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Research 271–300 of 1000+
- A Comprehensive Approach in Diagnosing the Polycystic Ovary Syndrome
- Ottawa, Ontario, Canada, February 13–16, 2013
- Abstracts
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Polycystic Ovary Syndrome-Associated Acne: The Interplay of Hyperandrogenism, Insulin Resistance, and Therapeutic Strategies
- Polycystic Ovary Syndrome: A Complex Interplay of Hormones and Metabolism
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Genetic Defects of Female Sexual Differentiation
- 211 TRIGLYCERIDEMIA IN CONDITION OF FOOD STRESS IN WOMEN WITH POLYCYSTIC OVARY SYNDROME AND ANDROGENIC ALOPECIA
- Syndromes of Severe Insulin Resistance (SSIRs)
- Cutaneous Reactions to Drugs
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome (PCOS)
- Cutaneous signs in COVID ‐19 patients: A review
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- Polycystic Ovary Syndrome
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Mood disorders and quality of life in polycystic ovary syndrome
- Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat
- Age-related differences in the reproductive and metabolic implications of polycystic ovarian syndrome: findings in an obese, United States population
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia
- Non‐infective mucocutaneous presentations of human immunodeficiency virus infection
- The Multisystem Impact of Long COVID: A Comprehensive Review
- Clinical Findings, Response to Steroid Treatment, and Recurrence Rate in Alopecia Areata Patients with or without a Nonsynonymous Variant of Coiled-Coil Alpha-Helical Rod Protein 1
- Polycystic Ovary Syndrome
- Escobar syndrome (multiple pterygium syndrome) associated with osteogenesis imperfecta: a case report
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Scanning Electron Microscopy Approach for Evaluation of Hair Dyed with Lawsonia inermis Powder: in vitro Study
- BH14 Multiple sclerosis and alopecia areata: drug-induced alopecia areata or coexisting autoimmune phenomena?