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Research 91–120 of 402
- Anabolic–Androgenic Steroids and Brain Damage: A Review of Evidence and Medico-Legal Implications
- Newly Developed Targeted Therapies Against the Androgen Receptor in Triple-Negative Breast Cancer: A Review
- Disappearance of a virilizing adrenal tumor following therapy with cyproterone acetate
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- Approaching fertility in congenital adrenal hyperplasia: exploring P30L mutation-induced 21-hydroxylase deficiency with a presentation between non-classical and simple virilizing phenotypes. A case report
- Virilising ovarian tumour in a woman with an adrenal nodule
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- VIRILISING OVARIAN TUMOUR
- Common Forms of Congenital Adrenal Hyperplasia
- [Hirsutism].
- Methods of hair loss evaluation in patients with endocrine disorders.
- Case 1: Clitoromegaly, Oligomenorrhea, and Hirsutism in a 17-year-old Transgender Male
- An Approach to the Patient With Hirsutism
- Adrenocortical tumor in 20 months old female
- [G-proteins, receptor signal transduction, and growth hormone secretion].
- [Long-term treatment of virilized women with cyproterone acetate (author's transl)].
- A case of 21-hydroxylase deficiency in Turner′s syndrome and literature review
- ODP423 Postmenopausal Virilization Secondary to A Rare Left Ovarian Androgen-Secreting Leydig Cell Tumor Localized Using Ovarian Vein Sampling
- Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency
- Congenital Adrenal Hyperplasia
- Nonclassic adrenal hyperplasia
- Nonclassic Congenital Adrenal Hyperplasia
- Nonclassic congenital adrenal hyperplasia
- Congenital adrenal hyperplasia
- Epicardial fat thickness in children with classic congenital adrenal hyperplasia
- Congenital adrenal hyperplasia
- Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia
- 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
- Virilizing insulinoma
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy