of genetics and sex steroid hormones in male androgenetic alopecia and female pattern hair loss: An update of what we now know
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- The possibilities of correction of premature greying of hair and involutive hair changes
- Anhidrotic Ectodermal Dysplasia: Predisposition to Bronchial Disease
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- Intrinsic factors in the pathogenesis of hidradenitis suppurativa: Genetics, hormones, and the microbiome
- Genetic Susceptibility to Alopecia
- Association between androgenetic alopecia and cardiovascular diseases: a genetic correlation and Mendelian randomization study
- The Successful Treatment of Alopecia Areata with Platelet Rich Plasma in a Case of Twins with Genetic Risk for Autoimmune Disorders
- The genetics of androgenetic alopecia
- Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker
- Racial variations in COVID‐19 deaths may be due to androgen receptor genetic variants associated with prostate cancer and androgenetic alopecia. Are anti‐androgens a potential treatment for COVID‐19?
- In Search of New Therapeutics—Molecular Aspects of the PCOS Pathophysiology: Genetics, Hormones, Metabolism and Beyond
- A Review on Unraveling the Complexity of Autoimmune Skin Disorders: Genetic Influences, Environmental Triggers and Innovative Management Approaches
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- Alopecia Areata
- Familial Frontal Fibrosing Alopecia Occurs Early in Daughters With Affected Mothers: A Case Report and a Review of the Literature