(Q28304558)

17

Rosa Vargas-Poussou

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Marie-Alice Macher

6

Marie-Alice Macher

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Xavier Jeunemaitre

16

Xavier Jeunemaître

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Georges Deschênes

7

Georges Deschenes

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5

Patrick Niaudet

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author name string

Karine Brochard

1

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Olivia Boyer

2

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Anne Blanchard

3

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Marie-Alice Macher

6

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Georges Deschenes

7

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Albert Bensman

8

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Stéphane Decramer

9

0 references

Pierre Cochat

10

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Denis Morin

11

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Françoise Broux

12

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Mathilde Caillez

13

0 references

Claude Guyot

14

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Robert Novo

15

0 references

Xavier Jeunemaître

16

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Rosa Vargas-Poussou

Nephrology Dialysis Transplantation

17

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language of work or name

English

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publication date

May 2009

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published in

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volume

24

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issue

5

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page(s)

1455-64

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cites work

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

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Genetic disorders of renal electrolyte transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Role of prostaglandins in hyperprostaglandin E syndrome and in selected renal tubular disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Bartter syndrome and its neonatal variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Hypokalemic salt-losing tubulopathy with chronic renal failure and sensorineural deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Antenatal Bartter syndrome with sensorineural deafness: refinement of the locus on chromosome 1p31.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

A simple estimate of glomerular filtration rate in full-term infants during the first year of life

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Urinary phosphate/creatinine, calcium/creatinine, and magnesium/creatinine ratios in a healthy pediatric population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Mouse model of type II Bartter's syndrome. I. Upregulation of thiazide-sensitive Na-Cl cotransport activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Mouse model of type II Bartter's syndrome. II. Altered expression of renal sodium- and water-transporting proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Localization and functional characterization of rat kidney-specific chloride channel, ClC-K1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

The neonatal variant of Bartter syndrome and deafness: preservation of renal function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Evaluation of long-term treatment with indomethacin in hereditary hypokalemic salt-losing tubulopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Aldosterone as a mediator of progressive renal disease: pathogenetic and clinical implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

The role of renin-angiotensin-aldosterone system in the progression of chronic kidney disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Long-term renal follow-up of extremely low birth weight infants

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Low birth weight increases risk for end-stage renal disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Functional heterogeneity of ROMK mutations linked to hyperprostaglandin E syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Classification and rescue of ROMK mutations underlying hyperprostaglandin E syndrome/antenatal Bartter syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689

Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNDT%2FGFN689