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Research 30 of 1000+
- Decreased Androgen Receptor Gene Methylation in Premature Pubarche: A Novel Pathogenetic Mechanism?
- Premature pubarche during minipuberty – literature review and two case reports
- Evaluation of Premature Pubarche Cases: A Single CenterExperience
- Childhood Obesity with Resting State Functional Connectivity and Premature Pubarche with Neuroimaging Methods A Systematic Review
- Prematüre Pubarş Olgularının Değerlendirilmesi: Tek Merkez Deneyimi
- Precocious Pubarche in a 7-Year-Old Patient. A Case Report
- Congenital adrenal hyperplasia
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- The Relationship Between Acne and Other Hyperandrogenism Signs
- Nonclassic Congenital Adrenal Hyperplasia: An Overview
- The pediatric origins of polycystic ovary syndrome
- Nonclassic adrenal hyperplasia
- Precocious Puberty
- Management of polycystic ovary syndrome in adolescence
- An Update of Congenital Adrenal Hyperplasia
- Serum C-19 steroid sulphates in females with clinical hyperandrogenism
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome
- Pelvic ultrasound and color Doppler findings in different isosexual precocities
- The effect of gonadoliberin analog treatment in precocious puberty on polycystic ovarian syndrome prevalence in adulthood
- Insulin Resistance and Polycystic Ovary Syndrome
- Polycystic ovary syndrome
- Congenital Adrenal Hyperplasia
- Protective effects of melatonin against metabolic and reproductive disturbances in polycystic ovary syndrome in rats
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Managing polycystic ovary syndrome in primary care
- CYP21A2 Mutations in Women with Polycystic Ovary Syndrome (PCOS)
- Acne
- Cardiometabolic and neuroimaging correlates of cognitive function in polycystic ovary syndrome
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency