Evidence suggesting hyperoxaluria as a cause of nephrocalcinosis in phosphate-treated hypophosphataemic rickets
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference23 articles.
1. Clinical experience with 41 typical familial hypophosphatemic patients and 2 atypical nonfamilial cases;Stickler;Mayo Clin Proc,1970
2. Familial forms of vitamin D-resistant rickets revisited. X-linked hypophosphatemia and autosomal recessive vitamin D dependency;Fraser;Am J Clin Nutr,1976
3. Hereditary hypophosphatemic rickets with hypercalciuria;Tieder;N Engl J Med,1985
4. Impaired phosphorus conservation and 1,25 dihydroxyvitamin D generation during phosphorus deprivation in familial hypophosphatemic rickets;Isogna;J Clin Invest,1983
5. Serum 1,25-dihydroxyvitamin D levels in subjects with X-linked hypophosphatemic rickets and osteomalacia;Lyles;Calcif Tissue Int,1982
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