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Research 30 of 627
- Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status
- Spironolactone therapy in hypertrichosis
- The laboratory in the multidisciplinary diagnosis of differences or disorders of sex development (DSD)
- The effect of hormones of the hypothalamic-pituitary-target gland axes in a kidney-yang deficiency syndrome model
- Central Diabetes Insipidus and Hypothalamic Type of Hypopituitarism Associated with Atypical Location of Rathke's Cleft Cyst
- Clinical and Imagistic Aspects in Dog’s Hyperadrenocorticism Determined by Pituitary and Adrenal Nodules with Secretory Function
- Unusual presentation with polymenorrhagia and markedly high 17-hydroxy progesterone levels in a lady with Non-Classic Congenital Adrenal Hyperplasia.
- Pituitary-dependent hyperadrenocorticism in a cat
- Hyperandrogenic eumenorrheic NON-PCOS women versus women with PCOS after the GnRH-agonist stimulation test preceded by suppression of adrenal steroidogenesis with dexamethasone
- Idiopathic isolated adrenocorticotropic hormone deficiency combined with testicular germ cell tumor: Case report
- Congenital adrenal hyperplasia
- Challenges in diagnosis and treatment of Cushing disease in a 12-year-old boy
- Hyperandrogenemia in an ethnically heterogeneous cohort of Midwestern United States diabetic gestations
- The Use of Trilostane for the Treatment of Alopecia X in Alaskan Malamutes
- Hyperadrenocorticism associated with adrenocortical tumor or nodular hyperplasia of the adrenal gland in ferrets: 50 cases (1987-1991)
- Role of the ACTH/MC2R System in the Hair Cycle in Mice
- Pituitary Effects of Metformin in Men With Early‐Onset Androgenic Alopecia
- The human skin as a hormone target and an endocrine gland
- The Hormonal Background of Hair Loss in Non-Scarring Alopecias
- Rapid Intravenous Administration of Corticotropin as a Test of Adrenocortical Insufficiency
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- Physiology of the Hypothalamic Pituitary Gonadal Axis in the Male
- Diagnosis, Manifestations, Laboratory Investigations, and Prognosis in Pediatric and Adult Cushing’s Disease in a Large Center in China
- Gene expression profile of human follicle dermal papilla cells in response to <i>Camellia japonica</i> phytoplacenta extract
- Pelvic ultrasound and color Doppler findings in different isosexual precocities
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Testosterone Therapy in Premenopausal Women
- Clinical relevance of testosterone and dihydrotestosterone metabolism in women
- 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
- Physiopathological role of the enzymatic complex 5α-reductase and 3α/β-hydroxysteroid oxidoreductase in the generation of progesterone and testosterone neuroactive metabolites