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Research 31–60 of 1000+
- Mister XX
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- Congenital Adrenal Hyperplasia
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Unusual presentation with polymenorrhagia and markedly high 17-hydroxy progesterone levels in a lady with Non-Classic Congenital Adrenal Hyperplasia.
- Congenital Adrenal Hyperplasia
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Hormonal acne: leading to a paradigm shift in the management of acne
- Androgens and Hirsutism in a Large Cohort of Portuguese Women
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Voice changes in reproductive disorders, thyroid disorders and diabetes: a review
- Hyperandrogenism in polycystic ovary syndrome and adrenal hyperplasia: finding differences to make a specific diagnosis
- Non polycystic ovary syndrome–related endocrine disorders associated with hirsutism
- Severe Hirsutism in Non Classic Congenital Adrenal Hyperplasia: A Case Report and Literature Review
- Treatment of Nonclassic 11-Hydroxylase Deficiency with Ashwagandha Root
- The Evaluation and Management of Hirsutism
- Non-classical congenital adrenal hyperplasia: current insights into clinical implications, diagnosis and treatment
- Ashwagandha root in the treatment of non-classical adrenal hyperplasia
- Relative Prevalence of Different Androgen Excess Disorders in 950 Women Referred because of Clinical Hyperandrogenism
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- The Hirsute Woman: Challenges in Evaluation and Management
- Polycystic Ovary Syndrome and Its Differential Diagnosis
- Hyperandrogenism in Adolescent Girls
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Polycystic Ovary Syndrome and NC-CAH: Distinct Characteristics and Common Findings. A Systematic Review