Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Li-ri Jin"'
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 6, Pp 911-923 (2020)
Abstract Objective Type I sialidosis (ST‐1) is a rare autosomal recessive inherited disorder. To date, there has been no study on ST‐1 patients in mainland China. Methods We reported in detail the cases of five Chinese ST‐1 patients from two ce
Externí odkaz:
https://doaj.org/article/7e8f2de99dc64047b1d2822492236af7
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 18, Iss 5, Pp 331-335 (2018)
Objective To summarize clinical seizures and electroencephalography (EEG) characteristics of patients with anti ? leucine ? rich glioma ? inactivated 1 (LGI1) antibody ? associated encephalitis. Methods Clinical manifestations, imaging and EEG charac
Externí odkaz:
https://doaj.org/article/0f6aeb91ffab4ca289e8e1bd42efe111
Publikováno v:
Chinese Medical Journal, Vol 131, Iss 24, Pp 2915-2920 (2018)
Background: Few studies have been published on new-onset geriatric epilepsy especially in older Chinese people. This study was to have a comprehensive understanding of new-onset geriatric epilepsy and find a more reasonable diagnosis and management o
Externí odkaz:
https://doaj.org/article/7546b3b6c59546c38133fb6001015681
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 13, Iss 7, Pp 641-645 (2013)
Externí odkaz:
https://doaj.org/article/b7d9962e6bb2409eb5e0182caf8d5a95
Publikováno v:
Chinese Medical Journal, Vol 129, Iss 2, Pp 248-249 (2016)
Externí odkaz:
https://doaj.org/article/7291b898c5904a7482d7d757c88d0c82
Publikováno v:
PLoS ONE, Vol 7, Iss 6, p e39152 (2012)
Growing evidence from rodent models of temporal lobe epilepsy (TLE) indicates that dysregulation of the mammalian target of rapamycin (mTOR) pathway is involved in seizures and epileptogenesis. However, the role of the mTOR pathway in the epileptogen
Externí odkaz:
https://doaj.org/article/6f57f10a2a894096bba131a860576b09
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 6, Pp 911-923 (2020)
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology
Objective Type I sialidosis (ST‐1) is a rare autosomal recessive inherited disorder. To date, there has been no study on ST‐1 patients in mainland China. Methods We reported in detail the cases of five Chinese ST‐1 patients from two centers, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c34368749b011a21b7a33b4c3a840df0
https://doaj.org/article/7e8f2de99dc64047b1d2822492236af7
https://doaj.org/article/7e8f2de99dc64047b1d2822492236af7
Autor:
Li Ling, Dong, Hong Zhi, Guan, Yan, Huang, Hong Lin, Hao, Jing Wen, Niu, Qing, Liu, Qiang, Lu, Dan, Xu, Jun Yi, Zhang, Li Xin, Zhou, Li Ri, Jin, Hai Tao, Ren, Yi Cheng, Zhu, Bin, Peng, Li Ying, Cui, Xiang Qin, Zhou
Publikováno v:
Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae. 41(3)
Objective To explore the clinical characteristics of autoimmune disease with dual seropositive antibodies of leucine-rich glioma inactivated 1(LGI1)and contactin-associated protein 2(Caspr2).Methods The clinical data of seven patients with dual serop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ab2c94752cd31695aa08417de7742bf1
https://pubmed.ncbi.nlm.nih.gov/31282328
https://pubmed.ncbi.nlm.nih.gov/31282328
Autor:
Qiang Lu, Ya-qing Zhang, Hui Liu, Rui-Juan Lv, Li-wen Wu, Jin-sheng He, Yuan-hui Fu, Li-ri Jin, Xiao-Qiu Shao
Publikováno v:
Epilepsy Research. 96:74-80
Recent in vitro and in vivo data show that acid-sensing ion channel 1a (ASIC1a) activation enhances neuronal excitability in the hippocampus and neocortex, indicating that ASIC1a might play a role in the generation and maintenance of epileptic seizur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc1cc66075c323e75cec5236f97829f2
https://doi.org/10.1016/j.eplepsyres.2011.05.002
https://doi.org/10.1016/j.eplepsyres.2011.05.002
Autor:
Rui-Juan Lv, Li-wen Wu, Xiao-Qiu Shao, Li-ri Jin, Qiang Lu, Hui Liu, Jin-sheng He, Yuan-hui Fu
Publikováno v:
Epilepsy & Behavior. 20:681-685
A recent study suggests that the P86L polymorphism (rs2986017) in the calcium homeostasis modulator 1 (CALHM1) gene interferes with calcium homeostasis and increases amyloid β (Aβ) levels. Moreover, in vitro and in vivo data show that both calcium
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86ca5df09bc235c44c014f2e8512bbd5
https://doi.org/10.1016/j.yebeh.2011.02.007
https://doi.org/10.1016/j.yebeh.2011.02.007