Disorders of Phosphate Metabolism: Autosomal Dominant Hypophosphatemic Rickets, Tumor Induced Osteomalacia, Fibrous Dysplasia, and the Pathophysiological Relevance of FGF23

Author:

ECONS MICHAEL J.

Publisher

Elsevier

Reference38 articles.

1. Familial hypophosphatemic rickets showing autosomal dominant inheritance;Bianchine;Birth Defects: Original Article Series,1971

2. Autosomal dominant hypophosphatemic rickets/osteomalacia: clinical characterization of a novel renal phosphate wasting disorder;Econs;J Clin Endocrinol Metab,1997

3. Autosomal dominant hypophosphatemic rickets is linked to chromosome 12p 13;Econs;J Clin Invest,1997

4. Autosomal dominant hypophosphatemic rickets is associated with mutations in FGF23;The ADHR Consortium;Nature Genetics,2000

5. Hypophosphatemic nonrachitic bone disease: an entity distinct from X-linked hypophosphatemia in the renal defect, bone involvement, and inheritance;Scriver;American Journal of Medical Genetics,1977

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1. Vitamin D: sources, physiological role, biokinetics, deficiency, therapeutic use, toxicity, and overview of analytical methods for detection of vitamin D and its metabolites;Critical Reviews in Clinical Laboratory Sciences;2022-05-16

2. Vitamin D and Phosphate Interactions in Health and Disease;Advances in Experimental Medicine and Biology;2022

3. Phosphorus;Present Knowledge in Nutrition;2012-06-18

4. Vitamin D Disorders;Genetic Diagnosis of Endocrine Disorders;2010

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