(Q53537704)

15 May 2018

title

Growth hormone improves growth rate and preserves renal function in Dent disease. (English)

1 reference

15 May 2018

author name string

Sharone Sheffer-Babila

series ordinal

1

1 reference

15 May 2018

Manju Chandra

series ordinal

2

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15 May 2018

Phyllis W Speiser

series ordinal

3

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15 May 2018

publication date

1 March 2008

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15 May 2018

Journal of Pediatric Endocrinology and Metabolism

published in

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15 May 2018

volume

21

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15 May 2018

issue

3

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15 May 2018

page(s)

279-286

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15 May 2018

Intra-renal and subcellular distribution of the human chloride channel, CLC-5, reveals a pathophysiological basis for Dent's disease

cites work

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2008.21.3.279

Novel truncating mutations in the ClC-5 chloride channel gene in patients with Dent's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2008.21.3.279

Dent's disease: can we slow its progression?

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2008.21.3.279

Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5)

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2008.21.3.279

Pathogenesis of Dent's disease and related syndromes of X-linked nephrolithiasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2008.21.3.279

ClC-5 Cl- -channel disruption impairs endocytosis in a mouse model for Dent's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2008.21.3.279

Modeling study of human renal chloride channel (hCLC-5) mutations suggests a structural-functional relationship.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2008.21.3.279

The GEF1 gene of Saccharomyces cerevisiae encodes an integral membrane protein; mutations in which have effects on respiration and iron-limited growth.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2008.21.3.279

A common molecular basis for three inherited kidney stone diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2008.21.3.279

Update on X-linked hypogammaglobulinemia with isolated growth hormone deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2008.21.3.279

Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2008.21.3.279

Growth factors and renal regulation of phosphate transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2008.21.3.279

10.1515/JPEM.2008.21.3.279

21 January 2018

Identifiers

DOI

1 reference

15 May 2018

PubMed ID

18540256

1 reference

15 May 2018