Publication Name	World Journal of Hepatology
Manuscript ID	83748
Country	Italy

Received	2023-02-07 19:46
Peer-Review Started	2023-02-07 19:49
To Make the First Decision
Return for Revision	2023-03-22 18:08
Revised	2023-04-04 21:46
Second Decision	2023-04-11 02:59
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2023-04-12 03:44
Articles in Press	2023-04-12 03:44
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript	2023-05-17 05:48
Publish the Manuscript Online	2023-05-24 09:31

ISSN	1948-5182 (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	Minireviews
Article Title	Current guidelines for diagnosis and management of hepatic involvement in hereditary hemorrhagic teleangiectasia
Manuscript Source	Invited Manuscript
All Author List	Luca Ielasi, Matteo Tonnini, Fabio Piscaglia and Ilaria Serio
ORCID	Author(s) ORCID Number Luca Ielasi http://orcid.org/0000-0003-4162-2319 Fabio Piscaglia http://orcid.org/0000-0001-8264-1845 Ilaria Serio http://orcid.org/0000-0002-6676-4148
Funding Agency and Grant Number
Corresponding Author	Luca Ielasi, MD, Doctor, Department of Medical and Surgical Sciences, University of Bologna, Via Albertoni, 15, Bologna 40138, Italy. luca.ielasi.kr@gmail.com
Key Words	Hereditary hemorrhagic teleangiectasia; Rendu-Osler-Weber syndrome; Hepatic vascular malformations; Liver
Core Tip	Hereditary hemorrhagic teleangiectasia (HHT) is the most common cause of hepatic vascular malformation in adults. Although liver involvement is common in HHT, most patients do not present any hepatic-related symptoms. Unfortunately, some patients have severe forms of disease with refractory medical conditions related to the hepatic vascular malformations. For those patients the only definitive treatment available at present is liver transplantation.
Publish Date	2023-05-24 09:31
Citation	Ielasi L, Tonnini M, Piscaglia F, Serio I. Current guidelines for diagnosis and management of hepatic involvement in hereditary hemorrhagic teleangiectasia. World J Hepatol 2023; 15(5): 675-687
URL	https://www.wjgnet.com/1948-5182/full/v15/i5/675.htm
DOI	https://dx.doi.org/10.4254/wjh.v15.i5.675

Full Article (PDF)	WJH-15-675-with-cover.pdf
Full Article (Word)	WJH-15-675.docx
Manuscript File	83748_Auto_Edited-JLW.docx
Answering Reviewers	83748-Answering reviewers.pdf
Audio Core Tip	83748-Audio core tip.m4a
Conflict-of-Interest Disclosure Form	83748-Conflict-of-interest statement.pdf
Copyright License Agreement	83748-Copyright license agreement.pdf
Non-Native Speakers of English Editing Certificate	83748-Language certificate.pdf
Peer-review Report	83748-Peer-review(s).pdf
Scientific Misconduct Check	83748-Bing-Ma YJ-2.jpg
Scientific Editor Work List	83748-Scientific editor work list.pdf
CrossCheck Report	83748-CrossCheck Report.pdf