(Q37774787)

23 August 2017

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title

Gitelman syndrome: pathophysiological and clinical aspects (English)

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23 August 2017

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G Graziani

1

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23 August 2017

C Fedeli

2

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23 August 2017

L Moroni

3

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23 August 2017

L Cosmai

4

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23 August 2017

S Badalamenti

5

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23 August 2017

C Ponticelli

6

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23 August 2017

language of work or name

English

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publication date

22 July 2010

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QJM: An International Journal of Medicine

23 August 2017

published in

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23 August 2017

volume

103

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23 August 2017

issue

10

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23 August 2017

page(s)

741-748

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Genetic disorders of renal electrolyte transport

23 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

Novel thiazide-sensitive Na-Cl cotransporter mutation in a Chinese patient with Gitelman's syndrome presenting as hypokalaemic paralysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

Expression and localisation of the pyrophosphate transporter, ANK, in murine kidney cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

Inherited forms of renal hypomagnesemia: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

TRPM6 forms the Mg2+ influx channel involved in intestinal and renal Mg2+ absorption

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

Thiazide-induced hypocalciuria is accompanied by a decreased expression of Ca2+ transport proteins in kidney

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

A trail of research on potassium

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

Inherited primary renal tubular hypokalemic alkalosis: a review of Gitelman and Bartter syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

Electrocardiogram with prolonged QT interval in Gitelman disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

Cardiac work up in primary renal hypokalaemia-hypomagnesaemia (Gitelman syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCQ123

21 January 2018

Identifiers

DOI

10.1093/QJMED/HCQ123

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23 August 2017

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