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Research 61–90 of 815
- A Model for Predicting Polycystic Ovary Syndrome Using Serum AMH, Menstrual Cycle Length, Body Mass Index and Serum Androstenedione in Chinese Reproductive Aged Population: A Retrospective Cohort Study
- E-Poster
- Alcohol and Prostate Cancer: Time to Draw Conclusions
- Leucine-Rich Repeat-Containing G-Protein-Coupled Receptors as Markers of Adult Stem Cells
- Inherited Epidermolysis Bullosa: A Clinical Case
- An Update of Congenital Adrenal Hyperplasia
- Collagen-Heparin-FGF2-VEGF Scaffolds Induce a Regenerative Gene Expression Profile in a Fetal Sheep Wound Model
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.
- Hyperandrogenism in polycystic ovary syndrome and adrenal hyperplasia: finding differences to make a specific diagnosis
- The urine as a diagnostic key for a homozygous EGFR mutation
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Cardiometabolic and neuroimaging correlates of cognitive function in polycystic ovary syndrome
- The Impact of Pregnancy Specific Distress on Hair Loss in Women in Their Third Trimester
- Functional Ingredient Mapping in PCOS Formulations: Hormonal Excess
- EFFECT OF THYROID DYSFUNCTION ON BODY MASS INDEX AND HORMONAL IMBALANCE IN WOMEN HAVING POLYCYSTIC OVARIAN SYNDROME
- SUMMARIES OF PAPERS
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Highlights from the 68th Annual Meeting of the Society of Investigative Dermatology
- Standards of Care for the Health of Transsexual, Transgender, and Gender-Nonconforming People, Version 7
- Polycystic ovary syndrome
- Endocrine Treatment of Transsexual Persons:An Endocrine Society Clinical Practice Guideline
- Use of chemotherapy during human pregnancy
- Developmental origin of polycystic ovary syndrome - a hypothesis
- Evidence-Based and Potential Benefits of Metformin in the Polycystic Ovary Syndrome: A Comprehensive Review
- The Rotterdam Study: 2016 objectives and design update