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Research 61–90 of 1000+
- Polycystic Ovary Syndrome: A Comprehensive Review of Its Clinical Presentation, Comorbidities, Long-Term Complications and Management
- A Nonredundant Human Protein Chip for Antibody Screening and Serum Profiling
- Dermatologic applications of direct-to-consumer genomic analysis
- Genetics and Epigenetics of Polycystic Ovary Syndrome
- Rare Germline Pathogenic Variants Identified by Multigene Panel Testing and the Risk of Aggressive Prostate Cancer
- Unscrewing DHT-Blocking Properties of Allium Cepa Extract: Virtual Screening of active Compounds against 5-Alpha Reductase and Evaluation of Adme/T Properties of Compounds
- Relationship between glucose homeostatic disorders and testosterone in adult Nigerian women with polycystic ovary syndrome
- Advice on the safe introduction and continued use of isotretinoin in acne in the U.K. 2010
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Female pattern hair loss—An update
- Dramatic Clinical Improvement With Biotin Mega‐Dose Therapy in a Neonate With Holocarboxylase Synthetase Deficiency
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- The Female Pattern Hair Loss: Review of Etiopathogenesis and Diagnosis
- An unusual presentation of X-linked adrenoleukodystrophy
- Medical Technologies: Pharmaceutical Cosmetology, Cosmeceuticals – Opportunities and Limitations
- Molecular Aspects of Polycystic Ovarian Syndrome in Female Population in Karnataka at the Southwestern Region of India
- Pediatric adrenocortical carcinoma complicated by uric acid nephrolithiasis: a unique case report
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Updates to Male Infertility: AUA/ASRM Guideline (2024)
- The First Visit: Consult and Workup Before Sperm Banking
- Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic?
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- What does the research say about androgen use and cerebrovascular events?
- Nonclassic adrenal hyperplasia
- In vitro hair follicle growth model for drug testing
- ASSESSMENT OF SERUM LEVELS OF ANTIGLIADIN ANTIBODIES (IgG and IgA) IN PATIENTS WITH ALOPECIA AREATA AND THEIR RELATION TO SEVERITY OF THE DISEASE
- Gender-Affirming Hormone Therapy for Transgender Men