Hypophosphatemic Rickets

Overview

Journal Rev Endocr Metab Disord

Publisher Springer

Specialty Endocrinology

Date 2001 Nov 14

PMID 11705322

Citations 4

Authors

L A DiMeglio

M J Econs

Affiliations

Soon will be listed here.

Citing Articles

Hereditary hypophosphatemic rickets with hypercalciuria: pathophysiology, clinical presentation, diagnosis and therapy.

Bergwitz C, Miyamoto K Pflugers Arch. 2018; 471(1):149-163.

PMID: 30109410 DOI: 10.1007/s00424-018-2184-2.

FGF23 and syndromes of abnormal renal phosphate handling.

Bergwitz C, Juppner H Adv Exp Med Biol. 2012; 728:41-64.

PMID: 22396161 PMC: 5234086. DOI: 10.1007/978-1-4614-0887-1_3.

Disorders of phosphate homeostasis and tissue mineralisation.

Bergwitz C, Juppner H Endocr Dev. 2009; 16:133-56.

PMID: 19494665 PMC: 3810012. DOI: 10.1159/000223693.

An ethyl-nitrosourea-induced point mutation in phex causes exon skipping, x-linked hypophosphatemia, and rickets.

Carpinelli M, Wicks I, Sims N, ODonnell K, Hanzinikolas K, Burt R Am J Pathol. 2002; 161(5):1925-33.

PMID: 12414538 PMC: 1850771. DOI: 10.1016/S0002-9440(10)64468-9.

References

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