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Research 811–840 of 1000+
- Normal Pubertal Development in Daughters of Women With PCOS: A Controlled Study
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Non-invasive skin measurement methods and diagnostics for vitiligo: a systematic review
- Effects of Egg Shell Membrane Hydrolysates on UVB-radiation-induced Wrinkle Formation in SKH-1 Hairless Mice
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Epigenetic regulation of 5α reductase-1 underlies adaptive plasticity of reproductive function and pubertal timing
- The Role of Probiotics and Synbiotics on Hirsutism
- The association of medications and supplements with human male reproductive health: a systematic review
- Treatment options for alopecia areata
- Pediatric androgenetic alopecia: a retrospective review of clinical characteristics, hormonal assays and metabolic syndrome risk factors in 23 patients
- Abstracts
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Cardiovascular risk markers in premature canities
- A Current Diagnostic and Therapeutic Challenge: Tinea Capitis
- Inheritance-Specific Dysregulation of Th1- and Th17-Associated Cytokines in Alopecia Areata
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Evolution and Trends of Facial Plastic Surgery and Facial Aesthetic Procedures in India: From Awakening to Revival
- Hirsutism-A Comprehensive Update of Embryology, Aetiopathogenesis and Therapeutic Approach
- Medical Therapy for Female Pattern Hair Loss (FPHL)
- Synopsis: 2005 Annual Meeting of the American Society of Andrology
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Proteins in Scalp Hair of Preschool Children
- Characteristics of Androgenetic Alopecia in Asian
- Alopecia and Associated Toxic Agents: A Systematic Review
- Comprehensive treatment of Cronkhite-Canada syndrome: A case report and literature review