Correction to: Comprehensive genetic characteristics of dystrophinopathies in China.
作者信息
Ma Peipei, Zhang Shu, Zhang Hao, Fang Siying, Dong Yuru, Zhang Yan, Hao Weiwei, Wu Shiwen, Zhao Yuying
机构信息
Department of Neurology, the General Hospital of Chinese People's Armed Police Force, Beijing, China.
Department of Magnetic Resonance, the General Hospital of Chinese People's Armed Police Force, Beijing, China.
出版信息
Orphanet J Rare Dis. 2021 Jun 2;16(1):252. doi: 10.1186/s13023-021-01853-x.
Abstract
摘要
相似文献
1
Correction to: Comprehensive genetic characteristics of dystrophinopathies in China.对《中国肌营养不良症的综合遗传特征》的更正
Orphanet J Rare Dis. 2021 Jun 2;16(1):252. doi: 10.1186/s13023-021-01853-x.
2
Comprehensive genetic characteristics of dystrophinopathies in China.中国肌营养不良症的综合遗传特征。
Orphanet J Rare Dis. 2018 Jul 4;13(1):109. doi: 10.1186/s13023-018-0853-z.
3
Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan.日本肌营养不良症的基因诊断综合分析。
Orphanet J Rare Dis. 2017 Aug 31;12(1):149. doi: 10.1186/s13023-017-0703-4.
4
[Improvements in the diagnosis of dystrophinopathies: what have we learnt in these last 20 years?].[杜兴氏肌营养不良症诊断的进展：过去20年我们学到了什么？]
Rev Neurol. 2011 Feb 16;52(4):239-49.
5
The Dystrophinopathies.肌营养不良症
Continuum (Minneap Minn). 2019 Dec;25(6):1619-1639. doi: 10.1212/CON.0000000000000791.
6
A deep learning model for diagnosing dystrophinopathies on thigh muscle MRI images.一种用于在大腿肌肉MRI图像上诊断肌营养不良症的深度学习模型。
BMC Neurol. 2021 Jan 11;21(1):13. doi: 10.1186/s12883-020-02036-0.
7
The trefoil with single fruit sign in muscle magnetic resonance imaging is highly specific for dystrophinopathies.肌肉磁共振成像中的单果实三叶形征对肌营养不良蛋白病具有高度特异性。
Eur J Radiol. 2015 Oct;84(10):1992-8. doi: 10.1016/j.ejrad.2015.06.011. Epub 2015 Jun 18.
8
Genotypes and Phenotypes of Small Mutations in Chinese Patients With Dystrophinopathies.中国肌营养不良症患者微小突变的基因型与表型
Front Genet. 2019 Feb 18;10:114. doi: 10.3389/fgene.2019.00114. eCollection 2019.
9
Dystrophinopathies.肌营养不良症
Semin Neurol. 2015 Aug;35(4):369-84. doi: 10.1055/s-0035-1558982. Epub 2015 Oct 6.
10
Autism spectrum disorders are prevalent among patients with dystrophinopathies.自闭症谱系障碍在肌营养不良症患者中较为常见。
Neurol Sci. 2018 Jul;39(7):1279-1282. doi: 10.1007/s10072-018-3341-2. Epub 2018 Mar 28.
本文引用的文献
1
Comprehensive genetic characteristics of dystrophinopathies in China.中国肌营养不良症的综合遗传特征。
Orphanet J Rare Dis. 2018 Jul 4;13(1):109. doi: 10.1186/s13023-018-0853-z.
Zotero 插件