Disease: Pseudohermaphroditism male with gynecomastia
- <em>MYRF</em>-Related Cardiac Urogenital Syndrome
- 17-β-hydroxysteroid dehydrogenase type 3 deficiency in three adult Iranian siblings
- 46 XY disorder of sex development (DSD) due to 5 alpha (SRD5A2) deficiency - Experience from a multidisciplinary Pediatric Gender Clinic
- 46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parameters
- 46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin
- A case of Kallmann syndrome associated to a novel missense mutation of the FGFR1 gene
- A case of mild partial androgen insensitivity syndrome in a juvenile boy
- A novel nonsense mutation in HSD17B3 gene in a Tunisian patient with sexual ambiguity
- A rare case of a 34-year-old patient diagnosed late with Kallmann syndrome: case report
- Aromatase deficiency in transplanted bone marrow cells improves vertebral trabecular bone quantity, connectivity, and mineralization and decreases cortical porosity in murine bone marrow transplant recipients
- Case of newly diagnosed bilateral anorchia in a 42-year-old male patient
- Clinical, Biochemical, and Molecular Characterization of Indian Children with Clinically Suspected Androgen Insensitivity Syndrome
- Clinical, Hormonal, Genetic, and Molecular Characteristics in Androgen Insensitivity Syndrome in an Asian Indian Cohort from a Single Centre in Western India
- Congenital Adrenal Hyperplasia with Combined 21-hydroxylase deficiency and 17alpha-hydroxylase/17,20-lyase deficiency: An undervirilized male
- Cushing's syndrome diagnosed incidentally on CT imaging
- Disorder of Sex Development Due to 17-Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency: A Case Report and Review of 70 Different <em>HSD17B3</em> Mutations Reported in 239 Patients
- Effect of Essential Oil Components on the Activity of Steroidogenic Cytochrome P450
- Four novel mutations identification in 17 beta-hydroxysteroid dehydrogenase-3 deficiency and our clinical experience: possible benefits of early treatment
- Four novel mutations in the androgen receptor gene from Vietnamese patients with androgen insensitivity syndrome
- Gender identity disorder (GID) in adolescents and adults with differences of sex development (DSD): A systematic review and meta-analysis
- Hypergonadotropic hypogonadism and chromosomal aberrations: clinical heterogeneity and implications on the health of elderly men, case series
- Hypogonadotropic hypogonadism with Zinner syndrome: a coincidence or a consequence?
- Initial assessment of a child with suspected disorder of sex development
- Klinefelter syndrome: The characterization of the clinical and sociological features of 51 patients
- Long-term consequences of androgen insensitivity syndrome
- Male pseudohermaphroditism due to testicular 17 -hydroxysteroid dehydrogenase deficiency
- Malignant interstitial cell carcinoma of the testis: report of two cases with steroid synthetic profiles, response to therapy, and review of the literature
- Multiparameter Investigation of a 46,XX/46,XY Tetragametic Chimeric Phenotypical Male Patient with Bilateral Scrotal Ovotestes and Ovulatory Activity
- Ovotesticular disorder of sex development in a 46 XY adolescent: a rare case report with review of the literature
- Pitfalls in hormonal diagnosis of 17-beta hydroxysteroid dehydrogenase III deficiency
- Predicting puberty in partial androgen insensitivity syndrome: Use of clinical and functional androgen receptor indices
- Primary amenorrhea in a young Polish woman with complete androgen insensitivity syndrome and Sertoli-Leydig cell tumor: identification of a new androgen receptor gene mutation and evidence of aromatase hyperactivity and apoptosis dysregulation within the
- Pubertal Development in 17Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency
- Screening for mutations in 17β-hydroxysteroid dehydrogenase and androgen receptor in women presenting with partially virilised 46,XY disorders of sex development
- Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene
- Sex Reversal Syndrome (SRS): A Case of SRY-Positive 46,XX Testicular Disorder
- Spectrum of external genital anomalies in disorders of Sex Development at Children Hospital & Institute of Child Health, Lahore, Pakistan
- Structural analysis of the impact of a novel androgen receptor gene mutation in two adult patients with mild androgen insensitivity syndrome
- The First Case Report of 47,XXY/46,XX/46,XY Mosaic Klinefelter Syndrome Patient With Mixed Connective Tissue Disorder
- The Klinefelter Syndrome and Testicular Sperm Retrieval Outcomes