Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Ming‐Fan Hong"'
Publikováno v:
BMC Neurology, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Objective To analyze and explore the risk factors for neurological symptoms in patients with purely hepatic Wilson's disease (WD) at diagnosis. Methods This retrospective study was conducted at the First Affiliated Hospital of the Guangdong
Externí odkaz:
https://doaj.org/article/064595a35c364e33a91592b992ce24e8
Autor:
Wei‐Qin Ning, Chun‐Xiao Lyu, Sheng‐Peng Diao, Ye‐Qing Huang, Ai‐Qun Liu, Qing‐Yun Yu, Zhong‐Xing Peng, Ming‐Fan Hong, Zhi‐Hua Zhou
Publikováno v:
Brain and Behavior, Vol 13, Iss 6, Pp n/a-n/a (2023)
Abstract Background Morphological changes of retina in patients with Wilson's disease (WD) can be found by optical coherence tomography (OCT), and such changes had significant differences between neurological forms (NWD) and hepatic forms (HWD) of WD
Externí odkaz:
https://doaj.org/article/3b426a108dc141e498417ba542ae498f
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
BackgroundMitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) is one of the most common maternally inherited mitochondrial diseases which rarely affects elderly people.Case presentationWe reported the case of a 61-ye
Externí odkaz:
https://doaj.org/article/3d8e54e12c7e4c598794e2f9bcf26961
Autor:
Zhi-Hua Zhou, Yun-Fan Wu, Wei-Feng Wu, Ai-Qun Liu, Qing-Yun Yu, Zhong-Xing Peng, Ming-Fan Hong
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-4 (2020)
Abstract Background Bilateral medial medullary infarction (MMI) is uncommon and bilateral medial pons infarction (MPI) is even rarer. “Heart appearance” on magnetic resonance imaging (MRI) is a characteristic presentation of bilateral medial medu
Externí odkaz:
https://doaj.org/article/5259d88021584d0890bbf5aa5b590e98
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:
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:
Li Zhou, Di Chen, Xu-Ming Huang, Fei Long, Hua Cai, Wen-Xia Yao, Zhong-Cheng Chen, Zhi-Jian Liao, Zhe-Zhi Deng, Sha Tan, Yi-Long Shan, Wei Cai, Yu-Ge Wang, Ri-Hong Yang, Nan Jiang, Tao Peng, Ming-Fan Hong, Zheng-Qi Lu
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 11 (2017)
β-Amyloid protein (Aβ) is thought to cause neuronal loss in Alzheimer’s disease (AD). Aβ treatment promotes the re-activation of a mitotic cycle and induces rapid apoptotic death of neurons. However, the signaling pathways mediating cell-cycle a
Externí odkaz:
https://doaj.org/article/62066c4d7fc5412da5ab8827276a4947
Autor:
Si-Qi Wang, Yong-Qiang Zhan, Xuan Hu, Yu-Pei Zhuang, Hong-Qian Liu, Ming-Fan Hong, Hao-Jie Zhong
Publikováno v:
Digestive Diseases.
Introduction: Anemia is a common manifestation of chronic liver diseases. It is a predictor of severe disease, a high risk of complications, and poor outcomes in various liver diseases. However, it remains unclear whether anemia serves as a similar i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a3d7ce01ba5925944d758f95eb15cf9
https://doi.org/10.1159/000530473
https://doi.org/10.1159/000530473
Autor:
null Wei‐Qin Ning, null Chun‐Xiao Lyu, null Sheng‐Peng Diao, null Ye‐Qing Huang, null Ai‐Qun Liu, null Qing‐Yun Yu, null Zhong‐Xing Peng, null Ming‐Fan Hong, null Zhi‐Hua Zhou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f65602982dfcbefd721188d373a1b062
https://doi.org/10.1002/brb3.3014/v2/response1
https://doi.org/10.1002/brb3.3014/v2/response1
Autor:
Wei Qin Ning, Chun Xiao Lyu, Sheng-Peng Diao, Ye-Qing Huang, Ai-Qun Liu, Qing-Yun Yu, Ming-Fan Hong, Zhong-Xing Peng, ZhiHua Zhou
Background: Morphological changes of retina in patients with Wilson’s disease (WD) can be found by optical coherence tomography (OCT), and such changes have significant differences between neurological forms（NWD ) and hepatic forms (HWD) of WD. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d88617efce45e79fe38c9abcc4bb2ed
https://doi.org/10.21203/rs.3.rs-2225780/v1
https://doi.org/10.21203/rs.3.rs-2225780/v1