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Research 30 of 1000+
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- Congenital adrenal hyperplasia
- 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
- Common Forms of Congenital Adrenal Hyperplasia
- Virilism and Ectopic Expression of HSD17B5 in Mature Cystic Teratoma
- An Update of Congenital Adrenal Hyperplasia
- Congenital adrenal hyperplasia
- Vitamin D, Lipid Metabolism and Prostate Cancer
- Unraveling the mechanism of action of cepharanthine for the treatment of novel coronavirus pneumonia (COVID-19) from the perspectives of systematic pharmacology
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency
- Muscle pain in a woman with congenital adrenal hyperplasia due to 21-hydroxylase deficiency resolved with testosterone therapy. A case report with 10 years of follow-up
- Screening for 21-hydroxylase–deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study
- Clinical analysis of 78 patients with non-classical 21-hydroxylase deficiency
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Steroidal 5α-reductase and 17α-hydroxylase/17,20-lyase (CYP17) inhibitors useful in the treatment of prostatic diseases
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- Structure-guided manipulation of the regioselectivity of the cyclosporine A hydroxylase CYP-sb21 from Sebekia benihana
- [Studies on enzyme activities in the hair root in male pattern baldness: glycolytic enzyme, acid hydrolase, transglutaminase and ornithine decarboxylase activities of plucked hair roots].
- Nonclassic adrenal hyperplasia
- A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs
- Nonclassic Congenital Adrenal Hyperplasia
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- Endocrine-skin interactions
- Mister XX
- Serum C-19 steroid sulphates in females with clinical hyperandrogenism
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Congenital Adrenal Hyperplasia
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- Functional characterization and unraveling the structural determinants of novel steroid hydroxylase CYP154C7 from Streptomyces sp. PAMC26508