(Q37411821)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18996815%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

title

A patient with hypophosphatemia, a femoral fracture, and recurrent kidney stones: report of a novel mutation in SLC34A3 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18996815%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

1 reference

1 reference

5

1 reference

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26 December 2019

author name string

Kathleen Page

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18996815%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

Clemens Bergwitz

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18996815%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

Graciana Jaureguiberry

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18996815%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

Chittari V Harinarayan

4

1 reference

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26 December 2019

publication date

1 October 2008

1 reference

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26 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18996815%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

volume

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18996815%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

issue

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18996815%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

page(s)

869-874

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18996815%20AND%20SRC:MED&resulttype=core&format=json

Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3.

26 December 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2773288

SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2773288

Nomogram for derivation of renal threshold phosphate concentration

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2773288

Osteomalacia in hereditary hypophosphatemic rickets with hypercalciuria: a correlative clinical-histomorphometric study

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2773288

Oxalate absorption and postprandial urine supersaturation in an experimental human model of absorptive hypercalciuria.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2773288

Increased circulating concentrations of parathyroid hormone in healthy, young women consuming a protein-restricted diet

2 September 2018

1 reference

12 December 2020

Intronic deletions in the SLC34A3 gene cause hereditary hypophosphatemic rickets with hypercalciuria

1 reference

12 December 2020

Bone resorption stimulated by elevated serum 1,25-(OH)2-vitamin D concentrations in healthy men

1 reference

12 December 2020

Hereditary hypophosphatemic rickets with hypercalciuria

1 reference

12 December 2020

Hyperoxaluria is not a cause of nephrocalcinosis in phosphate-treated patients with hereditary hypophosphatemic rickets

1 reference

12 December 2020

Identifiers

DOI

10.4158/EP.14.7.869

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18996815%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

1 reference

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26 December 2019

PubMed publication ID

18996815

1 reference