(Q36705399)

15 August 2017

0 references

Gitelman or Bartter type 3 syndrome? A case of distal convoluted tubulopathy caused by CLCNKB gene mutation (English)

1 reference

15 August 2017

Alexandra Olaya Castro

series ordinal

2

object named as

Alexandra Castro

1 reference

15 August 2017

António José Cruz

1

1 reference

15 August 2017

22 January 2013

1 reference

15 August 2017

1 reference

15 August 2017

2013

1 reference

Understanding Bartter syndrome and Gitelman syndrome

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

Bartter's and Gitelman's syndromes: their relationship to the actions of loop and thiazide diuretics

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

An approach to the patient with severe hypokalaemia: the potassium quiz.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

Bartter's and Gitelman's syndromes: from gene to clinic

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

Bartter syndrome type 3: an unusual cause of nephrolithiasis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

Does hypokalaemia cause nephropathy? An observational study of renal function in patients with Bartter or Gitelman syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

The pharmacological characteristics of molecular-based inherited salt-losing tubulopathies

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

Diagnosis of hypokalemia: a problem-solving approach to clinical cases.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3604527

A thiazide test for the diagnosis of renal tubular hypokalemic disorders

5 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23345488

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/23345488

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/BCR-2012-007929

1 reference

15 August 2017

1 reference

PMC publication ID

3604527

15 August 2017

PubMed publication ID

23345488

1 reference

PMC publication ID

3604527