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Research 30 of 377
- 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
- INCIDENCE OF VIRILISATION IN SEX CORD STROMAL TUMOURS OF OVARY, A 5- YEAR EXPERIENCE IN A TERTIARY CARE GYNAECOLOGICAL CENTRE
- Congenital Adrenal Hyperplasia
- Clinical Case Seminar: Postmenopausal androgen excess-challenges in diagnostic work-up and management of ovarian thecosis
- Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency
- Epicardial fat thickness in children with classic congenital adrenal hyperplasia
- An Update of Congenital Adrenal Hyperplasia
- Genetic Defects of Female Sexual Differentiation
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Cardiovascular risk factors and events in women with androgen excess
- Congenital adrenal hyperplasia
- A case of androgen-secreting adrenal carcinoma with non-classical congenital adrenal hyperplasia
- Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia
- Pathogenesis and causes of hirsutism
- 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
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- Androgenic disorders
- Severe impact of late diagnosis of congenital adrenal hyperplasia on gender identity, sexual orientation and function: case report and review of the literature
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Congenital Adrenal Hyperplasia
- Alternative androgen pathways
- Mister XX