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- Heterozygous 21‐hydroxylasedeficiency as a cause of hyperandrogenism
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency
- Acne-Associated Syndromes
- Differential Diagnosis of Hyperandrogenism in Women with Polycystic Ovary Syndrome
- Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency
- Female Hirsutism: Pathophysiological Considerations and Therapeutic Implications*
- The eye and the skin in endocrine metabolic diseases
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- The Role of Probiotics and Synbiotics on Hirsutism
- Testicular Steroidogenesis
- An Update of Congenital Adrenal Hyperplasia
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- Abstracts from the Symposium on the Pathophysiology of Hair Growth Organized by the Institute of Dermatology at the Royal Society of Medicine, 29 October 1987
- 46,XY DSD due to impaired androgen production
- Penis Endocrinology
- Use of cyproterone acetate (CPA) in the treatment of acne, hirsutism and virilism
- Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency revisited: an update with a special focus on adolescent and adult women
- Non-classic congenital adrenal hyperplasia
- The Effect of Simvastatin on Plasma Steroid Hormone Levels in Metformin-Treated Women with Non-Classic Congenital Adrenal Hyperplasia
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- Cardiometabolic risk factors in women with non-classic congenital adrenal hyperplasia
- Unusual presentation with polymenorrhagia and markedly high 17-hydroxy progesterone levels in a lady with Non-Classic Congenital Adrenal Hyperplasia.
- 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
- Severe Hirsutism in Non Classic Congenital Adrenal Hyperplasia: A Case Report and Literature Review
- MON-369 Treatment of Nonclassic 11-Hydroxylase Deficiency with "Hair, Skin, and Nails," an Over-the-Counter, Insulin Sensitizing Vitamin/Mineral Supplement
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update