Hypophosphataemic Rickets: Similar Phenotype of Different Diseases-Reference-Cited by-同舟云学术

Hypophosphataemic Rickets: Similar Phenotype of Different Diseases

Published:2020-03-31 Issue:S2 Volume:37 Page:80-88
ISSN:0741-238X
Container-title:Advances in Therapy
language:en
Short-container-title:Adv Ther

Author:

de la Cerda-Ojeda Francisco^ORCID,González-Rodríguez Juan D.^ORCID,Madariaga Leire^ORCID,Martínez-Díaz-Guerra Guillermo^ORCID,Matoses-Ruipérez María L.^ORCID

Funder

Kyowa Kirin

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s12325-019-01182-3.pdf

Reference35 articles.

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2. Kanbay M, Vervloet M, Cozzolino M, et al. Novel faces of fibroblast growth factor 23 (FGF23): iron deficiency, inflammation, insulin resistance, left ventricular hypertrophy, proteinuria and acute kidney injury. Calcif Tissue Int. 2017;100:217–28.

3. Michalus I, Rusinska A. Rare, genetically conditioned forms of rickets: differential diagnosis and advances in diagnostics and treatment. Clin Genet. 2018;94:103–14.

4. Carpenter TO. The expanding family of hypophosphatemic syndromes. J Bone Miner Metab. 2012;30:1–9.

5. Beck-Nielsen SS, Brusgaard K, Rasmussen LM, et al. Phenotype presentation of hypophosphatemic rickets in adults. Calcif Tissue Int. 2010;87:108–19.

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1. Safety and Efficacy of Burosumab in Pediatric Patients With X-Linked Hypophosphatemia: A Phase 3/4 Open-Label Trial;Journal of the Endocrine Society;2022-02-11

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