Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Xuen Yu"'
Autor:
Kexin Jiao, Jihong Dong, Sushan Luo, Liqiang Yu, Qing Ke, Zhiqiang Wang, Xinghua Luan, Xiaojie Zhang, Junhong Guo, Yan Chen, Xihua Li, Song Tan, Fangyuan Qian, Jianming Jiang, Xuen Yu, Dongyue Yue, Changxia Liu, Lijun Luo, Jianping Li, Yanzhou Qu, Lan Chen, Jianglong Tu, Chong Sun, Chong Yan, Jie Song, Jianying Xi, Jie Lin, Jiahong Lu, Chongbo Zhao, Wenhua Zhu, Qi Fang
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
IntroductionThe lack of knowledge regarding the differences between Chinese and other ethnicities in the early manifestation of late-onset Pompe disease (LOPD) prohibits the development of an effective screening strategy. We conducted a multicenter s
Externí odkaz:
https://doaj.org/article/83bc4ce35aba41e78a0aec065305079a
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:
Juanjuan Zhang, Dandan Xie, Yanfeng Zou, Xuen Yu, Yang Ji, Chengyou Wang, Xinyi Lv, Nong Zhou, Xiao Jiang, Kai Wang, Yanghua Tian
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Background: Nitrous oxide (N2O), commonly known as laughing gas, is inhaled recreationally because it produces the feelings of euphoria and freedom from pain. The risk of neurological dysfunction secondary to N2O abuse and its clinical diagnosis are,
Externí odkaz:
https://doaj.org/article/5e0276021cee4631a4cb113b85e91a87
Autor:
Xiaohu Li, Zhiqiang Feng, Wei Tang, Xuen Yu, Yinfeng Qian, Bin Liu, Xiaoshu Li, Renmin Yang, Yongqiang Yu
Publikováno v:
Frontiers in Physiology, Vol 9 (2018)
Background: Wilson’s disease (WD) is an inborn copper metabolism disease. Sex differences in clinical features of WD patients have been reported; however, the effect of sex on brain MRI is still unclear, especially for Chinese WD patients. Therefor
Externí odkaz:
https://doaj.org/article/87f28ba886f848d6beb20a0876831f45
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0125100 (2015)
It is well known that patients with Wilson's disease (WD) suffer copper metabolism disorder. However, recent studies point to an additional iron metabolism disorder in WD patients. The purpose of our study was to examine susceptibility-weighted imagi
Externí odkaz:
https://doaj.org/article/feefaea630ba4a7380f93a37c4befed4
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
Autor:
Chong Yan, Jie Lin, Jianping Li, Yan Chen, Jianying Xi, Xihua Li, Qing Ke, Fangyuan Qian, Wenhua Zhu, Zhiqiang Wang, Chong Sun, Jie Song, Changxia Liu, Yanzhou Qu, Jihong Dong, Jianglong Tu, Junhong Guo, Xinghua Luan, Jianming Jiang, Qi Fang, Chongbo Zhao, Lan Chen, Xiaojie Zhang, Liqiang Yu, Kexin Jiao, Lijun Luo, Dongyue Yue, Jiahong Lu, Song Tan, Sushan Luo, Xuen Yu
Backgroud: Pompe disease is a rare metabolic disorder with available enzymatic replacement therapy. Contrasting with the classic infantile form, the others subtypes have a heterogeneous presentation that makes an early and accurate diagnosis difficul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a91bc845e7100772e6987c532a93a6d
https://doi.org/10.21203/rs.3.rs-1104428/v1
https://doi.org/10.21203/rs.3.rs-1104428/v1
Autor:
Liangliang, Zhang, Long, Zhang, Na, Nian, Xuen, Yu, Yongguang, Shi, Yan, Yan, Dandan, Sun, Nan, Cheng, Xun, Wang, Renmin, Yang
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 33(4)
To analyze a case of cerebrotendinous xanthomatosis (CTX) with mental retardation as the initial neurological symptom.Medical imaging, histopathological assay and genetic testing were carried out to analyze the patient.Neurological manifestations of
Autor:
Nan, Cheng, Xun, Wang, Xuen, Yu, Zhihua, Zhou, Mingwei, Gao, Rao, Rao, Jiyuan, Hu, Renmin, Yang, Yongzhu, Han
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 30(3)
To study the clinical and genetic characteristics of twins and siblings affected with Wilson's disease (WD).Clinical data and blood samples were collected from the subjects after informed consent was obtained. Genomic DNA was extracted and potential
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0125100 (2015)
PLoS ONE
PLoS ONE
Purpose It is well known that patients with Wilson’s disease (WD) suffer copper metabolism disorder. However, recent studies point to an additional iron metabolism disorder in WD patients. The purpose of our study was to examine susceptibility-weig