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Research 30 of 1000+
- 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)
- Nonclassic Congenital Adrenal Hyperplasia
- 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
- May AMH levels distinguish LOCAH from PCOS among hirsute women?
- 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
- Non-classic congenital adrenal hyperplasia
- 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
- 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
- Clinicopathologic and Morphologic Analysis of the Adrenal Gland in Pomeranians with Non-Illness Alopecia
- The laboratory in the multidisciplinary diagnosis of differences or disorders of sex development (DSD)
- Clinical and Imagistic Aspects in Dog’s Hyperadrenocorticism Determined by Pituitary and Adrenal Nodules with Secretory Function
- Central Diabetes Insipidus and Hypothalamic Type of Hypopituitarism Associated with Atypical Location of Rathke's Cleft Cyst
- Description and characterization of a hair coat disorder in schipperkes