(Q79295165)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17061123%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

0 references

1 reference

title

Gitelman's syndrome: towards genotype-phenotype correlations? (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17061123%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

1 reference

Eva Riveira-Munoz

1

1 reference

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21 December 2019

Qing Chang

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17061123%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

René J Bindels

series ordinal

3

1 reference

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21 December 2019

Olivier Devuyst

series ordinal

4

1 reference

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21 December 2019

publication date

24 October 2006

1 reference

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21 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17061123%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

volume

22

1 reference

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21 December 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17061123%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

page(s)

326-332

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17061123%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00467-006-0321-1

21 December 2019

exact match

0 references

cites work

Enhanced passive Ca2+ reabsorption and reduced Mg2+ channel abundance explains thiazide-induced hypocalciuria and hypomagnesemia

1 reference

12 December 2020

Altered renal distal tubule structure and renal Na(+) and Ca(2+) handling in a mouse model for Gitelman's syndrome.

1 reference

12 December 2020

A serum potassium level above 10 mmol/l in a patient predisposed to hypokalemia

1 reference

12 December 2020

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

1 reference

12 December 2020

Hypokalemia in a mouse model of Gitelman's syndrome

1 reference

12 December 2020

Gitelman's not-so-benign syndrome

1 reference

12 December 2020

Novel NCCT gene mutations as a cause of Gitelman's syndrome and a systematic review of mutant and polymorphic NCCT alleles.

1 reference

12 December 2020

Molecular physiology of cation-coupled Cl? cotransport: the SLC12 family

1 reference

12 December 2020

Clinical presentation of genetically defined patients with hypokalemic salt-losing tubulopathies.

1 reference

12 December 2020

Intrafamilial phenotype variability in patients with Gitelman syndrome having the same mutations in their thiazide-sensitive sodium/chloride cotransporter

1 reference

12 December 2020

Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome

1 reference

12 December 2020

Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes

1 reference

12 December 2020

Primary structure and functional expression of a cDNA encoding the thiazide-sensitive, electroneutral sodium-chloride cotransporter

1 reference

12 December 2020

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

1 reference

12 December 2020

Pathophysiology of functional mutations of the thiazide-sensitive Na-Cl cotransporter in Gitelman disease

1 reference

12 December 2020

Phenotype resembling Gitelman's syndrome in mice lacking the apical Na+-Cl- cotransporter of the distal convoluted tubule

1 reference

12 December 2020

Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype

1 reference

12 December 2020

Functional expression of the human thiazide-sensitive NaCl cotransporter in Madin-Darby canine kidney cells.

1 reference

12 December 2020

A new mutation (intron 9 +1 G>T) in the SLC12A3 gene is linked to Gitelman syndrome in Gypsies

1 reference

12 December 2020

Estradiol enhances thiazide-sensitive NaCl cotransporter density in the apical plasma membrane of the distal convoluted tubule in ovariectomized rats

1 reference

12 December 2020

Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain

1 reference

12 December 2020

N-Glycosylation at two sites critically alters thiazide binding and activity of the rat thiazide-sensitive Na(+):Cl(-) cotransporter.

1 reference

12 December 2020

Functional expression of mutations in the human NaCl cotransporter: evidence for impaired routing mechanisms in Gitelman's syndrome

1 reference

12 December 2020

Salt wasting and deafness resulting from mutations in two chloride channels

1 reference

12 December 2020

Pharmacotyping of hypokalaemic salt-losing tubular disorders

1 reference

12 December 2020

Gitelman's syndrome revisited: an evaluation of symptoms and health-related quality of life.

1 reference

12 December 2020

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

1 reference

12 December 2020

A new familial disorder characterized by hypokalemia and hypomagnesemia

1 reference

12 December 2020