Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Yongzhu Han"'
Autor:
Gongqiang Wang, Ping Jin, Xinfeng Ma, Xia Hong, Long Zhang, Kang Lin, Xiao Wen, Xue Bai, Yongzhu Han
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
BackgroundCognitive and motor dual-tasks play important roles in daily life. Dual-task interference impacting gait performance has been observed not only in healthy subjects but also in subjects with neurological disorders. Approximately 44–75% of
Externí odkaz:
https://doaj.org/article/9947393b87744ddda58f36b62bab16c8
Autor:
Lin Chen, Yongguang Shi, Nan Wang, Zhuoqi Lou, Liya Pan, Xiaolan Xu, Chensi Wu, Yongzhu Han, Renmin Yang, Wenbin Hu, Bing Ruan
Publikováno v:
International Journal of Clinical Practice, Vol 2023 (2023)
Background and Aim. Significantly reduced serum ceruloplasmin (Cp) is the most important clue in the diagnosis of Wilson’s disease (WD) and is well known to clinicians. The false increase in Cp in some WD patients, which overlaps with that in non-W
Externí odkaz:
https://doaj.org/article/a988056a310d4218b7e44ea8de340032
Autor:
Lin Chen, Nan Wang, Wenbin Hu, Xuen Yu, Renming Yang, Yongzhu Han, Yan Yan, Na Nian, Congbo Sha
Publikováno v:
BMC Musculoskeletal Disorders, Vol 22, Iss 1, Pp 1-6 (2021)
Abstract Background Polyglucosan body myopathy 1 (PGBM1) is a type of glycogen storage disease that can cause skeletal muscle myopathy and cardiomyopathy with or without immunodeficiency due to a pathogenic mutation in the RBCK1 gene. PGBM1 has been
Externí odkaz:
https://doaj.org/article/2584d1ab09774b60a5a8c7f62c3b8eb5
Autor:
Jianjian Dong, Xun Wang, Chenchen Xu, Manli Gao, Shijing Wang, Jin Zhang, Haiyang Tong, Lulu Wang, Yongzhu Han, Nan Cheng, Yongsheng Han
Publikováno v:
Cell Death and Disease, Vol 12, Iss 1, Pp 1-12 (2021)
Abstract Wilson’s disease (WD) is an inherited disorder characterized by excessive accumulation of copper in the body, particularly in the liver and brain. In the central nervous system (CNS), extracellular copper accumulation triggers pathological
Externí odkaz:
https://doaj.org/article/37791c40319448c3a33940590178ea74
Autor:
Hao Geng, Shijing Wang, Yan Jin, Nan Cheng, Bin Song, Shan Shu, Bo Li, Yongsheng Han, Yongzhu Han, Lishen Gao, Zenghui Ding, Yang Xu, Xun Wang, Zuchang Ma, Yining Sun
Publikováno v:
Frontiers in Nutrition, Vol 8 (2021)
Background: Abnormal nutritional status is frequently seen in patients with chronic diseases. To date, no study has investigated the detailed characteristics of abnormal nutritional status among Wilson's disease (WD) patients in the Chinese cohort. T
Externí odkaz:
https://doaj.org/article/d97bc1467962410dbe0a877be4d294ef
Autor:
Jianjian Dong, Xiaoming Zhang, Shijing Wang, Chenchen Xu, Manli Gao, Songyang Liu, Xiaoxiao Li, Nan Cheng, Yongsheng Han, Xun Wang, Yongzhu Han
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2021)
Studies have indicated that oxidative stress plays a crucial role in the development of Parkinson’s disease (PD) and other neurodegenerative conditions. Research has also revealed that nuclear factor erythroid 2-related factor 2 (Nrf2) triggers the
Externí odkaz:
https://doaj.org/article/0aeb41af0c9243cb8ec0e3d4983587f0
Autor:
Yongsheng Han, Jianjian Dong, Chenchen Xu, Rao Rao, Shan Shu, Guangda Li, Nan Cheng, Yun Wu, Hongyi Yang, Yongzhu Han, Kai Zhong
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 14 (2020)
In the current study, we used 9.4-tesla magnetic resonance imaging (9.4T MRI) and inductively coupled plasma mass spectrometry (ICP-MS) to investigate the distribution of copper in the brain samples of a murine model of Wilson’s disease (WD) follow
Externí odkaz:
https://doaj.org/article/89f6fb5deea144cbafc5fd0afc32ea95
Publikováno v:
Iranian Journal of Public Health.
Background: Hepatolenticular degeneration (HLD) is an inherited disorder caused by the mutation in the adenosine triphosphatase copper transporting β gene (ATP7B). W aimed to explore the genetic changes in HLD using bioinformatics analysis. Methods:
Autor:
Lin Chen, Yongguang Shi, Nan Wang, Zhuoqi Lou, Chensi Wu, Liya Pan, Xiaolan Xu, Renmin Yang, Yongzhu Han, Wenbin Hu, Bing Ruan
Background: Significantly reduced serum ceruloplasmin (Cp) is the most important clue in the diagnosis of Wilson disease (WD) and is well known to clinicians. The false increase of Cp in some WD patients decrease the diagnostic accuracy. The aims of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d88637653e1a7243e3a5b3aca45d0ed
https://doi.org/10.21203/rs.3.rs-1081495/v2
https://doi.org/10.21203/rs.3.rs-1081495/v2
Autor:
Congbo Sha, Xuen Yu, Na Nian, Lin Chen, Nan Wang, Renming Yang, Yan Yan, Yongzhu Han, Wenbin Hu
Publikováno v:
BMC Musculoskeletal Disorders, Vol 22, Iss 1, Pp 1-6 (2021)
BMC Musculoskeletal Disorders
BMC Musculoskeletal Disorders
Background Polyglucosan body myopathy 1 (PGBM1) is a type of glycogen storage disease that can cause skeletal muscle myopathy and cardiomyopathy with or without immunodeficiency due to a pathogenic mutation in the RBCK1 gene. PGBM1 has been reported