Iron replacement ameliorates hypophosphatemia in autosomal dominant hypophosphatemic rickets: A review of the role of iron
Author:
Publisher
Elsevier BV
Subject
Histology,Physiology,Endocrinology, Diabetes and Metabolism
Reference32 articles.
1. Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23;ADHR Consortium;Nat. Genet.,2000
2. Autosomal dominant hypophosphatemic rickets/osteomalacia: clinical characterization of a novel renal phosphate-wasting disorder;Econs;J. Clin. Endocrinol. Metab.,1997
3. The autosomal dominant hypophosphatemic rickets R176Q mutation in fibroblast growth factor 23 resists proteolytic cleavage and enhances in vivo biological potency;Bai;J. Biol. Chem.,2003
4. Fibroblast growth factor 23 reduces expression of type IIa Na+/Pi co-transporter by signaling through a receptor functionally distinct from the known FGFRs in opossum kidney cells;Yan;Genes Cells,2005
5. Fibroblast growth factor 23 impairs phosphorus and vitamin D metabolism in vivo and suppresses 25-hydroxyvitamin D-1alpha-hydroxylase expression in vitro;Perwad;Am. J. Physiol. Renal. Physiol.,2007
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1. A Novel Pathogenic Variant in <i>Fibroblast Growth Factor 23</i> outside the Furin-Recognizing RXXR Motif in an Autosomal Dominant Hypophosphatemic Rickets Patient;Hormone Research in Paediatrics;2024-03-15
2. X-linked hypophosphatemia caused by a deep intronic variant in PHEX identified by PCR-based RNA analysis of urine-derived cells;Bone;2023-11
3. High-Dose Intravenous Iron with Either Ferric Carboxymaltose or Ferric Derisomaltose: A Benefit-Risk Assessment;Drug Safety;2022-09-06
4. Iron deficiency plays essential roles in the trigger, treatment, and prognosis of autosomal dominant hypophosphatemic rickets;Osteoporosis International;2020-09-30
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