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Coupling fibroblast growth factor 23 production and cleavage: iron deficiency, rickets, and kidney disease.

Wolf M, White KE.

Curr Opin Nephrol Hypertens. 2014 Jul;23(4):411-9. doi: 10.1097/01.mnh.0000447020.74593.6f. Review.


Rare bone diseases and their dental, oral, and craniofacial manifestations.

Foster BL, Ramnitz MS, Gafni RI, Burke AB, Boyce AM, Lee JS, Wright JT, Akintoye SO, Somerman MJ, Collins MT.

J Dent Res. 2014 Jul;93(7 Suppl):7S-19S. doi: 10.1177/0022034514529150. Epub 2014 Apr 3. Review.


[Rickets-like genetic diseases].

Ma HW.

Zhongguo Dang Dai Er Ke Za Zhi. 2013 Nov;15(11):923-7. Review. Chinese.


Extracellular matrix mineralization in periodontal tissues: Noncollagenous matrix proteins, enzymes, and relationship to hypophosphatasia and X-linked hypophosphatemia.

McKee MD, Hoac B, Addison WN, Barros NM, Millán JL, Chaussain C.

Periodontol 2000. 2013 Oct;63(1):102-22. doi: 10.1111/prd.12029. Review.


The changing face of hypophosphatemic disorders in the FGF-23 era.

Lee JY, Imel EA.

Pediatr Endocrinol Rev. 2013 Jun;10 Suppl 2:367-79. Review.


Osteocyte regulation of phosphate homeostasis and bone mineralization underlies the pathophysiology of the heritable disorders of rickets and osteomalacia.

Feng JQ, Clinkenbeard EL, Yuan B, White KE, Drezner MK.

Bone. 2013 Jun;54(2):213-21. doi: 10.1016/j.bone.2013.01.046. Epub 2013 Feb 9. Review.


[Fibroblast growth factor 23 mediates the phosphaturic actions of cadmium].

Kido S, Fujihara M, Nomura K, Sasaki S, Shiozaki Y, Segawa H, Tatsumi S, Miyamoto K.

Nihon Eiseigaku Zasshi. 2012;67(4):464-71. Review. Japanese.


Genetic disorders of phosphate regulation.

Gattineni J, Baum M.

Pediatr Nephrol. 2012 Sep;27(9):1477-87. doi: 10.1007/s00467-012-2103-2. Epub 2012 Feb 14. Review.


X-Linked Hypophosphatemia.

Ruppe MD.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2012 Feb 9 [updated 2014 Oct 16].


Miscellaneous non-inflammatory musculoskeletal conditions. Hyperphosphatemic familial tumoral calcinosis (FGF23, GALNT3 and αKlotho).

Farrow EG, Imel EA, White KE.

Best Pract Res Clin Rheumatol. 2011 Oct;25(5):735-47. doi: 10.1016/j.berh.2011.10.020. Review.


The role of vitamin D receptor mutations in the development of alopecia.

Malloy PJ, Feldman D.

Mol Cell Endocrinol. 2011 Dec 5;347(1-2):90-6. doi: 10.1016/j.mce.2011.05.045. Epub 2011 Jun 13. Review.


A clinician's guide to X-linked hypophosphatemia.

Carpenter TO, Imel EA, Holm IA, Jan de Beur SM, Insogna KL.

J Bone Miner Res. 2011 Jul;26(7):1381-8. doi: 10.1002/jbmr.340. Epub 2011 May 2. Review. Erratum in: J Bone Miner Res. 2015 Feb;30(2):394.

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