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Research 151–180 of 1000+
- Epidemiological Assessment of Testosterone Levels in Women Population: A Factorial Analysis of Cell Proliferation
- The role of protein lactylation in skin diseases: from molecular mechanisms to potential therapeutics
- Low Level Laser and Light Therapy
- Alopecia
- Biology and Genetics of Hair
- MANAGEMENT OF ENDOCRINE DISEASE Hyperandrogenic states in women: pitfalls in laboratory diagnosis
- Hypertrichosis induced by latanoprost
- Elevated fasting insulin is associated with cardiovascular and metabolic risk in women with polycystic ovary syndrome
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- Polycystic Ovary Syndrome: Etiology, Current Management, and Future Therapeutics
- Diagnosis, Pathogenesis and Management of Polycystic Ovary Syndrome
- Erosive Pustular Dermatosis: Delving into Etiopathogenesis and Management
- First Symposium of Ichthyosis Experts
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- Cellular Senescence and Aging in Myotonic Dystrophy
- Pathophysiology and Nutritional Approaches in Polycystic Ovary Syndrome (PCOS): A Comprehensive Review
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Society for Endocrinology Clinical Practice Guideline for the Evaluation of Androgen Excess in Women
- New developments in the molecular treatment of ichthyosis: review of the literature
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- The good, the bad, and the ugly facets of insulin resistance
- Vitisin A Outperforms Cyanidin-3-O-Glucoside in Triglyceride Reduction by Modulating Hepatic Lipogenesis and Fatty Acid β-Oxidation
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Exploring lncRNA-Mediated Mechanisms in Muscle Regulation and Their Implications for Duchenne Muscular Dystrophy
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- The Link Between Obesity and the Skin
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome