Gitelman Syndrome
What's New
Last Posted: Nov 07, 2019
- High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults.
Hureaux Marguerite et al. Kidney international 2019 Sep - The challenges of diagnosis and management of Gitelman syndrome.
Urwin Stephanie et al. Clinical endocrinology 2019 Oct - Clinical and Genetic Characteristics in Patients With Gitelman Syndrome.
Fujimura Junya et al. Kidney international reports 2019 Jan 4(1) 119-125 - Hydrochlorothiazide Test as a Tool in the Diagnosis of Gitelman Syndrome in Chinese Patients.
Peng Xiaoyan et al. Frontiers in endocrinology 2018 9559 - Genetic screening for Bartter syndrome and Gitelman syndrome pathogenic genes among individuals with hypertension and hypokalemia.
Bao Minghui et al. Clinical and experimental hypertension (New York, N.Y. : 1993) 2018 Jun 1-8 - Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.
Ashton Emma J et al. Kidney international 2018 Feb
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- Page last reviewed:Oct 1, 2020
- Page last updated:Dec 29, 2020
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