Publication Name	World Journal of Methodology
Manuscript ID	15935
Country	United Arab Emirates

Received	2014-12-18 10:14
Peer-Review Started	2014-12-18 17:54
To Make the First Decision	2015-04-27 15:33
Return for Revision	2015-04-29 20:44
Revised	2015-05-14 01:04
Second Decision	2015-05-29 15:23
Accepted by Journal Editor-in-Chief	2015-05-29 16:23
Accepted by Executive Editor-in-Chief	2015-06-08 15:59
Articles in Press	2015-06-08 16:28
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2015-06-11 19:11
Publish the Manuscript Online	2015-07-07 20:52

ISSN	2222-0682 (online)
Open Access	This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
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Category	Pediatrics
Manuscript Type	Editorial
Article Title	Bartter and Gitelman syndromes: Spectrum of clinical manifestations caused by different mutations
Manuscript Source	Invited Manuscript
All Author List	Amar Al Shibli and Hassib Narchi
Funding Agency and Grant Number
Corresponding Author	Hassib Narchi, MD, FRCPCH, Department of Pediatrics, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, PO Box 17666, United Arab Emirates. hassib.narchi@uaeu.ac.ae
Key Words	Gitelman syndrome; Bartter syndrome; Potassium; Chloride; Magnesium; Metabolic alkalosis; Genetics
Core Tip	As inherited disorders of renal tubular excretion and reabsorption of electrolytes, Bartter and Gitelman syndromes were previously considered as genotypic and phenotypic heterogeneous diseases. Although they share some characteristic features, the clinical and laboratory manifestations may not always allow distinction between them. Different genetic mutations inducing impairment of electrolytes transport across different sites of the nephron have been reported in each condition. However, considerable overlap exists between the different genotypes and phenotypes of these two conditions that are now better described as a spectrum of clinical manifestations caused by different gene mutations.
Publish Date	2015-07-07 20:52
Citation	Al Shibli A, Narchi H. Bartter and Gitelman syndromes: Spectrum of clinical manifestations caused by different mutations. World J Methodol 2015; 5(2): 55-61
URL	http://www.wjgnet.com/2222-0682/full/v5/i2/55.htm
DOI	http://dx.doi.org/10.5662/wjm.v5.i2.55

Full Article (PDF)	WJM-5-55.pdf
Full Article (Word)	WJM-5-55.doc
Manuscript File	15935-Review.docx
Answering Reviewers	15935-Answering reviewers.pdf
Audio Core Tip	15935-Audio core tip.mp3
Conflict-of-Interest Disclosure Form	15935-Conflict-of-interest statement.pdf
Copyright License Agreement	15935-Copyright assignment.pdf
Peer-review Report	15935-Peer-review(s).pdf
Journal Editor-in-Chief Review Report	15935-Journal editor-in-chief review report.pdf
Scientific Misconduct Check	15935-Scientific misconduct check.pdf
Scientific Editor Work List	15935-Scientific editor work list.pdf