Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Jun-yi SHEN"'
Publikováno v:
The Astrophysical Journal, Vol 951, Iss 1, p 3 (2023)
Magnetars are believed to be neutron stars (NSs) with strong magnetic fields. X-ray flares and fast radio bursts (FRBs) have been observed from the magnetar (soft gamma-ray repeater, SGR J1935+2154). We propose that the phase transition of the NS can
Externí odkaz:
https://doaj.org/article/b3fdea1381524f07b7f0c3dddf1f5151
Autor:
Wo-tu TIAN, Xiao-jun HUANG, Gui-ling LIANG, Chen-xi ZHU, Ying SHEN, Yu FANG, Mu-han CHEN, Jun-yi SHEN, Sheng-di CHEN, Li CAO
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 17, Iss 8, Pp 590-596 (2017)
Background Paroxysmal kinesigenic dyskinesia (PKD) is a rare involuntary movement disorder characterized by transient and recurrent dystonic or choreoathetoid attacks triggered by sudden voluntary movements. Since 2011, progress in genetics and patho
Externí odkaz:
https://doaj.org/article/da45eee8b6ee418e90f222543e8d70c3
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 17, Iss 7, Pp 534-540 (2017)
Objective To report 4 cases of fatty acid hydroxylase - associated neurodegeneration (FAHN) and to summarize the clinical and genetic characteristics of FAHN by literatures review. Methods Four cases of FAHN patients' clinical and family data were co
Externí odkaz:
https://doaj.org/article/00cbffadf6c14b3692a160177b62e05a
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 17, Iss 7, Pp 507-512 (2017)
Background Paroxysmal kinesigenic dyskinesia (PKD) is a disorder characterized by recurrent and brief dystonic or choreoathetoid attacks that are induced by sudden voluntary movement with highly clinical and genetic heterogeneity. We aimed to investi
Externí odkaz:
https://doaj.org/article/124cd1cb4f0e4298b3ae23a676ec7d42
Autor:
Wo-Tu Tian, Xiao-Jun Huang, Xiao-Li Liu, Jun-Yi Shen, Gui-Ling Liang, Chen-Xi Zhu, Wei-Guo Tang, Sheng-Di Chen, Yan-Yan Song, Li Cao
Publikováno v:
Chinese Medical Journal, Vol 130, Iss 17, Pp 2088-2094 (2017)
Background: Paroxysmal kinesigenic dyskinesia (PKD) is a rare movement disorder characterized by recurrent dystonic or choreoathetoid attacks triggered by sudden voluntary movements. Under the condition of psychological burden, some patients' attacks
Externí odkaz:
https://doaj.org/article/3950c7f7afe447eb9488180b6ac18287
Autor:
Wo-Tu Tian, Jun-Yi Shen, Xiao-Li Liu, Tian Wang, Xing-Hua Luan, Hai-Yan Zhou, Sheng-Di Chen, Xiao-Jun Huang, Li Cao
Publikováno v:
Chinese Medical Journal, Vol 129, Iss 22, Pp 2759-2761 (2016)
Externí odkaz:
https://doaj.org/article/b56d6e119d124d148752a0d25aabdc7d
Autor:
Ya-Chao He, Pei Huang, Qiong-Qiong Li, Qian Sun, Dun-Hui Li, Tian Wang, Jun-Yi Shen, Juan-Juan Du, Shi-Shuang Cui, Chao Gao, Rao Fu, Sheng-Di Chen
Publikováno v:
Parkinson's Disease, Vol 2017 (2017)
Background. HTRA2 has already been nominated as PARK13 which may cause Parkinson’s disease, though there are still discrepancies among these results. Recently, Gulsuner et al.’s study found that HTRA2 p.G399S is responsible for hereditary essenti
Externí odkaz:
https://doaj.org/article/b4fd1f310eac40a49820c2c81fcb837a
Publikováno v:
Phytomedicine : international journal of phytotherapy and phytopharmacology. 94
Ethnopharmacological relevance Uvangoletin is a dihydrochalcone extracted from the traditional Chinese medicinal plant Sarcandra glabra. Previous research has showed that uvangoletin could induce leukemia cell death. However, the anticancer effect of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d59e09438e93be56adf3eb0b60cfc5f6
https://pubmed.ncbi.nlm.nih.gov/34736000
https://pubmed.ncbi.nlm.nih.gov/34736000
Clinical correlates of decreased plasma coenzyme Q10 levels in patients with multiple system atrophy
Autor:
Tian Wang, Juan-Juan Du, Chao Gao, Shi-Shuang Cui, Sheng-Di Chen, Ya-Chao He, Pei Huang, Jun-Yi Shen, Yu-Yan Tan, Rao Fu, Yi-Qi Lin
Publikováno v:
Parkinsonism & Related Disorders. 57:58-62
Introduction Multiple system atrophy (MSA) is a progressive neurodegenerative disease. Recent studies revealed decreased coenzyme Q10 (COQ10) levels in the cerebellum and blood samples of MSA patients. But few studies focused on the associations of C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eabcc9fa6ca76030946e113e680bc1ab
https://doi.org/10.1016/j.parkreldis.2018.07.017
https://doi.org/10.1016/j.parkreldis.2018.07.017
Autor:
Xiao-Li Liu, Xiao-Rong Liu, Yang-Qi Xu, Hui-Dong Tang, Xiao-Jun Huang, Xiao-Meng Yin, Xia-Nan Guo, Qing Liu, Sheng Zeng, Mei Zhang, Wo-Tu Tian, Sheng-Di Chen, Li Cao, Xiao Mao, Jun-Yi Shen, Beisha Tang, Wei-Guo Tang
Publikováno v:
Movement Disorders. 33:459-467
Background Paroxysmal kinesigenic dyskinesia is the most common type of paroxysmal dyskinesia. Approximately half of the cases of paroxysmal kinesigenic dyskinesia worldwide are attributable to proline-rich transmembrane protein 2 mutations. Objectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9660f864ebf9825687e452cb78ee90e3
https://doi.org/10.1002/mds.27274
https://doi.org/10.1002/mds.27274