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Research 61–90 of 538
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Approach to the Patient: Hirsutism
- Case 1: Clitoromegaly, Oligomenorrhea, and Hirsutism in a 17-year-old Transgender Male
- A Detailed Investigation of Hirsutism in a Turkish Population: Idiopathic Hyperandrogenemia as a Perplexing Issue
- The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report
- Polycystic Ovary Syndrome and NC-CAH: Distinct Characteristics and Common Findings. A Systematic Review
- Hyperandrogenism in Adolescent Girls
- Mixed Form of Hirsutism in Adolescent Females and Laser Therapy
- Acne in Dark Skin
- Endo&Art why Diana is depicted with mild androgenic alopecia?
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Clinical, Laboratory, and Radiological Diagnosis of Hyperandrogenism
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- Congenital Adrenal Hyperplasia
- Voice changes in reproductive disorders, thyroid disorders and diabetes: a review
- Defects in Androgen Biosynthesis Causing 46,XY Disorders of Sexual Development
- Secondary Amenorrhea and Clinical Hyperandrogenism in a 34-Year-Old Female: Polycystic Ovary Syndrome or Not?
- Congenital Adrenal Hyperplasia
- 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
- Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- Measuring steroids in hair opens up possibilities to identify congenital adrenal hyperplasia in developing countries
- Diagnostic imaging in congenital adrenal hyperplasia – how does it help?
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Severe impact of late diagnosis of congenital adrenal hyperplasia on gender identity, sexual orientation and function: case report and review of the literature
- Congenital Adrenal Hyperplasia
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status