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Research 511–540 of 516
- Mediterranean Basin Erica Species: Traditional Uses, Phytochemistry and Pharmacological Properties
- Illness and femininity in Hilary Mantel’s Giving Up the Ghost (2003)
- Use of 5% Topical Minoxidil Application for Telogen Effluvium: An Open‐Label Single‐Arm Clinical Trial
- The Progress in Bioprinting and Its Potential Impact on Health-Related Quality of Life
- Lifestyle drugs: concept and impact on society
- Back to the beginning: a retrospective review of the early <i>Forums</i>
- 46, XY Disorder of Sexual Development with Ambiguous Female External Genitalia: A Case Report
- 5α Reductase Deficiency—a Rare Cause of Ambiguous Genitalia and Gender Dysphoria
- Male pseudohermaphroditism due to 17β-hydroxysteroid dehydrogenase deficiency: Studies on the natural history of the defect and effect of androgens on gender role
- 46,XY DSD due to impaired androgen production
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- Steroid 17β-hydroxysteroid dehydrogenase deficiency in man: An inherited form of male pseudohermaphroditism
- Congenital adrenal hyperplasia
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Disorders of Sex Development
- Severe impact of late diagnosis of congenital adrenal hyperplasia on gender identity, sexual orientation and function: case report and review of the literature
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- 5-Alpha-reductase deficiency in a Saudi "girl"
- (673) Seminoma in SRY-Negative 46, XX Testicular Disorder of Sex Development Presenting as Acute Abdomen: An Extremely Rare Case Report
- ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- The articulations of Adam's rib with the lower urinary tract
- MALE PSEUDOHERMAPHRODITISM DUE TO 17β-HYDROXYSTEROID DEHYDROGENASE DEFICIENCY: STUDIES ON THE NATURAL HISTORY OF THE DEFECT AND EFFECT OF ANDROGENS ON GENDER ROLE
- Mister XX
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Novel Missense Mutation in the P-Box of Androgen Receptor in a Patient with Androgen Insensitivity Syndrome
- Disorders in Male Sexual Differentiation Due to 5α-Reductase-2 Deficiency
- The 5 Alpha-Reductase Isozyme Family: A Review of Basic Biology and Their Role in Human Diseases
- 9 Role of 5α-reductase in health and disease
- Congenital Adrenal Hyperplasia