Subject Areas on Research
- A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia: evidence that the disorder is not a distinct entity from X-linked hypophosphatemic rickets.
- Azotemic renal osteodystrophy.
- Coupling fibroblast growth factor 23 production and cleavage: iron deficiency, rickets, and kidney disease.
- Craniosynostosis and rickets.
- Healing of bone disease in X-linked hypophosphatemic rickets/osteomalacia. Induction and maintenance with phosphorus and calcitriol.
- Human vitamin D receptor mutations: identification of molecular defects in hypocalcemic vitamin D resistant rickets.
- Hypophosphatemic rickets in opsismodysplasia.
- Newer knowledge of vitamin D and its metabolites in health and disease.
- Normal calcitonin stimulation of serum calcitriol in patients with X-linked hypophosphatemic rickets.
- Parathyroid hormone effects on serum 1,25-dihydroxyvitamin D levels in patients with X-linked hypophosphatemic rickets: evidence for abnormal 25-hydroxyvitamin D-1-hydroxylase activity.
- The concurrence of hypoparathyroidism provides new insights to the pathophysiology of X-linked hypophosphatemic rickets.
- The efficacy of vitamin D2 and oral phosphorus therapy in X-linked hypophosphatemic rickets and osteomalacia.
- X-linked hypophosphatemic rickets without "rickets".
Keywords of People
- Adkins, Deanna Wilson, Associate Professor of Pediatrics, Pediatrics, Endocrinology