Zobrazeno 1 - 10 of 14 pro vyhledávání: '"Zhi‐Xian Ye"'
1
Akademický článek
Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients
Autor: Feng Lin, Kang Yang, Xin Lin, Ming Jin, Long Chen, Fu-ze Zheng, Liang-liang Qiu, Zhi-xian Ye, Hai-zhu Chen, Min-ting Lin, Ning Wang, Zhi-qiang Wang
Publikováno v: Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-18 (2023)
Abstract Background Limb-girdle muscular dystrophies (LGMDs) are a group of heterogeneous inherited diseases predominantly characterized by limb-girdle muscle weakness and dystrophic changes on histological analysis. The frequency of LGMD subtypes va
Externí odkaz: https://doaj.org/article/80189a10ec2d46fb8dda201e21e194aa
Zobrazit plný text záznamu
2
Akademický článek
The phenotypic and genotypic features of Chinese patients with oculopharyngeal muscular dystrophy
Autor: Feng Lin, Kang Yang, Min‐ting Lin, Fu‐ze Zheng, Long Chen, Yuan‐liang Ding, Zhi‐xian Ye, Xin Lin, Ning Wang, Zhi‐qiang Wang
Publikováno v: Annals of Clinical and Translational Neurology, Vol 10, Iss 3, Pp 426-439 (2023)
Abstract Objective Oculopharyngeal muscular dystrophy (OPMD) is a late‐onset inherited neuromuscular disorder, with progressive ptosis and dysphagia as common manifestations. To date, OPMD has rarely been reported among East Asians. The present stu
Externí odkaz: https://doaj.org/article/b8c0cd27b3f74d078e647da2b7a48d2d
Zobrazit plný text záznamu
3
Akademický článek
Altered brain white matter structural motor network in spinocerebellar ataxia type 3
Autor: Xin‐Yuan Chen, Zi‐Qiang Huang, Wei Lin, Meng‐Cheng Li, Zhi‐Xian Ye, Yu‐Sen Qiu, Xiao‐Yue Xia, Na‐Ping Chen, Jian‐Ping Hu, Shi‐Rui Gan, Qun‐Lin Chen
Publikováno v: Annals of Clinical and Translational Neurology, Vol 10, Iss 2, Pp 225-236 (2023)
Abstract Objectives Spinocerebellar ataxia type 3 is a disorder within the brain network. However, the relationship between the brain network and disease severity is still unclear. This study aims to investigate changes in the white matter (WM) struc
Externí odkaz: https://doaj.org/article/e483d362db934e1ab86a34a13cb37bf8
Zobrazit plný text záznamu
8
Altered brain white matter structural motor network in spinocerebellar ataxia type 3
Autor: Xin‐Yuan Chen, Zi‐Qiang Huang, Wei Lin, Meng‐Cheng Li, Zhi‐Xian Ye, Yu‐Sen Qiu, Xiao‐Yue Xia, Na‐Ping Chen, Jian‐Ping Hu, Shi‐Rui Gan, Qun‐Lin Chen
Publikováno v: Annals of Clinical and Translational Neurology. 10:225-236
Spinocerebellar ataxia type 3 is a disorder within the brain network. However, the relationship between the brain network and disease severity is still unclear. This study aims to investigate changes in the white matter (WM) structural motor network,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae90b75840fef3711ccf0488d7291f2e
https://doi.org/10.1002/acn3.51713
Zobrazit plný text záznamu
9
Chinese patients with hereditary spastic paraplegias (HSPs): a protocol for a hospital-based cohort study
Autor: Yu-Sen Qiu, Yi-Heng Zeng, Ru-Ying Yuan, Zhi-Xian Ye, Jin Bi, Xiao-Hong Lin, Yi-Jun Chen, Meng-Wen Wang, Ying Liu, Shao-Bo Yao, Yi-Kun Chen, Jun-Yi Jiang, Yi Lin, Xiang Lin, Ning Wang, Ying Fu, Wan-Jin Chen
Publikováno v: BMJ Open
BMJ Open, Vol 12, Iss 1 (2022)
IntroductionHereditary spastic paraplegias (HSPs) are uncommon but not rare neurodegenerative diseases. More than 100 pathogenic genes and loci related to spastic paraplegia symptoms have been reported. HSPs have the same core clinical features, incl
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::424f7b9f220b66a79a87b2349a37767f
https://doi.org/10.1136/bmjopen-2021-054011
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje