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Research 31–60 of 552
- Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management
- Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency revisited: an update with a special focus on adolescent and adult women
- Congenital Adrenal Hyperplasia
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Congenital Adrenal Hyperplasia
- Gene-wide association study between the aromatase gene (<i>CYP19A1</i>) and female pattern hair loss
- Nonclassic adrenal hyperplasia
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Non-classic congenital adrenal hyperplasia
- Studying the genetic predisposing factors in the pathogenesis of acne vulgaris
- Aromatase deficiency in a male patient - Case report and review of the literature.
- Hepatotoxicity with low- and ultralow-dose flutamide: a surveillance study on 203 hyperandrogenic young females
- Inhibition of 17α-hydroxylase/C17,20 lyase reduces gating deficits consequent to dopaminergic activation
- Does maternal exposure to artificial food coloring additives increase oxidative stress in the skin of rats?
- 11α-Hydroxyprogesterone, a potent 11β-hydroxysteroid dehydrogenase inhibitor, is metabolised by steroid-5α-reductase and cytochrome P450 17α-hydroxylase/17,20-lyase to produce C11α-derivatives of 21-deoxycortisol and 11-hydroxyandrostenedione in vitro
- Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker
- Early onset female pattern hair loss: a case–control study for analyzing clinical features and genetic variants
- Estrogen regulates the expression of retinoic acid synthesis enzymes and binding proteins in mouse skin
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Effect of <i>Eurycoma longifolia</i> Extract on Testosterone Synthesis in TM3 Leydig Cells under Oxidative Stress
- A case of 21-hydroxylase deficiency in Turner′s syndrome and literature review
- Nonclassical Congenital Adrenal Hyperplasia and Pregnancy
- Single-cell analysis of 2,3,7,8-tetrachlorodibenzo- <i>p</i> -dioxin (TCDD)-treated murine skin demonstrates that sebaceous gland differentiation precedes <i>Ahr</i> -dependent seboatrophy with elevated expression of infundibular <i>Blimp1</i>
- Dendrobium officinale polysaccharide improves hair regrowth in androgenetic alopecia mice and is associated with coordinated changes in local steroid metabolism, ESR1 activation, and keratin-related follicular responses
- Study on the mechanism that SNPs related to sex hormone metabolism regulate the imbalance of sex hormones and lead to BPH in rats
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Clinical-Exome Sequencing Unveils the Genetic Landscape of Polycystic Ovarian Syndrome (PCOS) Focusing on Lean and Obese Phenotypes: Implications for Cost-Effective Diagnosis and Personalized Treatment
- Identification of Potential Cytochrome p450c 17 Alpha Inhibitors for the Treatment of PCOS via Scaffold Hopping and Fragment-Based De-Novo Drug Design
- Approaching fertility in congenital adrenal hyperplasia: exploring P30L mutation-induced 21-hydroxylase deficiency with a presentation between non-classical and simple virilizing phenotypes. A case report
- Clinical features of non‐classical 21‐hydroxylase deficiency after normal newborn mass screening