Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Yong-zhu Han"'
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
ObjectivesWilson’s disease is an autosomal recessive disorder related to copper metabolism which mostly patients occurs in adolescents, fertility has become a problem that WD needs to face.MethodsA 21 years retrospective follow up study was conduct
Externí odkaz:
https://doaj.org/article/cc8b57cb783444a090eba4454c53cf4f
Autor:
Shi-jing Wang, Hao Geng, Si-rui Cheng, Chen-chen Xu, Rui-qi Zhang, Yu Wang, Tong Wu, Bo Li, Tao Wang, Yong-sheng Han, Zeng-hui Ding, Yi-ning Sun, Xun Wang, Yong-zhu Han, Nan Cheng
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
ObjectivesCranial magnetic resonance imaging (MRI) could be a crucial tool for the assessment for neurological symptoms in patients with Wilson’s disease (WD). Diffusion-weighted imaging (DWI) hyperintensity reflects the acute brain injuries, which
Externí odkaz:
https://doaj.org/article/bf165d94938e4b1aab0695acb137fd76
Autor:
Lin Chen, Yin Xu, Ming-juan Fang, Yong-guang Shi, Jie Zhang, Liang-liang Zhang, Yu Wang, Yong-zhu Han, Ji-yuan Hu, Ren-min Yang, Xu-en Yu
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
Gerstmann-Sträussler-Scheinker syndrome (GSS) is a rare genetic prion disease caused by a mutation in the prion protein (PRNP) gene. It is typically characterized by progressive cerebellar ataxia and slowly progressive dementia. We present a case st
Externí odkaz:
https://doaj.org/article/1555b7b6dc994b57a9d660be871e0a3e
Publikováno v:
BMC Pregnancy and Childbirth, Vol 19, Iss 1, Pp 1-5 (2019)
Abstract Introduction Pregnancy management in women with Wilson disease (WD) remains an important clinical problem. This research was conducted to investigate how to avoid worsening of WD symptoms during pregnancy and increase pregnancy success in wo
Externí odkaz:
https://doaj.org/article/aa730f061d42463481da5da165f3a7c3
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:
Neurological Sciences. 40:1059-1066
Wilson’s disease (WD) is an autosomal recessive inherited disorder of copper (Cu) metabolism. Inflammation is a self-defensive reaction aimed at eliminating or neutralizing injurious stimuli, and restoring tissue integrity. Copper deposition may le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b9147ee3951af8b881d45490818e7bb
https://doi.org/10.1007/s10072-018-3680-z
https://doi.org/10.1007/s10072-018-3680-z
Autor:
Yong-zhu Han, Yongsheng Han, Yun Wu, Hongyi Yang, Chenchen Xu, Guangda Li, Shan Shu, Nan Cheng, Jianjian Dong, Rao Rao, Kai Zhong
Publikováno v:
Frontiers in Behavioral Neuroscience
Frontiers in Behavioral Neuroscience, Vol 14 (2020)
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::362bbff7ffd4ed3bf017299785787c12
http://europepmc.org/articles/PMC7189732
http://europepmc.org/articles/PMC7189732
Publikováno v:
Neurological Sciences. 38:547-552
Parkinson's disease (PD) is an insidious onset neurodegenerative disease affecting approximately 1% of the population over the age of 65. So far available therapies for PD have only aimed at improving or alleviating symptoms, but not at slowing, prev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a97076b91d20ab57bd962ce6406e5f8
https://doi.org/10.1007/s10072-016-2808-2
https://doi.org/10.1007/s10072-016-2808-2
Publikováno v:
Medicine
Rationale: Both Wilson disease (WD) and Oculocutaneous Albinism (OCA) are rare autosomal recessive disorders that are caused by mutations on chromosome 13 and chromosome 11, respectively. Here, we report on a patient with coexisting WD and OCA, initi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64afc2dec698b99fdd62d0660951fccd
http://europepmc.org/articles/PMC6320091
http://europepmc.org/articles/PMC6320091