Hypophosphatemic nonrachitic bone disease: An entity distinct from X‐linked hypophosphatemia in the renal defect, bone involvement, and inheritance
- 1 January 1977
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 1 (1), 101-117
- https://doi.org/10.1002/ajmg.1320010111
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Familial forms of vitamin D-resistant rickets revisited. X-linked hypophosphatemia and autosomal recessive vitamin D dependencyThe American Journal of Clinical Nutrition, 1976
- X-linked hypophosphataemia and autosomal recessive vitamin D dependency: Models for the resolution of vitamin D refractory ricketsPublished by Springer Science and Business Media LLC ,1976
- Metabolic forms of rickets (and osteomalacia)Published by Springer Science and Business Media LLC ,1976
- Actions of 1,25-Dihydroxycholecalciferol in Patients with Hypophosphatemic, Vitamin-D-Resistant RicketsNew England Journal of Medicine, 1973
- Use of Phosphate and Vitamin D to Prevent Dwarfism and Rickets in X-Linked HypophosphatemiaNew England Journal of Medicine, 1972
- Loss of a Parathyroid Hormone-Sensitive Component of Phosphate Transport in X-Linked HypophosphatemiaScience, 1972
- COMPETITIVE PROTEIN-BINDING RADIOASSAY FOR 25-HYDROXYCHOLECALCIFEROL1Journal of Clinical Endocrinology & Metabolism, 1971
- Radioimmunoassay of human parathyroid hormone in serumJCI Insight, 1971
- Evaluation of Theoretical Renal Phosphorus Threshold as an Index of Renal Phosphorus HandlingClinical Science, 1970
- A Protein Binding Assay for Adenosine 3′:5′-Cyclic MonophosphateProceedings of the National Academy of Sciences of the United States of America, 1970