Search
for
Sort by
Research 30 of 97
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond
- Highlights
- Nonclassic adrenal hyperplasia
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Intraethnic variation in steroid-5-alpha-reductase polymorphisms in prostate cancer patients: a potential factor implicated in 5-alpha-reductase inhibitor treatment
- Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic?
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Androgenic Alopecia: Cross-Talk Between Cell Signal Transduction Pathways
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- In Silico Promoter Motif Analysis of Human Fertility-Related Genes
- Congenital Adrenal Hyperplasia
- E-Poster
- Investigating the Safety and Efficacy of Platelet-Rich Plasma (PRP) Treatment for Female Androgenetic Alopecia: Review of the Literature
- Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty
- Genetic Defects of Female Sexual Differentiation
- DHEA and TNF-α: Key Factors in Managing Polycystic Ovary Syndrome in Iraqi Females
- Unravelling the link between insulin resistance and androgen excess
- Androgen excess: a hallmark of polycystic ovary syndrome
- Modelling androgen synthesis and action during human sexual differentiation
- Androgenetic Alopecia in Polycystic Ovary Syndrome: A Cutaneous Marker of Systemic Metabo-inflammatory and Endocrine Dysfunction: A Narrative Review
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- Causal Relationship Between Blood Metabolomics and Female Pattern Hair Loss: A Bidirectional Mendelian Randomization Study
- Comorbidities in Androgenetic Alopecia: A Comprehensive Review
- Omega-6 highly unsaturated fatty acids in Leydig cells facilitate male sex hormone production
- Anabolic androgenic steroids and carcinogenicity focusing on Leydig cell: a literature review
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin