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Research 31–60 of 1000+
- Challenges in diagnosis and treatment of Cushing disease in a 12-year-old boy
- SUN-174 Giant Bilateral Myelolipomas in a Patient with Congenital Adrenal Hyperplasia
- A Case of the Cons: How Contraception Confused Congenital Adrenal Hyperplasia for Conn
- Role of the ACTH/MC2R System in the Hair Cycle in Mice
- ACTH as first line treatment for acute calcium pyrophosphate crystal arthritis in 14 hospitalized patients
- CYP21A2 Genotypes do not Predict the Severity of Hyperandrogenic Manifestations in the Nonclassical Form of Congenital Adrenal Hyperplasia
- Congenital Adrenal Hyperplasia
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- Melanocortin receptor type 2 (MC2R, ACTH receptor) expression in patients with alopecia areata
- An implication for post-transcriptional control: Reciprocal changes of melanocortin receptor type 2 mRNA and protein expression in alopecia areata
- Screening for 21-hydroxylase–deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*
- Cutaneous manifestations of endocrine-metabolic disease and nutritional deficiency in the elderly
- 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
- Clinical analysis of 78 patients with non-classical 21-hydroxylase deficiency
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Secondary Adrenal Insufficiency : A Case Report
- An Update of Congenital Adrenal Hyperplasia
- A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Changes of androgens levels in menopausal women
- CYP21A2 Mutations in Women with Polycystic Ovary Syndrome (PCOS)
- May AMH levels distinguish LOCAH from PCOS among hirsute women?
- An X-traordinary stroke
- Nonclassic Congenital Adrenal Hyperplasia: An Overview