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Research 30 of 1000+
- 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
- Adrenocorticotropic Hormone (ACTH) But Not Alpha-Melanocyte Stimulating Hormone (a-MSH) as a Mediator of Adrenalectomy Induced Hair Growth in Mink
- Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status
- SAT338 Desmopressin Stimulation Test As A Valuable Tool In Establishing Cushing Syndrome Etiology
- Role of the ACTH/MC2R System in the Hair Cycle in Mice
- Detection of Functionally Active Melanocortin Receptors and Evidence for an Immunoregulatory Activity of α-Melanocyte-Stimulating Hormone in Human Dermal Papilla Cells
- Results of clinical examinations, laboratory tests, and ultrasonography in dogs with pituitary-dependent hyperadrenocorticism treated with trilostane
- Congenital Adrenal Hyperplasia
- Congenital Adrenal Hyperplasia
- Hyperadrenocorticism associated with adrenocortical tumor or nodular hyperplasia of the adrenal gland in ferrets: 50 cases (1987-1991)
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- Nonclassic adrenal hyperplasia
- Nonclassic Congenital Adrenal Hyperplasia
- Non-classic congenital adrenal hyperplasia
- Trilostane treatment of a dog with functional adrenocortical neoplasia
- Differential Diagnosis of Hyperandrogenism in Women with Polycystic Ovary Syndrome
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Congenital adrenal hyperplasia
- Atypical Cushing's Syndrome in Dogs: Arguments For and Against
- Ketoconazole use in the treatment of ovarian hyperandrogenism
- Congenital adrenal hyperplasia
- The Use of Trilostane for the Treatment of Alopecia X in Alaskan Malamutes
- CYP21A2 Mutations in Women with Polycystic Ovary Syndrome (PCOS)
- May AMH levels distinguish LOCAH from PCOS among hirsute women?
- Concurrent hyperadrenocorticism in a minature schnauzer with severe <i>Trichophyton mentagrophytes</i> infection
- Clinicopathologic and Morphologic Analysis of the Adrenal Gland in Pomeranians with Non-Illness Alopecia
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- Heterozygous 21‐hydroxylasedeficiency as a cause of hyperandrogenism
- Nonclassic Congenital Adrenal Hyperplasia: An Overview
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency