Search
forResearch 10 of 384
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- 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
- An Approach to the Patient With Hirsutism
- Approach to androgen excess in women: Clinical and biochemical insights
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Common Forms of Congenital Adrenal Hyperplasia
- A case of 21-hydroxylase deficiency in Turner′s syndrome and literature review
- Society for Endocrinology Clinical Practice Guideline for the Evaluation of Androgen Excess in Women
- Congenital adrenal hyperplasia
- Influence of Genotype and Hyperandrogenism on Sexual Function in Women With Congenital Adrenal Hyperplasia
Learn
— no results
Try a deeper search in learn →Community
— no results
Try a deeper search in community →