(Q34417406)

2 August 2017

0 references

A case of Bartter syndrome type I with atypical presentations (English)

1 reference

2 August 2017

Eun Hye Lee

1

1 reference

2 August 2017

Ju Sun Heo

2

1 reference

2 August 2017

Hyun Kyung Lee

3

1 reference

2 August 2017

Kyung Hee Han

4

1 reference

2 August 2017

Hee Gyung Kang

5

1 reference

2 August 2017

Il Soo Ha

6

1 reference

2 August 2017

Yong Choi

7

1 reference

2 August 2017

Hae Il Cheong

8

1 reference

2 August 2017

publication date

31 August 2010

1 reference

Korean journal of pediatrics

2 August 2017

published in

1 reference

2 August 2017

volume

53

1 reference

2 August 2017

issue

8

1 reference

2 August 2017

page(s)

809-813

1 reference

Creative Commons Attribution-NonCommercial 3.0 Unported

2 August 2017

copyright license

start time

1 January 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Thick ascending limb: the Na(+):K (+):2Cl (-) co-transporter, NKCC2, and the calcium-sensing receptor, CaSR

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004498

Regulation of cation transport in the distal nephron by mechanical forces

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004498

Salt handling in the distal nephron: lessons learned from inherited human disorders.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004498

Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis. A new syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004498

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004498

Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004498

Novel molecular variants of the Na-K-2Cl cotransporter gene are responsible for antenatal Bartter syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004498

Bartter syndrome and its neonatal variant

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004498

Hypokalemia-induced downregulation of aquaporin-2 water channel expression in rat kidney medulla and cortex

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004498

Bartter's syndrome, nephrocalcinosis and renal insufficiency

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004498

Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004498

Antenatal Bartter's syndrome: why is this not a lethal condition?

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004498

Late-onset manifestation of antenatal Bartter syndrome as a result of residual function of the mutated renal Na+-K+-2Cl- co-transporter.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004498

Mutations in the human Na-K-2Cl cotransporter (NKCC2) identified in Bartter syndrome type I consistently result in nonfunctional transporters

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3004498

Phenotypic variability in Bartter syndrome type I

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21189980

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

"Neonatal variant" of Bartter syndrome presenting with acidosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21189980

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Functional Characterization of a Calcium-Sensing Receptor Mutation in Severe Autosomal Dominant Hypocalcemia with a Bartter-Like Syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21189980

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3345/KJP.2010.53.8.809

1 reference

2 August 2017

1 reference

2 August 2017

1 reference