Search
Now showing items 11-13 of 13
Gitelman's syndrome associated with chondrocalcinosis: a case report
(INFORMA HEALTHCARE, 2013)
Gitelman's syndrome (GS) is a rare disease with autosomal recessive trait, characterized by hypokalemia, hypomagnesemia, metabolic alkalosis, hypocalciuria and hyperkinemic hyperaldosteronism. While muscle weakness, tetany, ...
Association of vitamin D receptor gene Taql, Fokl and Apal variants with arteriovenous fistula failure in hemodialysis patients
(SAGE PUBLICATIONS LTD, 2018)
Purpose: We investigated the influence of the vitamin D receptor gene Taql (rs731236), Apal (rs7975232), and Fokl (rs2228570) polymorphisms in arteriovenous fistula failure in hemodialysis patients. Methods: This study was ...