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Research 30 of 1000+
- Study on Changes of 19 Steroids in Plasma From 9 Diagnosed Patients With P450 Oxidoreductase Deficiency
- Defects in Androgen Biosynthesis Causing 46,XY Disorders of Sexual Development
- Steroidogenesis of the testis – new genes and pathways
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Clinical analysis of 78 patients with non-classical 21-hydroxylase deficiency
- Physiopathological role of the enzymatic complex 5α-reductase and 3α/β-hydroxysteroid oxidoreductase in the generation of progesterone and testosterone neuroactive metabolites
- 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
- Nonclassic congenital adrenal hyperplasia
- Nonclassic Congenital Adrenal Hyperplasia
- Nonclassic adrenal hyperplasia
- Congenital adrenal hyperplasia
- Helpful diagnostic markers of steroidogenesis for defining hyperandrogenemia in hirsute women
- Integrating multi-omics analyses of Nonomuraea dietziae to reveal the role of soybean oil in [(4′-OH)MeLeu]4-CsA overproduction
- Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- Clinical biochemistry of dihydrotestosterone
- Xenobiotica-metabolizing enzymes in the skin of rat, mouse, pig, guinea pig, man, and in human skin models
- Immunological and Metabolic Causes of Infertility in Polycystic Ovary Syndrome
- Glucocorticoids and mineralocorticoids in hair: facilitating accurate diagnosis of adrenal-related endocrine disorders
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- 46,XY DSD due to impaired androgen production
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- Genetic Defects of Female Sexual Differentiation
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- Cutaneous Androgen Metabolism: Basic Research and Clinical Perspectives
- Novel inhibitors of 5α-reductase
- Vitamin D, Lipid Metabolism and Prostate Cancer
- Androgenetic Alopecia
- Regulation of masculinization: androgen signalling for external genitalia development