A case of type III Bartterʼs syndrome with acute kidney injury
Author:
Affiliation:
1. Department of Pediatrics, Japan Community Health care Organization Chukyo Hospital
Publisher
Japanese Society for Pediatric Nephrology
Subject
Literature and Literary Theory,History,Cultural Studies
Link
https://www.jstage.jst.go.jp/article/jjpn/34/1/34_cr.2020.0186/_pdf
Reference16 articles.
1. 2) Uemura O, Nagai T, Ishikura K, Ito S, Hataya H, Gotoh Y, Fujita N, Akioka Y, Kaneko T, Honda M: Creatinine-based equation to estimate the glomerular filtration rate in Japanese children and adolescents with chronic kidney disease. Clin Exp Nephrol 2014; 18: 626-633.
2. 3) Uemura O, Ishikura K, Gotoh Y, Honda M: Creatinine-based estimated glomerular filtration rate for children younger than 2 years. Clin Exp Nephrol 2018; 22: 483-484.
3. 4) Fukuyama S, Hiramatsu M, Akagi M, Higa M, Ohta T: Novel mutations of the chloride channel Kb gene in two Japanese patients clinically diagnosed as Bartter syndrome with hypocalciuria. J Clin Endocrinol Metab 2004; 89: 5847-5850.
4. 5) Seyberth HW: An improved terminology and classification of Bartter-like syndromes. Nat Clin Pract Nephrol 2008; 4: 560-567.
5. 6) Seys E, Andrini O, Keck M, Mansour-Hendili L, Courand PY, Simian C, Deschenes G, Kwon T, Bertholet-Thomas A, Bobrie G, Borde JS, Bourdat-Michel G, Decramer S, Cailliez M, Krug P, Cozette P, Delbet JD, Dubourg L, Chaveau D, Fila M, Jourde- Chiche N, Knebelmann B, Lavocat MP, Lemoine S, Djeddi D, Llanas B, Louillet F, Merieau E, Mileva M, Mota-Vieira L, Mousson C, Nobili F, Novo R, Roussey-Kesler G, Vrillon I, Walsh SB, Teulon J, Blanchard A, Vargas-Poussou R: Clinical and genetic spectrum of Bartter syndrome Type 3. J Am Soc Nephrol 2017; 28: 2540-2552.
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