Publication Name	World Journal of Gastroenterology
Manuscript ID	82847
Country	Türkiye

Received	2022-12-28 11:27
Peer-Review Started	2022-12-28 11:28
To Make the First Decision
Return for Revision	2023-02-01 21:39
Revised	2023-02-15 10:10
Second Decision	2023-04-28 03:33
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2023-05-01 16:02
Articles in Press	2023-05-01 16:02
Publication Fee Transferred
Edit the Manuscript by Language Editor	2023-05-31 10:59
Typeset the Manuscript	2023-06-16 01:38
Publish the Manuscript Online	2023-06-28 07:41

ISSN	1007-9327 (print) and 2219-2840 (online)
Open Access	This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (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	Gastroenterology & Hepatology
Manuscript Type	Review
Article Title	Glycogen storage diseases: An update
Manuscript Source	Invited Manuscript
All Author List	Ersin Gümüş and Hasan Özen
ORCID	Author(s) ORCID Number Ersin Gümüş http://orcid.org/0000-0002-2280-9789 Hasan Özen http://orcid.org/0000-0002-9063-3893
Funding Agency and Grant Number
Corresponding Author	Hasan Özen, MD, Professor, Department of Pediatric Gastroenterology, Hepatology and Nutrition, Hacettepe University Faculty of Medicine, Ihsan Dogramaci Children’s Hospital, Gevher Nesibe Cad., Ankara 06230, Türkiye. haozen@hacettepe.edu.tr
Key Words	Glycogen storage disease; Liver; Muscle; Hypoglycemia
Core Tip	Glycogen storage diseases are multisystemic diseases that can present at any age. Primarily affected organs are liver and skeletal muscle, but heart, central nervous system, kidneys, intestines, and other organs may also be affected. Since the initial presenting symptoms can occur in adulthood, it is a group of rare diseases that should be recognized and managed by not only pediatricians but also physicians taking care of adults.
Publish Date	2023-06-28 07:41
Citation	Gümüş E, Özen H. Glycogen storage diseases: An update. World J Gastroenterol 2023; 29(25): 3932-3963
URL	https://www.wjgnet.com/1007-9327/full/v29/i25/3932.htm
DOI	https://dx.doi.org/10.3748/wjg.v29.i25.3932

Full Article (PDF)	WJG-29-3932-with-cover.pdf
Full Article (Word)	WJG-29-3932.docx
Manuscript File	82847_Auto_Edited-LM-Language editing-Webster J-Clear.docx
Answering Reviewers	82847-Answering reviewers.pdf
Audio Core Tip	82847-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	82847-Conflict-of-interest statement.pdf
Copyright License Agreement	82847-Copyright license agreement.pdf
Non-Native Speakers of English Editing Certificate	82847-Language certificate.pdf
Peer-review Report	82847-Peer-review(s).pdf
Scientific Misconduct Check	82847-Bing-Wang JJ-2.png
Scientific Editor Work List	82847-Scientific editor work list.pdf