Search
for
Sort by
Research 211–240 of 1000+
- Understanding Polycystic Ovary Syndrome
- Dermatologic care of the transgender patient - eScholarship
- Sex hormones and related compounds, including hormonal contraceptives
- Segmental hair analysis as a retrospective testosterone diary: possibilities and pitfalls
- The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology
- Anorexia Nervosa and Bulimia Nervosa
- Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome
- Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome (PCOS)
- Pharmacology of anabolic steroids
- An Update of Congenital Adrenal Hyperplasia
- 9 Role of 5α-reductase in health and disease
- Congenital Adrenal Hyperplasia
- Endocrine-skin interactions
- Current evaluation of amenorrhea
- Congenital adrenal hyperplasia
- Improving selective androgen receptor modulator discovery and preclinical evaluation
- Indirect clinical markers for the detection of anabolic steroid abuse beyond the conventional doping control in athletes
- Familial frontal fibrosing alopecia: A cross‐sectional study of 20 cases from nine families
- Transmasculine Hormone Therapy
- Gonadal Sex Steroids: Production, Action and Interactions in Mammals
- Muscle pain in a woman with congenital adrenal hyperplasia due to 21-hydroxylase deficiency resolved with testosterone therapy. A case report with 10 years of follow-up
- Local synthesis and function of neuro-estrogen and neuro-androgen: impact on the hippocampus-related cognition and neuronal plasticity
- Farmácia Aliança - Maia
- SUMMARIES OF PAPERS
- Menopause - Andropause - Anti-Aging 2008, 11.-13. Dezember 2008, Wien - Abstracts
- Men??s Health
- APECED: JAK Inhibition in an Adult Case with Long-Term Follow-up
- MULTIPLE HEMANGIOMAS OF THE TONGUE AND ORAL CAVITY IN A MYOTONIC DYSTROPHY TYPE 1 PATIENT: A CASE REPORT
- Acrodermatitis Enteropathica: A Case Report Involving a Delayed Diagnosis
- Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome