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Research 61–90 of 1000+
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Overview of Urethral Reconstruction by Tissue Engineering: Current Strategies, Clinical Status and Future Direction
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Pharmacovigilance profiles of three generations of mineralocorticoid receptor antagonists and network toxicology analysis
- Clinical biochemistry of dihydrotestosterone
- Safety of Common Medications for Treating Dermatology Disorders in Pregnant Women
- The First Visit: Consult and Workup Before Sperm Banking
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Specific morphogenetic events in mouse external genitalia sex differentiation are responsive/dependent upon androgens and/or estrogens
- Hormonal Therapies for Individuals with Intersex Conditions
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Androgen Treatment in Adolescent Males With Hypogonadism
- Role of 5 alpha-reductase inhibitors in the management of prostate cancer
- Case Report: Penile Strangulation Secondary to Hair Tourniquet
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- A long-term follow-up study of men born with very low birth weight and their reproductive hormone profile
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- Testosterone: The Male Sex Hormone
- E-Poster
- Estrogen and androgen signaling in the pathogenesis of BPH
- Hox genes in development and beyond
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management
- An Update of Congenital Adrenal Hyperplasia
- Methimazole, Carbimazole, and Congenital Skin Defects
- Congenital Adrenal Hyperplasia
- Congenital Adrenal Hyperplasia