Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Ru‐Wei Ou"'
Autor:
Yang‐Fan Cheng, Kun‐Cheng Liu, Tian‐Mi Yang, Yi Xiao, Qi‐Rui Jiang, Jing‐Xuan Huang, Sirui Zhang, Qian‐Qian Wei, Ru‐Wei Ou, Chun‐Yu Li, Xiao‐Jing Gu, Jean‐Marc Burgunder, Hui‐Fang Shang
Publikováno v:
Brain and Behavior, Vol 13, Iss 11, Pp n/a-n/a (2023)
Abstract Background and aim Huntington's disease (HD) is an autosomal dominant inherited neurodegenerative disorder caused by CAG repeats expansion. Cognitive decline contributes to the loss of daily activity in manifest HD. We aimed to examine the c
Externí odkaz:
https://doaj.org/article/8b1ab19aa9d9438da3df0e48b49ceb15
Autor:
Qian-Qian Wei, Yan-Bing Hou, Ling-Yu Zhang, Ru-Wei Ou, Bei Cao, Yong-Ping Chen, Hui-Fang Shang
Publikováno v:
Neural Regeneration Research, Vol 17, Iss 4, Pp 875-880 (2022)
The neutrophil-to-lymphocyte ratio (NLR) is considered a robust prognostic biomarker for predicting patient survival outcomes in many diseases. However, it remains unclear whether it can be used as a biomarker for amyotrophic lateral sclerosis (ALS).
Externí odkaz:
https://doaj.org/article/46fb561e3d334e3a8f3c47c0c0aaeb45
Autor:
Ling Yu Zhang, Bei Cao, Qian-Qian Wei, Ru Wei Ou, Bi Zhao, Jing Yang, Ying Wu, Hui Fang Shang
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-9 (2021)
Abstract Background Camptocormia is common in patients with multiple system atrophy (MSA). The current study was aimed at assessing the frequency of camptocormia and its related factors in MSA patients with different disease durations. Also, the impa
Externí odkaz:
https://doaj.org/article/ba55148dcb4d4899abd90d71e4485ad2
Autor:
Jun-Yu Lin, Ling-Yu Zhang, Bei Cao, Qian-Qian Wei, Ru-Wei Ou, Yan-Bing Hou, Kun-Cheng Liu, Xin-Ran Xu, Zheng Jiang, Xiao-Jing Gu, Jiao Liu, Hui-Fang Shang, Li-Shao Guo
Publikováno v:
Chinese Medical Journal, Vol 134, Iss 6, Pp 690-698 (2021)
Abstract. Background:. Sleep disorders are common but under-researched symptoms in patients with multiple system atrophy (MSA). We investigated the frequency and factors associated with sleep-related symptoms in patients with MSA and the impact of sl
Externí odkaz:
https://doaj.org/article/a1205226cb6a4162b4651ea66ee05f1c
Publikováno v:
BMC Medicine, Vol 19, Iss 1, Pp 1-11 (2021)
Abstract Background Epidemiological and clinical studies have suggested comorbidity between amyotrophic lateral sclerosis (ALS) and autoimmune disorders. However, little is known about their shared genetic architecture. Methods To examine the relatio
Externí odkaz:
https://doaj.org/article/63c80494230e442e923e9840a19f08e4
Autor:
Xue-Ping Chen, Qian-Qian Wei, Ru-Wei Ou, Yan-Bing Hou, Ling-Yu Zhang, Xiao-Qin Yuan, Yun-Qian Yao, De-Sheng Jia, Qian Zhang, Wei-Xue Li, Hui-Fang Shang
Publikováno v:
Neural Regeneration Research, Vol 16, Iss 3, Pp 591-595 (2021)
Creatine kinase is a muscle enzyme that has been reported at various levels in different studies involving patients with amyotrophic lateral sclerosis. In the present retrospective case-control study, we included 582 patients with amyotrophic lateral
Externí odkaz:
https://doaj.org/article/bfa3630d91c54ff4838da6e04130b2d7
Autor:
Yong-Ping Chen, Ru-Wei Ou, Xiao-Jing Gu, Ling-Yu Zhang, Bei Cao, Yan-Bing Hou, Kun-Cheng Liu, Jun-Yu Lin, Qian-Qian Wei, Bi Zhao, Ying Wu, Hui-Fang Shang
Publikováno v:
Translational Neurodegeneration, Vol 10, Iss 1, Pp 1-3 (2021)
Externí odkaz:
https://doaj.org/article/4ba4889ced6b4dc2bbcac00f989600a1
Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11
Autor:
Xueping Chen, Jiao Liu, Qian-Qian Wei, Ru Wei Ou, Bei Cao, Xiaoqin Yuan, Yanbing Hou, Lingyu Zhang, Huifang Shang
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-8 (2020)
Abstract Background Spastic paraplegia type 11 (SPG11) mutations are the most frequent cause of autosomal recessive hereditary spastic paraplegia (ARHSP). We are aiming to identify the causative mutations in SPG11 among families referred to our cente
Externí odkaz:
https://doaj.org/article/293bcac9329643879d83bbf9a1d98dec
Publikováno v:
Frontiers in Aging Neuroscience, Vol 13 (2021)
Background: Few studies have focused on the cold hand sign (CHS), a red flag symptom, in multiple system atrophy (MSA).Objective: This study aimed to investigate the frequency and correlative factors of CHS in patients with MSA and the impact of its
Externí odkaz:
https://doaj.org/article/e7d6534e50134bf2bb46d71c30510857
Autor:
Wei-Ming Su, Xiao-Jing Gu, Yan-Bing Hou, Ling-Yu Zhang, Bei Cao, Ru-Wei Ou, Ying Wu, Xue-Ping Chen, Wei Song, Bi Zhao, Hui-Fang Shang, Yong-Ping Chen
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Background: The association between inflammation and neurodegeneration has long been observed in parkinson’s disease (PD) and multiple system atrophy (MSA). Previous genome-wide association studies (GWAS) and meta-analyses have identified several r
Externí odkaz:
https://doaj.org/article/4769c9cc41c445d7bc226fded8a1cedf