Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Gong-Qiang Wang"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract According to early research, the incidence of claustrum lesions in patients with neurological Wilson’s disease (WD) was inconsistent, ranging from 1.8 to 75% on magnetic resonance imaging (MRI). Our study aims to explore the incidence, cli
Externí odkaz:
https://doaj.org/article/b4d7a896591b45b9b83ca5be14f315f1
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Hereditary spastic paraplegias (HSP) are inherited neurodegenerative disorders characterized by progressive paraplegia and spasticity in the lower limbs. SPG48 represents a rare genotype characterized by mutations in AP5Z1, a gene playing a role in i
Externí odkaz:
https://doaj.org/article/8c98e010e5f7482380ac953387e77839
Autor:
Zhi‐Hua Zhou, Yun‐Fan Wu, Yan Yan, Ai‐Qun Liu, Qing‐Yun Yu, Zhong‐Xing Peng, Gong‐Qiang Wang, Ming‐Fan Hong
Publikováno v:
Brain and Behavior, Vol 11, Iss 6, Pp n/a-n/a (2021)
Abstract Background Wilson's disease (WD) is one of the few hereditary diseases that can be successfully treated with medicines. We conduct this survey research to assess treatment persistence among patients with WD and try to identify what factors a
Externí odkaz:
https://doaj.org/article/ba2569bb57d64f5eb52317d81b9660e6
Autor:
Zhi-Hua Zhou, Yun-Fan Wu, Jin Cao, Ji-Yuan Hu, Yong-Zhu Han, Ming-Fan Hong, Gong-Qiang Wang, Shu-Hu Liu, Xue-Min Wang
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-5 (2019)
Abstract Background Wilson’s disease (WD) is an autosomal recessive disease of impaired copper metabolism. Previous study demonstrated that WD with corpus callosum abnormalities (WD-CCA) was limited to the posterior part (splenium). This study aime
Externí odkaz:
https://doaj.org/article/89955aa2373c4ba294cf642708b184ab
Autor:
Yong-zhu Han, Gong-qiang Wang, Jin Cao, Yun-Fan Wu, Mingfan Hong, Xue-min Wang, Shu-Hu Liu, Ji-yuan Hu, Zhi-Hua Zhou
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-5 (2019)
BMC Neurology
BMC Neurology
Background Wilson’s disease (WD) is an autosomal recessive disease of impaired copper metabolism. Previous study demonstrated that WD with corpus callosum abnormalities (WD-CCA) was limited to the posterior part (splenium). This study aimed to comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cc04d4ff153bee92e6df693d3c1f5a5
http://link.springer.com/article/10.1186/s12883-019-1313-7
http://link.springer.com/article/10.1186/s12883-019-1313-7
Publikováno v:
Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine. 33(11)
To explore the correlation between Chinese medical syndrome types of Wilson's disease (WD) and clinical materials as well as physical and chemical indices.Totally 116 WD patients were typed by Chinese medical syndrome. The correlation between Chinese
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::56418a3e75e0fad163a5831ed0029dce
https://pubmed.ncbi.nlm.nih.gov/24483109
https://pubmed.ncbi.nlm.nih.gov/24483109
Publikováno v:
Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine. 33(3)
To explore the correlation between neuropsychological features and Chinese medical syndrome types in Wilson's disease (WD) patients, thus providing evidence for early intervention by syndrome typing.Totally 96 WD patients were assigned to Gan-Dan dam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2d6fd3d1f6041dc0d58114e6fdeb19f0
https://pubmed.ncbi.nlm.nih.gov/23713242
https://pubmed.ncbi.nlm.nih.gov/23713242
Autor:
Ji-yuan, Hu, Gong-qiang, Wang, Nan, Cheng, Xun, Wang, Mingfan, Hong, Yongzhu, Han, Renmin, Yang
Publikováno v:
Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine. 24(9)
To observe the clinical manifestation of 155 patients with hepatolenticular degeneration (HLD) complicated with epilepsy and the therapeutic effect of integrative Chinese and Western medicine treatment on them.Clinical manifestation of patients and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c12b94f0c7279ec10e6a152f1fa2dd6e
https://pubmed.ncbi.nlm.nih.gov/15495822
https://pubmed.ncbi.nlm.nih.gov/15495822
Autor:
Gong-Qiang Wang, Yu-Xin Fan, Wen-Bin Hu, Shuang-Wu Ju, Zhi Zhang, Ming-Shan Ren, Ren-Min Yang
AIM:To investigate the copper-chelating therapeutic effect in Wilson disease (WD) with different clinical phenotypes and polymorphisms of ATP7B gene.METHODS:One hundred and twenty-two WD patients with different clinicalphenotypes were given DMPS intr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41fcfd505cda3ab8726d6026d3694d39
https://europepmc.org/articles/PMC4761557/
https://europepmc.org/articles/PMC4761557/
