Genetic diagnosis and treatment of hereditary renal tubular disease with hypokalemia and alkalosis
Author:
Funder
National Natural Science Foundation of China
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
https://link.springer.com/content/pdf/10.1007/s40620-022-01428-4.pdf
Reference70 articles.
1. Downie ML, Lopez Garcia SC, Kleta R, Bockenhauer D (2021) Inherited tubulopathies of the kidney: insights from genetics. Clin J Am Soc Nephrol 16(4):620–630. https://doi.org/10.2215/CJN.14481119
2. Zelikovic I (2001) Molecular pathophysiology of tubular transport disorders. Pediatr Nephrol 16(11):919–935. https://doi.org/10.1007/s004670100671
3. Cunha TDS, Heilberg IP (2018) Bartter syndrome: causes, diagnosis, and treatment. Int J Nephrol Renovasc Dis 11:291–301. https://doi.org/10.2147/IJNRD.S155397
4. Calò L, Davis PA, Semplicini A (2002) Reduced content of alpha subunit of Gq protein content in monocytes of Bartter and Gitelman syndromes: relationship with vascular hyporeactivity. Kidney Int 61(1):353–354. https://doi.org/10.1046/j.1523-1755.2002.00128.x
5. Nunez-Gonzalez L, Carrera N, Garcia-Gonzalez MA (2021) Molecular basis, diagnostic challenges and therapeutic approaches of Bartter and Gitelman syndromes: a primer for Clinicians. Int J Mol Sci 22(21):11414. https://doi.org/10.3390/ijms222111414
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3. Tubulopathies with hypokalemic alkalosis: Bartter and HELIX syndromes in children;Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics);2023-07-14
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