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Research 931–960 of 935
- A benign cause of hyperandrogenism in a postmenopausal woman
- Parity-related variation in cortisol concentrations in hair during pregnancy and in the postpartum period: a prospective cohort study
- Melampus and the cure of Proetus’ daughters
- IMPROVEMENT OF ALOPECIA AND DECREASES IN HAIR CORTISOL AND DIHYDROTESTOSTERONE CONCENTRATIONS AFTER THE TOPICAL USE OF PLANT EXTRACTS IN MEN WITH ANDROGENETIC ALOPECIA
- Identification of a new plant extract for androgenic alopecia treatment using a non-radioactive human hair dermal papilla cell-based assay
- SAT338 Desmopressin Stimulation Test As A Valuable Tool In Establishing Cushing Syndrome Etiology
- Results of clinical examinations, laboratory tests, and ultrasonography in dogs with pituitary-dependent hyperadrenocorticism treated with trilostane
- Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status
- Congenital Adrenal Hyperplasia
- Congenital Adrenal Hyperplasia
- Hyperadrenocorticism associated with adrenocortical tumor or nodular hyperplasia of the adrenal gland in ferrets: 50 cases (1987-1991)
- Trilostane treatment of a dog with functional adrenocortical neoplasia
- Differential Diagnosis of Hyperandrogenism in Women with Polycystic Ovary Syndrome
- Congenital adrenal hyperplasia
- The Use of Trilostane for the Treatment of Alopecia X in Alaskan Malamutes
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- Pituitary-dependent hyperadrenocorticism in a shi tzu dog treated with twice-daily oral trilostane: a case report
- Nonclassic adrenal hyperplasia
- Concurrent hyperadrenocorticism in a minature schnauzer with severe <i>Trichophyton mentagrophytes</i> infection
- Heterozygous 21‐hydroxylasedeficiency as a cause of hyperandrogenism
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Pattern alopecia in a miniature pinscher dog
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- Nonclassic Congenital Adrenal Hyperplasia
- Non-classic congenital adrenal hyperplasia
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Congenital adrenal hyperplasia
- May AMH levels distinguish LOCAH from PCOS among hirsute women?
- Atypical Cushing's Syndrome in Dogs: Arguments For and Against
- The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis