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Articles Published Processes
3/21/2025 7:11:07 AM | Browse: 153 | Download: 550
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Received |
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2024-08-12 14:37 |
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Peer-Review Started |
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2024-08-12 14:37 |
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First Decision by Editorial Office Director |
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2025-01-03 09:50 |
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Return for Revision |
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2025-01-03 09:50 |
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Revised |
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2025-01-12 18:21 |
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Publication Fee Transferred |
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2025-01-22 07:13 |
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Second Decision by Editor |
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2025-02-18 02:41 |
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Second Decision by Editor-in-Chief |
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Final Decision by Editorial Office Director |
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2025-02-18 10:01 |
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Articles in Press |
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2025-02-18 10:01 |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2025-03-17 01:01 |
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Publish the Manuscript Online |
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2025-03-21 07:11 |
| ISSN |
1949-8462 (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. |
| Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
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| Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
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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 |
Cardiac & Cardiovascular Systems |
| Manuscript Type |
Minireviews |
| Article Title |
Nexilin mutations, a cause of chronic heart failure: A state-of-the-art review starting from a clinical case
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| Manuscript Source |
Unsolicited Manuscript |
| All Author List |
Oana-Cornelia Năstasie, Dan-Andrei Radu, Sebastian Onciul, Marian-Bogdan Drăgoescu and Nicoleta-Monica Popa-Fotea |
| ORCID |
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| Funding Agency and Grant Number |
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| Corresponding Author |
Nicoleta-Monica Popa-Fotea, MD, PhD, Department of Cardiology, Clinical Emergency Hospital, 8 Floreasca Street, Bucharest 014461, Romania. fotea.nicoleta@yahoo.com |
| Key Words |
Heart failure; Genetic cardiomyopathies; Dilated cardiomyopathy; Nexilin gene; G650del nexilin variant |
| Core Tip |
Cardiomyopathies are a leading cause of heart failure, a condition marked by high morbidity and mortality despite continuous advancements in diagnosis and treatment. This review provides a succinct overview of cardiomyopathies, with a particular emphasis on their genetic origins - specifically, nexilin cardiomyopathy - highlighted through the case of a patient diagnosed with this condition. Existing research provides scarce information on individuals carrying nexilin mutations, and the relationship between this gene and cardiomyopathies continues to be actively investigated. |
| Publish Date |
2025-03-21 07:11 |
| Citation |
Năstasie OC, Radu DA, Onciul S, Drăgoescu MB, Popa-Fotea NM. Nexilin mutations, a cause of chronic heart failure: A state-of-the-art review starting from a clinical case. World J Cardiol 2025; 17(3): 100290 |
| URL |
https://www.wjgnet.com/1949-8462/full/v17/i3/100290.htm |
| DOI |
https://dx.doi.org/10.4330/wjc.v17.i3.100290 |
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