(Q24311551)

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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

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8528245%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

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

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8528245%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

David H. Ellison

4

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Europe PubMed Central

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14 October 2019

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14 October 2019

Francisco Javier Gainza

11

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Europe PubMed Central

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14 October 2019

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Simon DB

1

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14 October 2019

Nelson-Williams C

2

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Europe PubMed Central

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14 October 2019

Bia MJ

3

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14 October 2019

Molina AM

6

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Europe PubMed Central

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14 October 2019

Vaara I

7

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Europe PubMed Central

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14 October 2019

Iwata F

8

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Europe PubMed Central

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14 October 2019

Cushner HM

9

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14 October 2019

Koolen M

10

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14 October 2019

Gitleman HJ

12

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14 October 2019

Lifton RP

13

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Europe PubMed Central

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14 October 2019

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1 January 1996

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Europe PubMed Central

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14 October 2019

Nature Genetics

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14 October 2019

12

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14 October 2019

1

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14 October 2019

24-30

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8528245%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

Pathogenesis of Bartter's syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

21 January 2018

The physiologic basis of diuretic synergism: its role in treating diuretic resistance

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

21 January 2018

Renal Magnesium Wasting in Bartter's Syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

21 January 2018

Genetic determinants of human hypertension

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Prostaglandins and Bartter's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Bartter's syndrome and the atrial natriuretic factor gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Inheritance of Bartter syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Resistance to endogenous norepinephrine in Bartter's syndrome: reversion during indomethacin administration.

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Chronic hypomagnesemia and hypokalemia due to renal wasting in siblings.

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial hypokalemia-hypomagnesemia or Gitelman's syndrome: a further case

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Growth Characteristics in Patients with Bartter’s Syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Low urinary calcium excretion in Bartter's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Bartter's syndrome: the unsolved puzzle

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Angiotensin II type 1 receptor gene abnormality in a patient with Bartter's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Primary structure and functional expression of a cDNA encoding the thiazide-sensitive, electroneutral sodium-chloride cotransporter

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

The 1993-94 Généthon human genetic linkage map

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

A PCR-Based Genetic Linkage Map of Human Chromosome 16

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Does magnesium play a role in the hypokalemia of Bartter's syndrome?

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Vasoactive peptides in Bartter's syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

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inferred from DOI database lookup

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0196-24

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/NG0196-24

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8528245%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

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0 references

release_lcwhq2rxnfbc3p2gz56bvkovkq

1 reference

https://api.fatcat.wiki/v0/release/lcwhq2rxnfbc3p2gz56bvkovkq

24 November 2022

based on heuristic

mapped directly with Wikidata item

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8528245%20AND%20SRC:MED&resulttype=core&format=json

14 October 2019

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