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12/19/2024 6:09:12 AM | Browse: 147 | Download: 253
Publication Name World Journal of Clinical Cases
Manuscript ID 98390
Country China
Received
2024-06-25 10:29
Peer-Review Started
2024-06-25 10:29
To Make the First Decision
Return for Revision
2024-10-17 07:55
Revised
2024-10-29 14:45
Second Decision
2024-12-05 02:38
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief
2024-12-05 09:23
Articles in Press
2024-12-05 09:23
Publication Fee Transferred
2024-11-04 04:45
Edit the Manuscript by Language Editor
Typeset the Manuscript
2024-12-08 04:55
Publish the Manuscript Online
2024-12-19 01:57
ISSN 2307-8960 (online)
Open Access 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/
Copyright © The Author(s) 2025. Published by Baishideng Publishing Group Inc. All rights reserved.
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Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Genetics & Heredity
Manuscript Type Case Report
Article Title Systemic thrombosis with prothrombin Belgrade mutation in a Chinese patient: A case report
Manuscript Source Unsolicited Manuscript
All Author List Yan-Feng Wu, Yan Huang, Bao-Hui Weng, Shan Deng, Li-Ya Pan and Zhen Li
Funding Agency and Grant Number
Corresponding Author Zhen Li, MD, Department of Neurology, Tianjin Medical University General Hospital, No. 154 Anshan Road, Tianjin 300052, China. lzz_tmu@163.com
Key Words Arg596Gln; Belgrade mutation; Thrombophilia; Prothrombin; Case report
Core Tip The aim of our present study is to display a novel missense mutation in the prothrombin gene (p.Arg596Gln) in a Chinese patient with onset of cerebral venous thrombosis. Considering that prothrombin Belgrade mutation mechanism and treatment are still not fully elucidated, we provide the understanding about hereditary risk factors of cerebral venous thrombosis and triggers the further exploration of effective and exact therapeutic options and management on cerebral venous thrombosis caused by prothrombin Belgrade mutation.
Publish Date 2024-12-19 01:57
Citation <p>Wu YF, Huang Y, Weng BH, Deng S, Pan LY, Li Z. Systemic thrombosis with prothrombin Belgrade mutation in a Chinese patient: A case report. <i>World J Clin Cases</i> 2025; 13(10): 98390</p>
URL https://www.wjgnet.com/2307-8960/full/v13/i10/98390.htm
DOI https://dx.doi.org/10.12998/wjcc.v13.i10.98390
Full Article (PDF) WJCC-13-98390-with-cover.pdf
CARE Checklist–2016 98390-CARE-Checklist-2016.pdf
Manuscript File 98390_Auto_Edited_004437.docx
Answering Reviewers 98390-answering-reviewers.pdf
Audio Core Tip 98390-audio.mp3
Conflict-of-Interest Disclosure Form 98390-conflict-of-interest-statement.pdf
Copyright License Agreement 98390-copyright-assignment.pdf
Signed Consent for Treatment Form(s) or Document(s) 98390-informed-consent-statement.pdf
Non-Native Speakers of English Editing Certificate 98390-non-native-speakers.pdf
Peer-review Report 98390-peer-reviews.pdf
Scientific Misconduct Check 98390-scientific-misconduct-check.png
Scientific Editor Work List 98390-scientific-editor-work-list.pdf
CrossCheck Report 98390-crosscheck-report.pdf