(Q52044722)

20 April 2018

title

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

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20 April 2018

main subject

patient

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author

Hannsjörg W. Seyberth

8

object named as

Hannsjörg W Seyberth

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20 April 2018

author name string

Melanie Peters

1

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20 April 2018

Nikola Jeck

2

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20 April 2018

Stephan Reinalter

3

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20 April 2018

Andreas Leonhardt

4

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20 April 2018

Burkhard Tönshoff

5

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20 April 2018

G ünter Klaus G

6

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20 April 2018

Martin Konrad

7

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20 April 2018

language of work or name

English

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publication date

1 February 2002

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20 April 2018

American Journal of Medicine

published in

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20 April 2018

volume

112

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20 April 2018

issue

3

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20 April 2018

page(s)

183-190

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20 April 2018

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

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Impaired response to furosemide in hyperprostaglandin E syndrome: evidence for a tubular defect in the loop of Henle

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Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes [published e

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Cloning, tissue distribution, and intrarenal localization of ClC chloride channels in human kidney

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

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

7 January 2021

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A hyperprostaglandin E syndrome mutation in Kir1.1 (renal outer medullary potassium) channels reveals a crucial residue for channel function in Kir1.3 channels

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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10.1016/S0002-9343(01)01086-5

7 January 2021

Identifiers

DOI

1 reference

20 April 2018

PubMed ID

11893344

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20 April 2018