Hypocalciuria in Patients With Gitelman Syndrome: Role of Blood Volume

Author:

Cheng Chih-Jen,Shiang Jen-Chuan,Hsu Yu-Juei,Yang Sung-Sen,Lin Shih-Hua

Publisher

Elsevier BV

Subject

Nephrology

Reference32 articles.

1. A new familial disorder characterized by hypokalemia and hypomagnesemia;Gitelman;Trans Assoc Am Physicians,1966

2. Gitelman’s variant of Bartter’s syndrome, inherited hypokalemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter;Simon;Nat Genet,1996

3. Novel molecular variants of the Na-Cl cotransporter gene are responsible for Gitelman syndrome;Mastroianni;Am J Hum Genet,1996

4. Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain;Lemmink;Kidney Int,1998

5. Novel thiazide-sensitive Na-Cl cotransporter mutation in a Chinese patient with Gitelman’s syndrome presenting as hypokalaemic paralysis;Cheng;Nephrol Dial Transplant,2003

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