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Research 91–120 of 628
- Congenital Adrenal Hyperplasia
- Sexual function in women with androgen excess disorders: classic forms of congenital adrenal hyperplasia and polycystic ovary syndrome
- 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
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Dermatologic manifestations of endocrine disorders
- Mister XX
- Structure and Expression of a New Complementary DNA Encoding the almost Exclusive 3β-Hydroxysteroid Dehydrogenase/Δ<sup>5</sup>-Δ<sup>4</sup>-lsomerase in Human Adrenals and Gonads
- What does acne genetics teach us about disease pathogenesis?
- Genetic Defects of Female Sexual Differentiation
- Polycystic ovary syndrome and the differential diagnosis of hyperandrogenism
- Clinical relevance of testosterone and dihydrotestosterone metabolism in women
- An Adult With Hair Loss! a Rare Case of Non-Classical 3β Hydroxysteroid Dehydrogenase (3β HSD) Deficiency
- Hyperandrogenism: Acne and Hirsutism
- Hyperandrogenism: Acne and Hirsutism
- Hyperandrogenism: Acne and Hirsutism
- Hyperandrogenism: Acne and Hirsutism
- Clinical Presentation of Polycystic Ovary Syndrome
- Practical approaches to the use of markers of biochemical hyperandrogenism in women
- Testicular Steroidogenesis
- Acne Syndromes and Mosaicism
- An unusual circulating steroid profile in a virilized postmenopausal woman
- Hirsutism and Hypertrichosis
- Alternative androgen pathways
- Difficult and rare forms of acne
- Approach to androgen excess in women: Clinical and biochemical insights
- Mixed Form of Hirsutism in Adolescent Females and Laser Therapy
- Society for Endocrinology Clinical Practice Guideline for the Evaluation of Androgen Excess in Women
- Serum AMH levels in the differential diagnosis of hyperandrogenemic conditions
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency