(Q81303717)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17873326%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

title

Two novel genotypes of the thiazide-sensitive Na-Cl cotransporter (SLC12A3) gene in patients with Gitelman's syndrome (English)

1 reference

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7 January 2020

author name string

Noriko Aoi

1

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7 January 2020

Tomohiro Nakayama

2

1 reference

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7 January 2020

Yoshiko Tahira

3

1 reference

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7 January 2020

Akira Haketa

4

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7 January 2020

Minako Yabuki

5

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7 January 2020

Tadataka Sekiyama

6

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7 January 2020

Chie Nakane

7

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7 January 2020

Hiroaki Mano

8

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7 January 2020

Hideomi Kawachi

9

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7 January 2020

Naoyuki Sato

10

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7 January 2020

Masayoshi Soma

11

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7 January 2020

Kouichi Matsumoto

12

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7 January 2020

publication date

1 April 2007

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7 January 2020

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7 January 2020

volume

31

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7 January 2020

issue

2

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7 January 2020

page(s)

149-153

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https://scigraph.springernature.com/pub.10.1007/s12020-007-0024-9

7 January 2020

exact match

0 references

cites work

Concomitant occurrence of Gitelman and Bartter syndromes in the same family?

1 reference

12 December 2020

Enhanced passive Ca2+ reabsorption and reduced Mg2+ channel abundance explains thiazide-induced hypocalciuria and hypomagnesemia

1 reference

12 December 2020

The molecular basis of hypokalaemic alkalosis: Bartter's and Gitelman's syndromes

1 reference

12 December 2020

The association of periodic paralysis and hyperthyroidism in Japan

1 reference

12 December 2020

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

1 reference

12 December 2020

Effects of thyroid status on renal calcium and magnesium handling.

1 reference

12 December 2020

Magnesium metabolism in hyperthyroidism and hypothyroidism

1 reference

12 December 2020

Effects of Electrolyte Disorders on Renal Structure and Function

1 reference

12 December 2020

Defective processing and expression of thiazide-sensitive Na-Cl cotransporter as a cause of Gitelman's syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Novel mutations in thiazide-sensitive Na-Cl cotransporter gene of patients with Gitelman's syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Functional confirmation of Gitelman's syndrome mutations in Japanese.

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

1 reference

12 December 2020

A novel mutation in Ca2+-sensing receptor gene in familial hypocalciuric hypercalcemia

1 reference

12 December 2020

Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)

1 reference

12 December 2020

Periodic paralysis complicating thyrotoxicosis in Chinese

1 reference

12 December 2020

Analysis of renal tubular electrolyte transporter genes in seven patients with hypokalemic metabolic alkalosis

1 reference

12 December 2020

Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain

1 reference

12 December 2020

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

1 reference

12 December 2020

A high prevalence of Gitelman's syndrome mutations in Japanese

1 reference

12 December 2020

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

1 reference

12 December 2020

Isolation of the 5'-flanking region of genes by thermal asymmetric interlaced polymerase chain reaction

1 reference

12 December 2020

Exchangeable potassium and sodium in hyperthyroidism and hypothyroidism

1 reference

12 December 2020

Chronic renal failure, end-stage renal disease, and peritoneal dialysis in Gitelman's syndrome

1 reference

12 December 2020

Four novel mutations in the thiazide-sensitive Na-Cl co-transporter gene in Japanese patients with Gitelman's syndrome

1 reference

12 December 2020

Phenotype and genotype analysis in Chinese patients with Gitelman's syndrome

1 reference

12 December 2020

A new familial disorder characterized by hypokalemia and hypomagnesemia

1 reference

12 December 2020

10.1007/S12020-007-0024-9

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17873326%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference