Hypophosphatemic Rickets
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference138 articles.
1. A genetic study of familial hypophosphatemia and vitamin D resistant rickets with a review of the literature;Winters;Medicine (Baltimore),1958
2. Disorders of phosphorus metabolism;Haffner,2016
3. Mutational analysis of PHEX, FGF23, DMP1, SLC34A3 and CLCN5 in patients with hypophosphatemic rickets;Beck-Nielsen;J Hum Genet,2012
4. A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP Consortium;Consortium;Nat Genet,1995
5. Genetic disorders of phosphate regulation;Gattineni;Pediatr Nephrol,2012
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1. Disorders of Calcium and Phosphorus Metabolism;Avery's Diseases of the Newborn;2024
2. X-linked hypophosphatemia in 4 generations due to an exon 13–15 duplication in PHEX, in the absence of the c.*231A>G variant;Bone;2023-07
3. Tubulopatías;Medicine - Programa de Formación Médica Continuada Acreditado;2023-06
4. Mineral Metabolism in Children: Interrelation between Vitamin D and FGF23;International Journal of Molecular Sciences;2023-04-03
5. Dental manifestations and treatment of hypophosphatemic rickets: A case report and review of literature;BDJ Open;2023-01-30
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