X-Linked Hypophosphataemic Rickets and Growth

Author:

Santos Rodríguez FernandoORCID

Funder

Kyowa Kirin

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),General Medicine

Reference29 articles.

1. Ramussen H, Anast C. Familial hypophosphatemic rickets and vitamin D-dependent rickets. In: Wyngaarden JB, Fredericson DS, Goldstain JL, Brrown MS, editors. The metabolic basis of inherit disease. New York: McGraw-Hill; 1983. p. 1743–73.

2. Dixon PH, Christie PT, Wooding C, et al. Mutational analysis of PHEX gene in X-linked hypophosphatemia. J Clin Endocrinol Metab. 1998;83(10):3615–23.

3. Tenenhouse HS. X-linked hypophosphataemia: a homologous disorder in humans and mice. Nephrol Dial Transplant. 1999;14(2):333–41.

4. Bastepe M, Juppner H. Inherited hypophosphatemic disorders in children and the evolving mechanisms of phosphate regulation. Rev Endocr Metab Disord. 2008;9(2):171–80.

5. Rowe PS. Regulation of bone-renal mineral and energy metabolism: the PHEX, FGF23, DMP1, MEPE ASARM pathway. Crit Rev Eukaryot Gene Expr. 2012;22(1):61–86.

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