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Journal Abstract Search
238 related items for PubMed ID: 28819721
1. Inherited, not acquired, Gitelman syndrome in a patient with Sjögren's syndrome: importance of genetic testing to distinguish the two forms. Mishima E, Mori T, Sohara E, Uchida S, Abe T, Ito S. CEN Case Rep; 2017 Nov; 6(2):180-184. PubMed ID: 28819721 [Abstract] [Full Text] [Related]
6. Acquired gitelman syndrome. Kim YK, Song HC, Kim YS, Choi EJ. Electrolyte Blood Press; 2009 Jun; 7(1):5-8. PubMed ID: 21468178 [Abstract] [Full Text] [Related]
7. A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome with diabetes and the choices of the appropriate hypoglycemic drugs: a case report. Liu Z, Wang S, Zhang R, Wang C, Lu J, Shao L. BMC Med Genomics; 2021 Aug 04; 14(1):198. PubMed ID: 34348722 [Abstract] [Full Text] [Related]
11. Novel SLC12A3 gene mutations and clinical characteristics in two pedigrees with Gitelman syndrome. Ying Q, Ye Z, Zhang W, Pan Y, Dai L, Lin K, Feng X, Dong X, He F. Clin Endocrinol (Oxf); 2023 Nov 04; 99(5):474-480. PubMed ID: 36562655 [Abstract] [Full Text] [Related]
12. Renal calcium and magnesium handling in Gitelman syndrome. Reyes JV, Medina PMB. Am J Transl Res; 2022 Nov 04; 14(1):1-19. PubMed ID: 35173827 [Abstract] [Full Text] [Related]
13. A novel homozygous SLC12A3 mutation causing Gitelman syndrome with co-existent autoimmune thyroiditis: a case report and review of the literature. Koca O, Alay MT, Murt A, Kalayci Yigin A, Seven M, Bavunoglu I. CEN Case Rep; 2024 Oct 04; 13(5):330-338. PubMed ID: 38308744 [Abstract] [Full Text] [Related]
19. Gitelman syndrome as a cause of psychomotor retardation in a toddler. Skalova S, Neuman D, Lnenicka P, Stekrova J. Arab J Nephrol Transplant; 2013 Jan 04; 6(1):37-9. PubMed ID: 23282232 [Abstract] [Full Text] [Related]