Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia-Reference-Cited by-同舟云学术

Clinical practice recommendations for the diagnosis and management of X-linked hypophosphataemia

Published:2019-05-08 Issue:7 Volume:15 Page:435-455
ISSN:1759-5061
Container-title:Nature Reviews Nephrology
language:en
Short-container-title:Nat Rev Nephrol

Author:

Haffner Dieter^ORCID,Emma Francesco,Eastwood Deborah M.,Duplan Martin Biosse,Bacchetta Justine,Schnabel Dirk,Wicart Philippe,Bockenhauer Detlef^ORCID,Santos Fernando,Levtchenko Elena,Harvengt Pol,Kirchhoff Martha,Di Rocco Federico,Chaussain Catherine,Brandi Maria Louisa,Savendahl Lars^ORCID,Briot Karine,Kamenicky Peter,Rejnmark Lars^ORCID,Linglart Agnès

Publisher

Springer Science and Business Media LLC

Subject

Nephrology

Link

http://www.nature.com/articles/s41581-019-0152-5.pdf

Reference196 articles.

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2. Endo, I. et al. Nationwide survey of fibroblast growth factor 23 (FGF23)-related hypophosphatemic diseases in Japan: prevalence, biochemical data and treatment. Endocr. J. 62, 811–816 (2015).

3. Rafaelsen, S., Johansson, S., Ræder, H. & Bjerknes, R. Hereditary hypophosphatemia in Norway: a retrospective population-based study of genotypes, phenotypes, and treatment complications. Eur. J. Endocrinol. 174, 125–136 (2016).

4. Liu, S. et al. Pathogenic role of Fgf23 in Hyp mice. Am. J. Physiol. Endocrinol. Metab. 291, E38–E49 (2006).

5. Feng, J. Q., Clinkenbeard, E. L., Yuan, B., White, K. E. & Drezner, M. K. Osteocyte regulation of phosphate homeostasis and bone mineralization underlies the pathophysiology of the heritable disorders of rickets and osteomalacia. Bone 54, 213–221 (2013).

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