Zobrazeno 1 - 10
of 504
pro vyhledávání: '"Linlin Wan"'
Autor:
Sudan Zhu, Yuting Shi, Zhao Chen, Zhe Long, Linlin Wan, Daji Chen, Xinrong Yuan, You Fu, Feiyan Deng, Xiafei Long, Kefang Du, Rong Qiu, Beisha Tang, Chunrong Wang, Hong Jiang
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 8, Pp 2100-2111 (2024)
Abstract Objective Transcranial sonography (TCS) is a noninvasive neuroimaging technique, visualizing deep brain structures and the ventricular system. Although widely employed in diagnosing various movement disorders, such as Parkinson's disease and
Externí odkaz:
https://doaj.org/article/3a8c5057010f435d81054bfcd997773b
Publikováno v:
BioMedical Engineering OnLine, Vol 23, Iss 1, Pp 1-20 (2024)
Abstract Background Transcranial sonography (TCS) plays a crucial role in diagnosing Parkinson's disease. However, the intricate nature of TCS pathological features, the lack of consistent diagnostic criteria, and the dependence on physicians' expert
Externí odkaz:
https://doaj.org/article/3dfa5b8b2cf6486b92fb6132cc506af5
Autor:
Riwei Ouyang, Linlin Wan, David Pellerin, Zhe Long, Jian Hu, Qian Jiang, Chunrong Wang, Linliu Peng, Huirong Peng, Lang He, Rong Qiu, Junling Wang, Jifeng Guo, Lu Shen, Bernard Brais, Matt C. Danzi, Stephan Zuchner, Beisha Tang, Zhao Chen, Hong Jiang
Publikováno v:
EBioMedicine, Vol 102, Iss , Pp 105077- (2024)
Summary: Background: An intronic GAA repeat expansion in FGF14 was recently identified as a cause of GAA-FGF14 ataxia. We aimed to characterise the frequency and phenotypic profile of GAA-FGF14 ataxia in a large Chinese ataxia cohort. Methods: A tota
Externí odkaz:
https://doaj.org/article/86b04fea61334ffe80f3605964adc1ba
Publikováno v:
Translational Neurodegeneration, Vol 12, Iss 1, Pp 1-17 (2023)
Abstract Multiple system atrophy (MSA) is a fatal progressive neurodegenerative disease. Biomarkers are urgently required for MSA to improve the diagnostic and prognostic accuracy in clinic and facilitate the development and monitoring of disease-mod
Externí odkaz:
https://doaj.org/article/314b801f1d4d46eaa1ba37824826c6e3
Autor:
Daji Chen, Linlin Wan, Zhao Chen, Xinrong Yuan, Mingjie Liu, Zhichao Tang, You Fu, Sudan Zhu, Xuewei Zhang, Rong Qiu, Beisha Tang, Hong Jiang
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2023)
AimThere is increasing evidence suggesting that vitamins may play important roles in the pathogenesis of multiple system atrophy (MSA). The purpose of this study was to detect the changes of serum vitamin levels and investigate their correlation with
Externí odkaz:
https://doaj.org/article/cd01f8215cd54c9fb744daea39b045cd
Autor:
Lang He, Shang Wang, Linliu Peng, Huifang Zhao, Shuai Li, Xiaobo Han, Jean de Dieu Habimana, Zhao Chen, Chunrong Wang, Yun Peng, Huirong Peng, Yue Xie, Lijing Lei, Qi Deng, Linlin Wan, Na Wan, Hongyu Yuan, Yiqing Gong, Guangdong Zou, Zhiyuan Li, Beisha Tang, Hong Jiang
Publikováno v:
Translational Psychiatry, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Spinocerebellar ataxia type 3/Machado–Joseph disease (SCA3/MJD) is a progressive autosomal dominant neurodegenerative disease caused by abnormal CAG repeats in the exon 10 of ATXN3. The accumulation of the mutant ataxin-3 proteins carrying
Externí odkaz:
https://doaj.org/article/9315911a81a34e1b9d350b4d37f326db
Autor:
Yun Peng, Linliu Peng, Zhao Chen, Huirong Peng, Puzhi Wang, Youming Zhang, Yangping Li, Chunrong Wang, Yuting Shi, Xuan Hou, Zhe Long, Hongyu Yuan, Na Wan, Linlin Wan, Keqin Xu, Lijing Lei, Shang Wang, Lang He, Yue Xie, Yiqing Gong, Qi Deng, Guangdong Zou, Zhichao Tang, Lu Shen, Kun Xia, Rong Qiu, Thomas Klockgether, Beisha Tang, Hong Jiang
Publikováno v:
Frontiers in Aging Neuroscience, Vol 14 (2022)
ObjectiveThe natural history of spinocerebellar ataxia type 3 (SCA3) has been reported in several populations and shows heterogeneity in progression rate and affecting factors. However, it remains unexplored in the population of Mainland China. This
Externí odkaz:
https://doaj.org/article/1e0d2b56ff784f9ab990e042df4caaca
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
Spinocerebellar ataxia type 3/Machado–Joseph disease (SCA3/MJD) is a progressive autosomal dominantly inherited cerebellar ataxia characterized by the aggregation of polyglutamine-expanded protein within neuronal nuclei in the brain, which can lead
Externí odkaz:
https://doaj.org/article/7b6464edd5ec46c48826bd9a0f9553bf
Autor:
Linlin Wan, Xin Zhou, Chunrong Wang, Zhao Chen, Huirong Peng, Xuan Hou, Yun Peng, Puzhi Wang, Tianjiao Li, Hongyu Yuan, Yuting Shi, Xiaocan Hou, Keqin Xu, Yue Xie, Lang He, Kun Xia, Beisha Tang, Hong Jiang
Publikováno v:
Frontiers in Neuroscience, Vol 14 (2020)
Externí odkaz:
https://doaj.org/article/5a862b64e28447e5b48598563e78bcf0
Publikováno v:
Lipids in Health and Disease, Vol 17, Iss 1, Pp 1-9 (2018)
Abstract Background Fragarianilgerrensis Schlecht. medicine compound (FN-MC) is a kind of Chinese herbs’ compound consisted of Fragarianilgerrensis Schlecht. and Centella asiatica (L.) Urban. The study was to investigate the hypolipidemia effect of
Externí odkaz:
https://doaj.org/article/df5d412b4bb24dcd830a2fe09183c97f