Publication Name	World Journal of Nephrology
Manuscript ID	12744
Country	United States

Received	2014-07-24 08:25
Peer-Review Started	2014-07-24 15:23
To Make the First Decision	2014-08-14 14:56
Return for Revision	2014-08-17 12:01
Revised	2014-08-29 01:40
Second Decision	2015-01-28 11:58
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2015-02-09 09:29
Articles in Press	2015-02-09 09:29
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2015-04-09 17:48
Publish the Manuscript Online	2015-05-08 14:17

ISSN	2220-6124 (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	Urology & Nephrology
Manuscript Type	Minireviews
Article Title	Primary and secondary hyperoxaluria: Understanding the enigma
Manuscript Source	Invited Manuscript
All Author List	Bhavna Bhasin, Hatice Melda Ürekli and Mohamed G Atta
Funding Agency and Grant Number
Corresponding Author	Dr. Mohamed Atta, MD, Division of Nephrology, Johns Hopkins University,1830 E. Monument Street, Suite 416, Baltimore, MD 21287, United States. matta1@jhmi.edu
Key Words	Primary hyperoxaluria; Secondary hyperoxaluria; Renal stones; Renal failure; Transplantation
Core Tip	Hyperoxaluria is a disorder characterized by increased urinary oxalate excretion. Primary hyperoxaluria is an inherited defect of oxalate metabolism while secondary hypeoxaluria is seen in states of increased ingestion of oxalate, its percursors or altered gut flora. These disorders can lead to recurrent renal stones, nephrocalcinosis and eventually end stage renal disease. Despite these common features, the sub types of hyperoxaluria differ in their pathogenesis, severity of clinical presentation and treatment plan. Prompt clinical recognition and distinction between these disorders is essential not only for timely intervention but also impacts prognosis in patients with hyperoxaluria.
Publish Date	2015-05-08 14:17
Citation	Bhasin B, Ürekli HM, Atta MG. Primary and secondary hyperoxaluria: Understanding the enigma. World J Nephrol 2015; 4(2): 235-244
URL	http://www.wjgnet.com/2220-6124/full/v4/i2/235.htm
DOI	http://dx.doi.org/10.5527/wjn.v4.i2.235

Full Article (PDF)	WJN-4-235.pdf
Full Article (Word)	WJN-4-235.doc
Manuscript File	12744-Review.docx
Answering Reviewers	12744-Answering reviewers.pdf
Conflict-of-Interest Disclosure Form	12744-Conflict-of-interest statement.pdf
Copyright License Agreement	12744-Copyright assignment.pdf
Peer-review Report	12744-Peer-review(s).pdf
Scientific Misconduct Check	12744-Scientific misconduct check.pdf
Scientific Editor Work List	12744-Scientific editor work list.pdf