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Articles Published Processes
1/18/2022 2:50:51 AM | Browse: 325 | Download: 811
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Received |
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2021-02-28 10:59 |
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Peer-Review Started |
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2021-02-28 11:14 |
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To Make the First Decision |
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Return for Revision |
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2021-09-05 21:24 |
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Revised |
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2021-09-25 23:15 |
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Second Decision |
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2021-12-01 03:21 |
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Accepted by Journal Editor-in-Chief |
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Accepted by Executive Editor-in-Chief |
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2021-12-02 01:55 |
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Articles in Press |
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2021-12-02 01:55 |
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Publication Fee Transferred |
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Edit the Manuscript by Language Editor |
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Typeset the Manuscript |
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2021-12-31 02:51 |
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Publish the Manuscript Online |
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2022-01-18 02:50 |
ISSN |
2220-3206 (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) 2022. 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 |
Neurosciences |
Manuscript Type |
Minireviews |
Article Title |
Molecular typing of familial temporal lobe epilepsy
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Manuscript Source |
Invited Manuscript |
All Author List |
Chao Liu, Xiao-Zhi Qiao, Zi-Han Wei, Mi Cao, Zhen-Yu Wu and Yan-Chun Deng |
ORCID |
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Funding Agency and Grant Number |
Funding Agency |
Grant Number |
National Key R&D Program of China, Precision medicine program——Cohort study on nervous system diseases |
2017YFC0907702 |
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Corresponding Author |
Yan-Chun Deng, MD, PhD, Chief Doctor, Professor, Neurology, The First Affiliated Hospital of Air Force Medical University, China, Xi'an/710032, No.127,Changle West Road, Xi'an 710032, China. yanchund@fmmu.edu.cn |
Key Words |
Temporal lobe epilepsy; Gene mutation; Gene locus; Phenotypes; Prognosis |
Core Tip |
Eleven types of familial temporal lobe epilepsy (FTLE) caused by single gene mutations or specific gene loci had been identified to date. The phenotype of FTLE was heterogenous and includes typical temporal lobe seizures and specific symptoms. We herein describe the etiology, inheritance, phenotype and prognosis of each type of FTLE and summarize their similarities and differences. |
Publish Date |
2022-01-18 02:50 |
Citation |
Liu C, Qiao XZ, Wei ZH, Cao M, Wu ZY, Deng YC. Molecular typing of familial temporal lobe epilepsy. World J Psychiatr 2022; 12(1): 98-107 |
URL |
https://www.wjgnet.com/2220-3206/full/v12/i1/98.htm |
DOI |
https://dx.doi.org/10.5498/wjp.v12.i1.98 |
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