Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Xian-Jin Shang"'
Publikováno v:
Dermatology and Therapy, Vol 10, Iss 2, Pp 273-283 (2020)
Abstract Introduction Many studies have explored the imaging characteristics of patients with neurosyphilis, but no systematic study has been made on the neuroimaging changes after anti-syphilitic treatment. The purpose of this study was to examine n
Externí odkaz:
https://doaj.org/article/5effcdecf09e4fb997e168daec855431
Autor:
Xian-Jin Shang, Zhong-Hua Shi, Cai-Feng He, Shuai Zhang, Yong-Jie Bai, Yong-Tao Guo, Bo Sun, Shun Li, Huai-Ming Wang, Zhi-Ming Zhou, Wen-Jie Zi, Xin-Feng Liu
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-7 (2019)
Abstract Background Mechanical thrombectomy has been proven as a standard care for moderate to severe ischemic stroke with anterior large vessel occlusion (LVO); however, whether it is equally effective in mild ischemic stroke (MIS) is controversial.
Externí odkaz:
https://doaj.org/article/de9058434e684ba392cef0345c9eea8f
Autor:
Hao‐Ling Xu, Qiu‐Ni Su, Xian‐Jin Shang, Arif Sikandar, Min‐Ting Lin, Ning Wang, Hong Lin, Shi‐Rui Gan
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 7, Pp n/a-n/a (2019)
Abstract Background Spinocerebellar ataxia type 3 (SCA3) is a rare, inherited form of ataxia that leads to progressive neurodegeneration. The initial symptoms could affect clinical phenotypes in neurodegenerative diseases, such as Parkinson's disease
Externí odkaz:
https://doaj.org/article/358f2f74a5d44eb8b3433e60fadf2f77
Autor:
Min Ting Lin, Xian Jin Shang, Shi Rui Gan, Hao Ling Xu, Arif Sikandar, Qiu Ni Su, Ning Wang, Hong Lin
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 7, Iss 7, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicine, Vol 7, Iss 7, Pp n/a-n/a (2019)
Background Spinocerebellar ataxia type 3 (SCA3) is a rare, inherited form of ataxia that leads to progressive neurodegeneration. The initial symptoms could affect clinical phenotypes in neurodegenerative diseases, such as Parkinson's disease and amyo
Autor:
Xian-Jin Shang, Bin Jiang, Dan-Ni Wang, Ning Wang, Yu-Chao Chen, Yi-Jun Chen, Shi-Rui Gan, Wan-Jin Chen, Hui-Xia Lin, Min-Ting Lin, Ping-Ping Chen, Mei-Zhen Qian, Jin-Shan Yang, Xiao-Ping Chen
Publikováno v:
Cerebellum (London, England). 17(4)
Spinocerebellar ataxia type 3 (SCA3), the most common subtype of SCA worldwide, is caused by mutation of CAG repeats expansion in ATXN3. Body mass index (BMI) is an important modulatory factor in the progression of neurodegenerative disorders such as
Autor:
Min-Ting Lin, Wan-Jin Chen, Xiao-Ping Chen, Yi-Jun Chen, Bin Jiang, Shi-Rui Gan, Yu-Chao Chen, Ning Wang, Mei-Zhen Qian, Hui-Xia Lin, Hao-Ling Xu, Zhi-Ming Zhou, Jin-Shan Yang, Xian-Jin Shang, Ping-Ping Chen
Publikováno v:
Journal of the neurological sciences. 390
Background Spinocerebellar ataxia type 3 (SCA3) is the most common subtype of SCAs worldwide. SCA3 homozygote is defined as expanded CAG repeats in both alleles that might exhibit severe phenotype due to gene dosage effect. However, a study on the sy
Autor:
Xiao-Ping Chen, Xian-Jin Shang, Wan-Jin Chen, Ping-Ping Chen, Yi-Jun Chen, Yu-Chao Chen, Mei-Zhen Qian, Ning Wang, Hui-Xia Lin, Dan-Ni Wang, Bin Jiang, Min-Ting Lin, Jin-Shan Yang, Shi-Rui Gan
Publikováno v:
European neurology. 79(5-6)
Background: Spinocerebellar ataxia type 3 (SCA3), which is the most common subtype of SCA worldwide, exhibits common neuropsychological symptoms such as depression. However, the contribution of depression to the severity of SCA3 has not yet been thor