Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Hao-Ling Xu"'
Autor:
Xin-Yuan Chen, Yan-Hua Lian, Xia-Hua Liu, Arif Sikandar, Meng-Cheng Li, Hao-Ling Xu, Jian-Ping Hu, Qun-Lin Chen, Shi-Rui Gan
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2022)
BackgroundSpinocerebellar ataxia type 3 (SCA3) is the most common autosomal dominant hereditary ataxia, and, thus far, effective treatment remains low. Repetitive transcranial magnetic stimulation (rTMS) can improve the symptoms of spinal cerebellar
Externí odkaz:
https://doaj.org/article/3567ed4a6c404b37966fffb5d88c7bc8
Autor:
Xia‐Hua Liu, Ying Li, Hao‐Ling Xu, Arif Sikandar, Wei‐Hong Lin, Gui‐He Li, Xiao‐Fen Li, Alimire Alimu, Sheng‐Bin Yu, Xiang‐Hui Ye, Ning Wang, Jun Ni, Wan‐Jin Chen, Shi‐Rui Gan
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 8, Pp 1360-1370 (2020)
Abstract Objective Spinocerebellar ataxia type 3 (SCA3) is one of the most common hereditary neurodegenerative diseases, with balance instability as main symptom. Balance quantification is crucial for evaluating the efficacy of therapeutic interventi
Externí odkaz:
https://doaj.org/article/2fb0f08aba074341bb460885115ef3ec
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
BackgroundSpinocerebellar ataxia type 3 (SCA3) is one of the most common hereditary neurodegenerative diseases. Postural control dysfunction is the main symptom of SCA3, and the proprioceptive system is a critical sensory component of postural contro
Externí odkaz:
https://doaj.org/article/5cf4a0aeb8c546ccb30edaefe40062ec
Autor:
Jin-Shan Yang, Hao-Ling Xu, Ping-Ping Chen, Arif Sikandar, Mei-Zhen Qian, Hui-Xia Lin, Min-Ting Lin, Wan-Jin Chen, Ning Wang, Hua Wu, Shi-Rui Gan
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Background: Spinocerebellar ataxia type 3 (SCA3) is an inherited form of ataxia that leads to progressive neurodegeneration. Fatigue is a common non-motor symptom in SCA3 and other neurodegenerative diseases, such as Parkinson's disease (PD) and amyo
Externí odkaz:
https://doaj.org/article/cd5a74f912dd44feb92786838e3a0484
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
Publikováno v:
Shanghai Jiaotong Daxue xuebao, Vol 58, Iss 9, Pp 1334-1343 (2024)
The quantitative evaluation of the uncertainty in distributed photovoltaic power is significant for the safe and stable operation of distribution network. Considering the significant differences in power characteristics of different output fluctuatio
Externí odkaz:
https://doaj.org/article/4339b8f2add24ee4807c6c00d785b888
Autor:
Zhi-Xian Ye, Hao-Ling Xu, Na-Ping Chen, Xin-Yuan Chen, Meng-Cheng Li, Ru-Ying Yuan, Wei Lin, Liangliang Qiu, Minting Lin, Wan-Jin Chen, Ning Wang, Jian-Ping Hu, Ying Fu, Shi-Rui Gan
Publikováno v:
Neurology: Genetics; Jun2024, Vol. 10 Issue 3, p1-9, 9p
Autor:
Hao-Ling Xu, Jianping Hu, Yuqing Tu, Dairong Cao, Xinyuan Chen, Qun-Lin Chen, Shirui Gan, Mengcheng Li, Naping Chen, Ziqiang Huang
Publikováno v:
Brain Imaging and Behavior. 16:379-388
Spinocerebellar ataxias type 3 (SCA3) patients are clinically characterized by progressive cerebellar ataxia combined with degeneration of the cerebellum. Previous neuroimaging studies have indicated ataxia severity associated with cerebellar atrophy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d88e0a22301987135797bd947df531e6
https://doi.org/10.1007/s11682-021-00511-x
https://doi.org/10.1007/s11682-021-00511-x
Autor:
Alimire Alimu, Wan-Jin Chen, Hao-Ling Xu, Shi-Rui Gan, Sheng‐Bin Yu, Xiao‐Fen Li, Wei-Hong Lin, Arif Sikandar, Jun Ni, Xiang‐Hui Ye, Ying Li, Ning Wang, Xia-Hua Liu, Gui-He Li
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 8, Pp 1360-1370 (2020)
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology
Objective Spinocerebellar ataxia type 3 (SCA3) is one of the most common hereditary neurodegenerative diseases, with balance instability as main symptom. Balance quantification is crucial for evaluating the efficacy of therapeutic interventions. Howe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdd0d915a7f5e8fb3f74b8931c35ae8b
https://doaj.org/article/2fb0f08aba074341bb460885115ef3ec
https://doaj.org/article/2fb0f08aba074341bb460885115ef3ec
Autor:
Arif Sikandar, Xia-Hua Liu, Hao-Ling Xu, Ying Li, Yun-Qing Lin, Xin-Yuan Chen, Gui-He Li, Min-Ting Lin, Ning Wang, Wan-Jin Chen, Guo-Xin Ni, Shi-Rui Gan
Publikováno v:
Parkinsonism & Related Disorders. 106:105236
Spinocerebellar ataxia type 3 (SCA3) is the most common autosomal dominant ataxia globally. No effective treatment is currently available for SCA3. Repetitive Transcranial Magnetic Stimulation (rTMS) is a non-invasive form of brain stimulation, demon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::915ae045f9fa8613879f1c4a31282ad8
https://doi.org/10.1016/j.parkreldis.2022.105236
https://doi.org/10.1016/j.parkreldis.2022.105236