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Research 61–90 of 1000+
- Congenital adrenal hyperplasia with polycystic ovarian disease: A rare cause of hirsutism
- Isotretinoin-unresponsive acne as a sign of a congenital disorder: a case of 21-hydroxylase deficiency
- Management Approaches to Congenital Adrenal Hyperplasia in Adolescents and Adults; Latest Therapeutic Developments
- A Case of the Cons: How Contraception Confused Congenital Adrenal Hyperplasia for Conn
- Adrenal 21-hydroxylase gene mutations in Slovenian hyperandrogenic women: evaluation of corticotrophin stimulation and HLA polymorphisms in screening for carrier status
- Defects in Androgen Biosynthesis Causing 46,XY Disorders of Sexual Development
- Secondary Amenorrhea and Clinical Hyperandrogenism in a 34-Year-Old Female: Polycystic Ovary Syndrome or Not?
- Epicardial Fat Thickness in Children with Classic Congenital Adrenal Hyperplasia
- Epicardial fat thickness in children with classic congenital adrenal hyperplasia
- Expression and roles of steroidogenic acute regulatory (StAR) protein in ‘non-classical’, extra-adrenal and extra-gonadal cells and tissues
- An Adult With Hair Loss! a Rare Case of Non-Classical 3β Hydroxysteroid Dehydrogenase (3β HSD) Deficiency
- Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- Methods of hair loss evaluation in patients with endocrine disorders.
- INCIDENCE OF VIRILISATION IN SEX CORD STROMAL TUMOURS OF OVARY, A 5- YEAR EXPERIENCE IN A TERTIARY CARE GYNAECOLOGICAL CENTRE
- Approach to androgen excess in women: Clinical and biochemical insights
- Mister XX
- Prematüre Pubarş Olgularının Değerlendirilmesi: Tek Merkez Deneyimi
- Testicular Steroidogenesis
- Voice changes in reproductive disorders, thyroid disorders and diabetes: a review
- Hyperadrenocorticism in Ferrets
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- Nonclassic adrenal hyperplasia
- 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
- Screening for 21-hydroxylase–deficient nonclassic adrenal hyperplasia among hyperandrogenic women: a prospective study
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- Measuring steroids in hair opens up possibilities to identify congenital adrenal hyperplasia in developing countries
- Severe impact of late diagnosis of congenital adrenal hyperplasia on gender identity, sexual orientation and function: case report and review of the literature