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Research 91–120 of 1000+
- The polycystic ovary syndrome: a position statement from the European Society of Endocrinology
- ВПЛИВ ВІТАМІН D-СТАТУСУ НА РІВЕНЬ ЛЕПТИНУ ТА АДИПОНЕКТИНУ В ДІТЕЙ ІЗ НАДМІРНОЮ МАСОЮ ТІЛА ТА ОЖИРІННЯМ
- Genetic basis of polycystic ovary syndrome
- Feeding the skin: The emerging role of nutritional intervention in dermatological disorders
- Endocrine systems of the skin
- Role of Nutrition in the Management of PCOS
- Polycystic ovary syndrome (PCOS) and COVID-19: an overlooked female patient population at potentially higher risk during the COVID-19 pandemic
- New Perspectives on Nutraceutical Insulin Sensitizing Agents in the Treatment of Psoriasis and Other Dermatological Diseases
- PSAT217 Estrogen Deficiency as a Cause of Decreased 1- alpha - hydroxylase Activity
- Hair Loss in Systemic Disease
- Impact of Reducing Obesity in PCOS: Methods and Treatment Outcomes
- Lean Women with Polycystic Ovary Syndrome
- Optimizing Nutrition for PCOS Management: A Comprehensive Guide
- Endocrine control of benign prostatic hyperplasia
- Polycystic ovary syndrome and infertility: an update
- The clinical spectrum of parathyroid disease
- Vitamin Deficiency, Dependency, and Toxicity
- Effect of a low insulinemic diet on clinical, biochemical and metabolic outcomes in women with polycystic ovary syndrome (PCOS)
- Noncalcemic actions of 1,25-dihydroxyvitamin D3 and clinical applications
- Calcium and Vitamin D Signaling in the Epidermal Response to Wounding
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Vitamin D and the skin
- Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- Hereditary vitamin D rickets: a case series in a family
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary vitamin D-resistant rickets resulting from a novel mutation
- Vitamin D and the skin: Physiology and pathophysiology