(Q46218211)

20 December 2017

title

Chronic renal failure in a boy with classic Bartter's syndrome due to a novel mutation in CLCNKB coding for the chloride channel (English)

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20 December 2017

author name string

Chien-Ming Lin

1

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20 December 2017

Jeng-Daw Tsai

2

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20 December 2017

Yi-Fen Lo

3

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20 December 2017

Ming-Tso Yan

4

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20 December 2017

Sung-Sen Yang

5

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20 December 2017

Shih-Hua Lin

6

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20 December 2017

publication date

3 December 2008

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20 December 2017

European Journal of Pediatrics

published in

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20 December 2017

volume

168

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20 December 2017

issue

9

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20 December 2017

page(s)

1129-1133

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20 December 2017

https://scigraph.springernature.com/pub.10.1007/s00431-008-0883-y

exact match

0 references

cites work

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

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00431-008-0883-Y

Increased ammoniagenesis as a determinant of progressive renal injury

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00431-008-0883-Y

Non-steroidal anti-inflammatory drug-associated nephrotoxicity in Bartter syndrome

21 January 2018

1 reference

12 December 2020

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK

1 reference

12 December 2020

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

1 reference

12 December 2020

Prenatal and postnatal management of hyperprostaglandin E syndrome after genetic diagnosis from amniocytes.

1 reference

12 December 2020

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

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

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

1 reference

12 December 2020

Novel mutations of the chloride channel Kb gene in two Japanese patients clinically diagnosed as Bartter syndrome with hypocalciuria

1 reference

12 December 2020

Pre-pubertal growth in the hyperprostaglandin E syndrome

1 reference

12 December 2020

Renin-stimulated TGF-beta1 expression is regulated by a mitogen-activated protein kinase in mesangial cells.

1 reference

12 December 2020

Molecular analysis of the CLCNKB gene in Japanese patients with classic Bartter syndrome

1 reference

12 December 2020

Patients with biallelic mutations in the chloride channel gene CLCNKB: long-term management and outcome

1 reference

12 December 2020

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

1 reference

12 December 2020

Salt wasting and deafness resulting from mutations in two chloride channels

1 reference

12 December 2020

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

1 reference

12 December 2020

Clinical acute renal failure with nonsteroidal anti-inflammatory drugs

1 reference

12 December 2020

Hypokalemic nephropathy in the rat. Role of ammonia in chronic tubular injury

1 reference

12 December 2020

Local angiotensin II and transforming growth factor-beta1 in renal fibrosis of rats

1 reference

12 December 2020

Molecular analysis of patients with type III Bartter syndrome: picking up large heterozygous deletions with semiquantitative PCR

1 reference

12 December 2020

Association between activating mutations of calcium-sensing receptor and Bartter's syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Bartter syndrome and focal segmental glomerulosclerosis: a possible link between two diseases

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S00431-008-0883-Y

Identifiers

DOI

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20 December 2017

1 reference

20 December 2017