共 100 条
- [11] Mukhtar M(2016)Genotype/phenotype analysis in 67 Chinese patients with Gitelman's syndrome Am J Nephrol 44 159-584
- [12] Ahmed A(2016)Genetic features of Chinese patients with Gitelman syndrome: sixteen novel SLC12A3 mutations identified in a new cohort Am J Nephrol 44 113-17
- [13] Ullah W(2017)Genetic causes of hypomagnesemia, a clinical overview Pediatr Nephrol 32 1123-195
- [14] Saeed R(2002)Electrocardiogram with prolonged QT interval in Gitelman disease Kidney Int 62 580-1082
- [15] Hamid M(1976)Hypokalemia: causes, consequences and correction Am J Med Sci 272 5-475
- [16] Makino S(2022)Hypocalcemia-induced QT interval prolongation Cardiology 147 191-634
- [17] Tajima T(2006)Hypokalemic paralysis due to Gitelman syndrome: a family study Neurology 67 1080-undefined
- [18] Shinozuka J(2017)Increased urinary prostaglandin E2 metabolite: a potential therapeutic target of Gitelman syndrome PLoS One 12 e0180811-undefined
- [19] Ikumi A(2015)Indomethacin, amiloride, or eplerenone for treating hypokalemia in Gitelman syndrome J Am Soc Nephrol 26 468-undefined
- [20] Awaguni H(2013)The adverse effects profile of levetiracetam in epilepsy: a more detailed look Int J Neurosci 124 627-undefined