Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Dongyue Yue"'
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
ObjectivesThis study aimed to assess the feasibility of a machine learning-based radiomics tools to discriminate between Limb-girdle muscular dystrophy R2 (LGMDR2) and immune-mediated necrotizing myopathy (IMNM) using lower-limb muscle magnetic reson
Externí odkaz:
https://doaj.org/article/c487971b4ea5441cb4c90de83ec2ff00
Autor:
Kexin Jiao, Dongyue Yue, Xinyu Gu, Nachuan Cheng, Xuechun Chang, Huahua Zhong, Xiao Huan, Manqiqige Su, Yufan Zhou, Sushan Luo, Chongbo Zhao, Jianying Xi, Wenhua Zhu
Publikováno v:
Stem Cell Research, Vol 64, Iss , Pp 102897- (2022)
Oculopharyngodistal myopathy (OPDM) is a late-onset degenerative muscle disorder characterized by ptosis and weakening of the facial, pharyngeal, and distal limb muscles. Our study reprogrammed human-induced pluripotent stem cells (iPSC) from the per
Externí odkaz:
https://doaj.org/article/febb7cdc98084f5eaeeb7bec42757f04
Autor:
Kexin Jiao, Jihong Dong, Sushan Luo, Liqiang Yu, Qing Ke, Zhiqiang Wang, Xinghua Luan, Xiaojie Zhang, Junhong Guo, Yan Chen, Xihua Li, Song Tan, Fangyuan Qian, Jianming Jiang, Xuen Yu, Dongyue Yue, Changxia Liu, Lijun Luo, Jianping Li, Yanzhou Qu, Lan Chen, Jianglong Tu, Chong Sun, Chong Yan, Jie Song, Jianying Xi, Jie Lin, Jiahong Lu, Chongbo Zhao, Wenhua Zhu, Qi Fang
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
IntroductionThe lack of knowledge regarding the differences between Chinese and other ethnicities in the early manifestation of late-onset Pompe disease (LOPD) prohibits the development of an effective screening strategy. We conducted a multicenter s
Externí odkaz:
https://doaj.org/article/83bc4ce35aba41e78a0aec065305079a
Autor:
Xinyu Gu, Jiaxi Yu, Kexin Jiao, Jianwen Deng, Xingyu Xia, Kai Qiao, Dongyue Yue, Mingshi Gao, Chongbo Zhao, Jihong Dong, Gongchun Huang, Jingli Shan, Chuanzhu Yan, Li Di, Yuwei Da, Wenhua Zhu, Jianying Xi, Zhaoxia Wang
Publikováno v:
Journal of Medical Genetics; Apr2024, Vol. 61 Issue 4, p340-346, 15p
Publikováno v:
Muscle & Nerve. 67
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3662688a15ae7d3b2d4dfba68c55812
https://doi.org/10.1002/mus.27808
https://doi.org/10.1002/mus.27808
Autor:
Jiahong Lu, Sushan Luo, Yan Zhou, Zonghui Liang, Ailian Du, Jun Lu, Dongyue Yue, Jie Yang, Chongbo Zhao, Jihong Dong, Lijun Luo, Yan Chen, Wang Xilu, Jing Li, Wenbo Yu, Qunfeng Wu, Zhenmin Niu, Yiqi Liu, Wenhua Zhu, Jie Lin, Kai Qiao, Jianying Xi, Tonghai Dou
Publikováno v:
Brain. 144:601-614
Oculopharyngodistal myopathy is a late-onset degenerative muscle disorder characterized by ptosis and weakness of the facial, pharyngeal, and distal limb muscles. A recent report suggested a non-coding trinucleotide repeat expansion in LRP12 to be as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4763ea396f09f21c4381c070696b923
https://doi.org/10.1093/brain/awaa426
https://doi.org/10.1093/brain/awaa426
Autor:
Changxia Liu, Dongyue Yue, Xuelin Feng, Chong Sun, Sushan Luo, Jing Li, Wenhua Zhu, Jiahong Lu, Zonghui Liang, Jianying Xi
Publikováno v:
Journal of Clinical Neuroscience. 81:259-264
Introduction Impaired mood and quality of life was common in muscular dystrophies and play an important role in long-term management. Previous studies in dysferlinopathies mainly focused on the genotype-phenotypes correlations. Currently there are ve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a8b0d03e589bc77c4ad80ecc10b0b91
https://doi.org/10.1016/j.jocn.2020.09.069
https://doi.org/10.1016/j.jocn.2020.09.069
Autor:
Chong Yan, Jie Lin, Jianping Li, Yan Chen, Jianying Xi, Xihua Li, Qing Ke, Fangyuan Qian, Wenhua Zhu, Zhiqiang Wang, Chong Sun, Jie Song, Changxia Liu, Yanzhou Qu, Jihong Dong, Jianglong Tu, Junhong Guo, Xinghua Luan, Jianming Jiang, Qi Fang, Chongbo Zhao, Lan Chen, Xiaojie Zhang, Liqiang Yu, Kexin Jiao, Lijun Luo, Dongyue Yue, Jiahong Lu, Song Tan, Sushan Luo, Xuen Yu
Backgroud: Pompe disease is a rare metabolic disorder with available enzymatic replacement therapy. Contrasting with the classic infantile form, the others subtypes have a heterogeneous presentation that makes an early and accurate diagnosis difficul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a91bc845e7100772e6987c532a93a6d
https://doi.org/10.21203/rs.3.rs-1104428/v1
https://doi.org/10.21203/rs.3.rs-1104428/v1
Autor:
Yiqi Liu, Chongbo Zhao, Hui Wu, Jianying Xi, Wenhua Zhu, L. Zhou, Jie Lin, Dongyue Yue, Kai Qiao, Jiahong Lu
Publikováno v:
Journal of Clinical Neuroscience. 65:41-45
In order to describe the clinical characteristics, treatment response and long-term follow up in Lambert–Eaton myasthenic syndrome (LEMS) patients with and without small cell lung cancer (SCLC) in East China, patients seen in Huashan Hospital from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26322caa84dd416658b3df5bb6b7096f
https://doi.org/10.1016/j.jocn.2019.04.003
https://doi.org/10.1016/j.jocn.2019.04.003
Autor:
Chongbo Zhao, Wenhua Zhu, Xinfang Gao, Xueni Guan, Jing Li, Jiahong Lu, Zonghui Liang, Dongyue Yue, Jianying Xi, Xuelin Feng, Sushan Luo
Publikováno v:
Muscle & Nerve. 58:536-541
Introduction Limb-girdle muscular dystrophy type 2A (LGMD2A) is characterized by progressive wasting of muscles for which the disease-monitoring tools are still deficient. Methods We performed muscle MRI of the lower limbs in 32 LGMD2A patients and 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e998777cd125e4981a4f76152c24be6c
https://doi.org/10.1002/mus.26169
https://doi.org/10.1002/mus.26169