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12/19/2024 6:09:11 AM | Browse: 121 | Download: 196
Publication Name World Journal of Clinical Cases
Manuscript ID 100223
Country Croatia
Received
2024-08-10 09:23
Peer-Review Started
2024-08-10 09:23
To Make the First Decision
Return for Revision
2024-10-25 02:58
Revised
2024-11-06 13:31
Second Decision
2024-12-02 02:44
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief
2024-12-02 07:54
Articles in Press
2024-12-02 07:54
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2024-12-11 05:02
Publish the Manuscript Online
2024-12-19 01:57
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/
Copyright © The Author(s) 2025. Published by Baishideng Publishing Group Inc. All rights reserved.
Article Reprints For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website http://www.wjgnet.com
Category Hematology
Manuscript Type Minireviews
Article Title Beta thalassemia syndromes: New insights
Manuscript Source Invited Manuscript
All Author List Ana Dordevic, Ines Mrakovcic-Sutic, Sonja Pavlovic, Milena Ugrin and Jelena Roganovic
Funding Agency and Grant Number
Corresponding Author Jelena Roganovic, MD, PhD, Department of Pediatric Hematology and Oncology, Children’s Hospital Zagreb, Klaiceva 16, Zagreb 10000, Croatia. jelena.roganovic@kdb.hr
Key Words Beta thalassemia; Hemoglobin; Molecular defects; Ineffective erythropoiesis; Hemolysis; Transfusion; Iron chelation; Novel therapies
Core Tip Beta thalassemia syndromes are among the most common monogenic disorders worldwide, characterized by impaired hemoglobin synthesis that leads to ineffective erythropoiesis, chronic hemolysis, iron overload, and subsequent complications. The clinical manifestations are diverse, as a result of the underlying beta-globin gene variants and the coinheritance of modifying factors. Recent advances in the understanding of the underlying molecular and cellular mechanisms have facilitated the development of novel therapeutic strategies. The purpose of this article is to briefly describe new insights in the pathophysiology of this old disease, and discuss revolutionary changes in the treatment landscape for severe forms of beta thalassemia.
Publish Date 2024-12-19 01:57
Citation <p>Dordevic A, Mrakovcic-Sutic I, Pavlovic S, Ugrin M, Roganovic J. Beta thalassemia syndromes: New insights. <i>World J Clin Cases</i> 2025; 13(10): 100223</p>
URL https://www.wjgnet.com/2307-8960/full/v13/i10/100223.htm
DOI https://dx.doi.org/10.12998/wjcc.v13.i10.100223
Full Article (PDF) WJCC-13-100223-with-cover.pdf
Manuscript File 100223_Auto_Edited_020402.docx
Answering Reviewers 100223-answering-reviewers.pdf
Audio Core Tip 100223-audio.m4a
Conflict-of-Interest Disclosure Form 100223-conflict-of-interest-statement.pdf
Copyright License Agreement 100223-copyright-assignment.pdf
Non-Native Speakers of English Editing Certificate 100223-non-native-speakers.pdf
Peer-review Report 100223-peer-reviews.pdf
Scientific Misconduct Check 100223-scientific-misconduct-check.png
Scientific Editor Work List 100223-scientific-editor-work-list.pdf
CrossCheck Report 100223-crosscheck-report.pdf