A serum potassium level above 10 mmol/l in a patient predisposed to hypokalemia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,General Medicine
Link
http://www.nature.com/articles/ncpneph0201.pdf
Reference18 articles.
1. Simon DB et al. (1996) Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter. Nat Genet 12: 24–30
2. Lemmink HH et al. (1998) Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain. Kidney Int 54: 720–730
3. De Jong JC et al. (2002) Functional expression of mutations in the human NaCl cotransporter: evidence for impaired routing mechanisms in Gitelman's syndrome. J Am Soc Nephrol 13: 1442–1448
4. Bartter FC et al. (1962) Hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis: a new syndrome. Am J Med 33: 811–828
5. Gitelman HJ et al. (1966) A new familial disorder characterized by hypokalemia and hypomagnesemia. Trans Assoc Am Physicians 79: 221–235
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