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7/12/2021 1:19:31 PM | Browse: 233 | Download: 439
Publication Name World Journal of Meta-Analysis
Manuscript ID 61346
Country India
Received
2020-12-03 08:15
Peer-Review Started
2020-12-03 08:15
To Make the First Decision
Return for Revision
2021-05-06 06:00
Revised
2021-05-20 06:40
Second Decision
2021-06-17 12:24
Accepted by Journal Editor-in-Chief
Accepted by Company Editor-in-Chief
2021-06-17 12:43
Articles in Press
2021-06-17 12:43
Publication Fee Transferred
Edit the Manuscript by Language Editor
2021-06-21 01:00
Typeset the Manuscript
2021-06-27 14:46
Publish the Manuscript Online
2021-07-12 10:23
ISSN 2308-3840 (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) 2021. 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 Neurosciences
Manuscript Type Minireviews
Article Title Nusinersen, an exon 7 inclusion drug for spinal muscular atrophy: A minireview
Manuscript Source Unsolicited Manuscript
All Author List Bijaylaxmi Behera
Funding Agency and Grant Number
Corresponding Author Bijaylaxmi Behera, MBBS, MD, Chief Physician, Department of Neonatology, Chaitanya Hospital, Sector 44, Chandigarh 160044, India. jollybubu2008@gmail.com
Key Words CHERISH; Nusinersen; Spinal muscular atrophy; Survival motor neuron; NURTURE
Core Tip Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease, with incidence of 1 in 5000 to 1 in 10000 live births. This review provides an elaborative knowledge regarding the current most effective drug for SMA, Nusinersen. A brief discussion on other treatment modalities that are under trials is also provided.
Publish Date 2021-07-12 10:23
Citation Behera B. Nusinersen, an exon 7 inclusion drug for spinal muscular atrophy: A minireview. World J Meta-Anal 2021; 9(3): 277-285
URL https://www.wjgnet.com/2308-3840/full/v9/i3/277.htm
DOI https://dx.doi.org/10.13105/wjma.v9.i3.277
Full Article (PDF) WJMA-9-277.pdf
Full Article (Word) WJMA-9-277.docx
Manuscript File 61346-Review-FilipodiaCL.docx
Answering Reviewers 61346-Answering reviewers.pdf
Audio Core Tip 61346-Audio core tip.aac
Conflict-of-Interest Disclosure Form 61346-Conflict-of-interest statement.pdf
Copyright License Agreement 61346-Copyright license agreement.pdf
Non-Native Speakers of English Editing Certificate 61346-Language certificate.pdf
Peer-review Report 61346-Peer-review(s).pdf
Scientific Misconduct Check 61346-Scientific misconduct check.pdf
Scientific Editor Work List 61346-Scientific editor work list.pdf