Publication Name	World Journal of Clinical Cases
Manuscript ID	54184
Country	China

Received	2020-01-14 05:29
Peer-Review Started	2020-01-14 05:29
To Make the First Decision
Return for Revision	2020-04-08 02:07
Revised	2020-04-25 01:46
Second Decision	2020-05-28 09:08
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief	2020-05-28 20:30
Articles in Press	2020-05-28 20:30
Publication Fee Transferred
Edit the Manuscript by Language Editor	2020-06-03 04:18
Typeset the Manuscript	2020-06-19 06:33
Publish the Manuscript Online	2020-06-24 07:33

ISSN	2307-8960 (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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Website	http://www.wjgnet.com

Category	Hematology
Manuscript Type	Case Report
Article Title	Comprehensive treatment of rare multiple endocrine neoplasia type 1: A case report
Manuscript Source	Unsolicited Manuscript
All Author List	Chen-Hui Ma, Huai-Bin Guo, Xin-Yan Pan and Wan-Xing Zhang
ORCID	Author(s) ORCID Number Chen-Hui Ma http://orcid.org/0000-0001-6254-1441 Huai-Bin Guo http://orcid.org/0000-0002-0684-5288 Xin-Yan Pan http://orcid.org/0000-0002-6998-3717 Wan-Xing Zhang http://orcid.org/0000-0001-6354-8004
Funding Agency and Grant Number
Corresponding Author	Wan-Xing Zhang, MD, Chief Doctor, Professor, Department of Hepatobiliary, Hebei General Hospital, No. 348, Heping West Road, Xinhua District, Shijiazhuang 050017, Hebei Province, China. zhangwx12@hotmail.com
Key Words	Multiple endocrine neoplasia type 1; Thymic carcinoid; Neuroendocrine tumor; Case report; Pancreas; Tumor
Core Tip	Genetic screening is recommended in patients with a family history of multiple endocrine neoplasia type 1 who present with primary hyperparathyroidism and pituitary tumors or gastrointestinal neuroendocrine tumors.
Publish Date	2020-06-24 07:33
Citation	Ma CH, Guo HB, Pan XY, Zhang WX. Comprehensive treatment of rare multiple endocrine neoplasia type 1: A case report. World J Clin Cases 2020; 8(12): 2647-2654
URL	https://www.wjgnet.com/2307-8960/full/v8/i12/2647.htm
DOI	https://dx.doi.org/10.12998/wjcc.v8.i12.2647

Full Article (PDF)	WJCC-8-2647.pdf
Full Article (Word)	WJCC-8-2647.docx
Manuscript File	54184-Review-Filipodia.docx
Answering Reviewers	54184-Answering reviewers.pdf
Audio Core Tip	54184-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	54184-Conflict-of-interest statement.pdf
Copyright License Agreement	54184-Copyright license agreement.pdf
Signed Informed Consent Form(s) or Document(s)	54184-Informed consent statement.pdf
Non-Native Speakers of English Editing Certificate	54184-Language certificate.pdf
Peer-review Report	54184-Peer-review(s).pdf
Scientific Misconduct Check	54184-Bing-Zhang L-1.png
Scientific Misconduct Check	54184-Bing-Dou Y-2.png
Scientific Misconduct Check	54184-Scientific misconduct check.pdf
Scientific Editor Work List	54184-Scientific editor work list.pdf