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Research 241–270 of 705
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- Prostaglandins: Key players in immunomodulation of the nervous system
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Prevalence, Symptomatology and Herbal Management of Polycystic Ovarian Syndrome
- Prevalence and Metabolic Characterization of Polycystic Ovary Syndrome in a Cohort of Patients Diagnosed with Spina Bifida: Study Protocol
- Pediatric adrenocortical carcinoma complicated by uric acid nephrolithiasis: a unique case report
- Exploring links between acne and metabolic syndrome: a narrative review
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- E-Poster
- Endocrinology
- Acne Vulgaris
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)
- Epithelial Stem Cells: Turning over New Leaves
- Polycystic ovary syndrome
- Sostdc1 defines the size and number of skin appendage placodes
- Histopathology of aging of the hair follicle
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Diagnosis and Management of Polycystic Ovary Syndrome in Adolescent Girls
- SOX9 in organogenesis: shared and unique transcriptional functions
- Testosterone therapy for women with low sexual desire: a position statement from the Brazilian Society of Endocrinology and Metabolism
- Epigenetic Effects of Gender-Affirming Hormone Treatment: A Pilot Study of the ESR2 Promoter’s Methylation in AFAB People
- Morphogenetic Mechanisms in the Cyclic Regeneration of Hair Follicles and Deer Antlers from Stem Cells
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Society for Endocrinology Clinical Practice Guideline for the Evaluation of Androgen Excess in Women
- Stabilization of epithelial β-catenin compromises mammary cell fate acquisition and branching morphogenesis
- Congenital Adrenal Hyperplasia
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Non-classical congenital adrenal hyperplasia: current insights into clinical implications, diagnosis and treatment