Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yu‐Sen Qiu"'
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
Autor:
Xiang Lin, Ying Liu, Yi Lin, Ning Wang, Wan-Jin Chen, Ying Fu, Xiao-Hong Lin, Yu-Sen Qiu, Yi-Heng Zeng, Ru-Ying Yuan, Zhi-Xian Ye, Jin Bi, Yi-Jun Chen, Meng-Wen Wang, Shao-Bo Yao, Yi-Kun Chen, Jun-Yi Jiang
Publikováno v:
BMJ Open, Vol 12, Iss 1 (2022)
Externí odkaz:
https://doaj.org/article/890f122e4ee44fa99d8268965612cc9d
Autor:
Yi-Jun Chen, Zai-Qiang Zhang, Meng-Wen Wang, Yu-Sen Qiu, Ru-Ying Yuan, En-Lin Dong, Zhe Zhao, Hai-Tao Zhou, Ning Wang, Wan-Jin Chen, Xiang Lin
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Background: Hereditary spastic paraplegia (HSP) caused by mutations in ALDH18A1 have been reported as spastic paraplegia 9 (SPG9), with autosomal dominant and autosomal recessive transmission (SPG9A and SPG9B). SPG9 is rare and has shown phenotypic a
Externí odkaz:
https://doaj.org/article/a9dadbf104b14aa7bf34237945e355bf
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
https://doi.org/10.1002/acn3.51713
Autor:
Yi‐Heng Zeng, Kang Yang, Gan‐Qin Du, Yi‐Kun Chen, Chun‐Yan Cao, Yu‐Sen Qiu, Jin He, Hai‐Dong Lv, Qian‐Qian Qu, Jian‐Nan Chen, Guo‐Rong Xu, Long Chen, Fu‐Ze Zheng, Miao Zhao, Min‐Ting Lin, Wan‐Jin Chen, Jing Hu, Zhi‐Qiang Wang, Ning Wang
Publikováno v:
Annals of Neurology. 92:512-526
Oculopharyngodistal myopathy (OPDM) is an adult-onset neuromuscular disease characterized by progressive ptosis, dysarthria, ophthalmoplegia, and distal muscle weakness. Recent studies revealed that GGC repeat expansions in 5'-UTR of LRP12, GIPC1, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd83a57931a3880691cc67a60eed3ee9
https://doi.org/10.1002/ana.26436
https://doi.org/10.1002/ana.26436
Autor:
Yi-Jun, Chen, Zai-Qiang, Zhang, Meng-Wen, Wang, Yu-Sen, Qiu, Ru-Ying, Yuan, En-Lin, Dong, Zhe, Zhao, Hai-Tao, Zhou, Ning, Wang, Wan-Jin, Chen, Xiang, Lin
Publikováno v:
Frontiers in Neurology
Background: Hereditary spastic paraplegia (HSP) caused by mutations in ALDH18A1 have been reported as spastic paraplegia 9 (SPG9), with autosomal dominant and autosomal recessive transmission (SPG9A and SPG9B). SPG9 is rare and has shown phenotypic a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2502de1eb6b12a8644abc574f83be4a7
https://pubmed.ncbi.nlm.nih.gov/34093392
https://pubmed.ncbi.nlm.nih.gov/34093392
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)
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
https://doi.org/10.1136/bmjopen-2021-054011