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Items: 1 to 20 of 113

1.

Hypophosphatemic rickets: A case of recurrent pathological fractures.

Baidya A, Chowdhury S, Mukhopadhyay S, Ghosh S.

Indian J Endocrinol Metab. 2012 Dec;16(Suppl 2):S402-4. doi: 10.4103/2230-8210.104108.

2.

The concurrence of hypoparathyroidism provides new insights to the pathophysiology of X-linked hypophosphatemic rickets.

Lyles KW, Burkes EJ Jr, McNamara CR, Harrelson JM, Pickett JP, Drezner MK.

J Clin Endocrinol Metab. 1985 Apr;60(4):711-7.

PMID:
4038714
3.
4.

Healing of bone disease in X-linked hypophosphatemic rickets/osteomalacia. Induction and maintenance with phosphorus and calcitriol.

Harrell RM, Lyles KW, Harrelson JM, Friedman NE, Drezner MK.

J Clin Invest. 1985 Jun;75(6):1858-68.

5.

A pediatric hypophosphatemic rickets on MRI, 99mTc-MDP bone scan and 18F-FDG PET/CT.

Xu C, Ma C, Bai Y.

Hell J Nucl Med. 2017 Jan-Apr;20(1):93-96. doi: 10.1967/s002449910515. Epub 2017 Mar 20.

6.
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8.

Tumor-induced osteomalacia.

Florenzano P, Gafni RI, Collins MT.

Bone Rep. 2017 Sep 20;7:90-97. doi: 10.1016/j.bonr.2017.09.002. eCollection 2017 Dec.

9.

Hereditary hypophosphatemic rickets with hypercalciuria: case report.

Areses-Trapote R, López-García JA, Ubetagoyena-Arrieta M, Eizaguirre A, Sáez-Villaverde R.

Nefrologia. 2012 Jul 17;32(4):529-34. doi: 10.3265/Nefrologia.pre2012.Apr.11321. English, Spanish.

10.

[Changes in mineral metabolism in stage 3, 4, and 5 chronic kidney disease (not on dialysis)].

Lorenzo Sellares V, Torregrosa V.

Nefrologia. 2008;28 Suppl 3:67-78. Spanish.

11.

Rare tubulopathy - primary hypophosphatemic rickets (case report).

Tsanava M, Abuladze T, Zenaishvili B, Kvaratskhelia E, Pagava K.

Georgian Med News. 2011 Apr;(193):93-7.

PMID:
21617285
12.

Levels and dynamic changes of serum fibroblast growth factor 23 in hypophosphatemic rickets/osteomalacia.

Xia WB, Jiang Y, Li M, Xing XP, Wang O, Hu YY, Zhang HB, Liu HC, Meng XW, Zhou XY.

Chin Med J (Engl). 2010 May 5;123(9):1158-62.

PMID:
20529556
13.

Resolution of severe, adolescent-onset hypophosphatemic rickets following resection of an FGF-23-producing tumour of the distal ulna.

Ward LM, Rauch F, White KE, Filler G, Matzinger MA, Letts M, Travers R, Econs MJ, Glorieux FH.

Bone. 2004 May;34(5):905-11.

PMID:
15121023
14.

X-linked hypophosphatemic rickets: case report.

Radlović V, Smoljanić Z, Radlović N, Leković Z, Ristić D, Ducić S, Pavićević P.

Srp Arh Celok Lek. 2014 Jan-Feb;142(1-2):75-8.

15.

A compound heterozygous mutation in SLC34A3 causes hereditary hypophosphatemic rickets with hypercalciuria in a Chinese patient.

Chi Y, Zhao Z, He X, Sun Y, Jiang Y, Li M, Wang O, Xing X, Sun AY, Zhou X, Meng X, Xia W.

Bone. 2014 Feb;59:114-21. doi: 10.1016/j.bone.2013.11.008. Epub 2013 Nov 16.

PMID:
24246249
16.

[Different forms of clinical presentation of an autosomal dominant hypophosphatemic rickets caused by a FGF23 mutation in one family].

Negri AL, Negrotti T, Alonso G, Pasqualini T.

Medicina (B Aires). 2004;64(2):103-6. Spanish.

PMID:
15628294
17.

Hypophosphatemic rickets and osteomalacia.

de Menezes Filho H, de Castro LC, Damiani D.

Arq Bras Endocrinol Metabol. 2006 Aug;50(4):802-13. Review.

18.

Metabolic studies in a patient with idiopathic hypophosphatemic osteomalacia.

Weiss M, Schechter P, Bab I, Mekhmandarov S, Bank H, Eisenstein Z.

Isr J Med Sci. 1988 Jan;24(1):46-50.

PMID:
3346150
19.

Pseudo-(tumor-induced) rickets.

Whyte MP, Podgornik MN, Wollberg VA, Eddy MC, McAlister WH.

J Bone Miner Res. 2001 Aug;16(8):1564-71.

20.

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