Hypocalciuria in Patients With Gitelman Syndrome: Role of Blood Volume
Author:
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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1. A Case of Gitelman Syndrome with Hypercalcemia Secondary to Primary Hyperparathyroidism;Case Reports in Endocrinology;2022-06-25
2. Gitelman syndrome with normocalciuria – a case report;BMC Nephrology;2022-05-04
3. Molecular aspects of the altered Angiotensin II signaling in Gitelman’s syndrome;Expert Opinion on Orphan Drugs;2022-05-03
4. Amiloride and calciuria;Nephrology Dialysis Transplantation;2021-07-15
5. The challenges of diagnosis and management of Gitelman syndrome;Clinical Endocrinology;2019-10-06
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