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Research 61–90 of 542
- Polyglandular Syndrome Type 1 Complicated with Dilated Cardiomyopathy: A Case Report
- Nonfebrile Seizures in Pediatrics: Key Points to Remember
- Care Considerations and Management of Transgender Individuals After Kidney Transplantation: A Single Institution Experience and Literature Review
- G338(P) Dermatological manifestations in children with chronic kidney disease in a tertiary care center: a case-control study
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- 503 Use of low-dose spironolactone in female pattern hair loss in a specialty alopecia clinic
- Parathyroid adenoma with coeliac disease: primary or quaternary hyperparathyroidism?
- Enhancing 1α-Hydroxylase Activity with the 25-Hydroxyvitamin D-1α-Hydroxylase Gene in Cultured Human Keratinocytes and Mouse Skin
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- 451 Spironolactone for treatment of concomitant female pattern hair loss in scarring alopecia patients
- The parathyroid hormone-related protein as a regulator of normal tissue functions
- Mechanism of Vitamin D Receptor Action
- Nongenomic effects of 1α,25-dihydroxyvitamin D 3 on cartilage formation deduced from comparisons between Cyp27b1 and Vdr knockout mice
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- Spironolactone
- ADVANCES IN PSORIASIS THERAPY
- Topical absorption and systemic toxicity
- Dermatological drugs, topical agents, and cosmetics
- Quality of Calcium Food Supplements: Evaluation Compared to Manufacturers’ Declarations
- Case of Waldenstrom Macroglobulinaemia Mimicking Multiple Myeloma: A Diagnostic Challenge
- Congenital Adrenal Hyperplasia
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Diuretics
- SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Spironolactone
- Case of Cronkhite Canada Syndrome - A Non-Inherited Gastrointestinal Polyposis Syndrome
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Endocrine-skin interactions
- Mouse models with a disrupted PTHrP gene or a disrupted PTH gene (PTH−/− mice)