(Q50633126)

English

Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis.

scientific article published on 2 October 2008

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis. (English)

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

focal segmental glomerulosclerosis

1 reference

based on heuristic

inferred from title

author name string

Hajime Yamazaki

1

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

Kandai Nozu

2

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

Ichiei Narita

3

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

Michio Nagata

4

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

Yoshimi Nozu

5

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

Xue Jun Fu

6

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

Masafumi Matsuo

7

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

Kazumoto Iijima

8

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

Fumitake Gejyo

9

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

publication date

2 October 2008

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

Pediatric Nephrology

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

24

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

2

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

415-418

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

https://scigraph.springernature.com/pub.10.1007/s00467-008-0999-3

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Late-onset manifestation of antenatal Bartter syndrome as a result of residual function of the mutated renal Na+-K+-2Cl- co-transporter.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic variability in Bartter syndrome type I

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C1q nephropathy in association with Gitelman syndrome: a case report

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reversal of Bartter's syndrome by renal transplantation in a child with focal, segmental glomerular sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Podocyte injury in focal segmental glomerulosclerosis: Lessons from animal models (a play in five acts).

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progression and potential regression of glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of Gitelman's syndrome and focal glomerulosclerosis.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simultaneous Mutations in the CLCNKB and SLC12A3 Genes in Two Siblings with Phenotypic Heterogeneity in Classic Bartter Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18830715

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00467-008-0999-3

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

1 reference

Europe PubMed Central

17 March 2018

http://europepmc.org/abstract/MED/18830715

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50633126&oldid=1428645374"