Increased urinary prostaglandin E2 metabolite: A potential therapeutic target of Gitelman syndrome-Reference-Cited by-同舟云学术

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Increased urinary prostaglandin E2 metabolite: A potential therapeutic target of Gitelman syndrome

Published:2017-07-10 Issue:7 Volume:12 Page:e0180811
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Peng Xiaoyan,Jiang Lanping,Chen Chen,Qin Yan,Yuan Tao,Wang Ou,Xing Xiaoping,Li Xuemei,Nie Min,Chen Limeng

Funder

Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences

National Natural Science Foundation of China

Capital Specialized Clinical Application Project

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference37 articles.

1. Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference;A Blanchard;Kidney Int,2017

2. Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects;HW Seyberth;Pediatr Nephrol,2011

3. Normal Prostaglandinuria E2 in Gitelman’s Syndrome, the Hypocalciuric Variant of Bartter's Syndrome;C Luthy;Am J Kidney Dis,1995

4. A severe phenotype of Gitelman syndrome with increased prostaglandin excretion and favorable response to indomethacin;N Larkins;Clinical kidney journal,2014

5. Dose related growth response to indometacin in Gitelman syndrome;LC Liaw;Arch Dis Child,1999

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1. Genetic Foundation of Prostaglandin Metabolism Influences Patent Ductus Arteriosus Closure in Extremely Low Birth Weight Infants;American Journal of Perinatology;2024-05-31

2. A case of Gitelman syndrome with homozygous SLC12A3 deletion presenting with epilepsy;Acta Epileptologica;2023-11-29

3. Long-Term Indomethacin Treatment in a Chinese Child with Gitelman Syndrome: Case Report and Literature Review on its Efficacy and Tolerance;American Journal of Case Reports;2023-11-02

4. Frequent SLC12A3 mutations in Chinese Gitelman syndrome patients: structure and function disorder;Endocrine Connections;2022-01-01

5. Inherited Disorders of Sodium and Potassium Handling;Pediatric Nephrology;2022

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