
pmid: 1102648
Since the introduction of irradiated ergosterol into our food supply, nutritional vitamin D-deficiency rickets has become an uncommon disease. However, skeletal disorders due to abnormalities of vitamin D function still occur. These disorders can now be classified more exactly into two groups: those in which there is a deficiency of the active metabolite of vitamin D, 1,25-dihydroxyvitamin D, and those in which there is an abnormality of renal tubular function resulting in renal hypophosphatemia despite normal vitamin D metabolism. The various entities of these two groups are described and the theoretical basis of their treatment given.
Hyperparathyroidism, Infant, Fanconi Syndrome, Vitamin D Deficiency, Phosphates, Glycosuria, Osteomalacia, Dihydrotachysterol, Humans, Hyperparathyroidism, Secondary, Renal Aminoacidurias, Vitamin D, Hypophosphatemia, Familial, Rickets
Hyperparathyroidism, Infant, Fanconi Syndrome, Vitamin D Deficiency, Phosphates, Glycosuria, Osteomalacia, Dihydrotachysterol, Humans, Hyperparathyroidism, Secondary, Renal Aminoacidurias, Vitamin D, Hypophosphatemia, Familial, Rickets
| citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 28 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
