Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Heqian Du"'
Publikováno v:
BMC Neurology, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background Stress hyperglycemia is a relatively transient increase in blood glucose in response to inflammation of the body and neurohormonal disorders. It is still debated whether stress hyperglycemia ratio (SHR) in the acute phase, a new i
Externí odkaz:
https://doaj.org/article/1fd1d85986e341b3a5f515cbabaa69e3
Publikováno v:
Frontiers in Neurology, Vol 14 (2024)
BackgroundCerebral amyloid angiopathy (CAA), a cerebral small vessel disease affecting leptomeningeal and cortical small blood vessels, is a common cause of spontaneous lobar intracerebral hemorrhage and cognitive impairment, particularly in elderly
Externí odkaz:
https://doaj.org/article/2fb10cadd13c49a98005e79946ce7dab
Publikováno v:
PLoS ONE, Vol 13, Iss 3, p e0194501 (2018)
To investigate the efficacy and tolerability of duloxetine during short-term treatment in adults with generalized anxiety disorder (GAD).We conducted a comprehensive literature review of the PubMed, Embase, Cochrane Central Register of Controlled Tri
Externí odkaz:
https://doaj.org/article/31bf5179dcb44d6ab5d51074b7c92315
Autor:
Heqian Du1, Xinyuan Li1, Hongmei Meng1, Ziwen Lu1, Lijun Zhu2, Shaokuan Fang1 fang20063536@sina.com
Publikováno v:
Neurology Asia. Dec2017, Vol. 22 Issue 4, p353-356. 4p.
Autor:
Li Xinyuan, Hongliang Zhang, Jing Liu, Shaokuan Fang, Chenglin Wang, Heqian Du, Li Cui, Lijun Zhu
Publikováno v:
NeuroQuantology. 16
Hereditary coproporphyria (HCP) is a form of porphyria arising from a deficiency of the enzyme, coproporphyrinogen oxidase, which results in the accumulation of coproporphyrin in the heme biosynthetic pathway. In the current study, we report a case o
Publikováno v:
PLoS ONE
PLoS ONE, Vol 13, Iss 3, p e0194501 (2018)
PLoS ONE, Vol 13, Iss 3, p e0194501 (2018)
Objective To investigate the efficacy and tolerability of duloxetine during short-term treatment in adults with generalized anxiety disorder (GAD). Methods We conducted a comprehensive literature review of the PubMed, Embase, Cochrane Central Registe
Autor:
Xinyuan, Li, Weihong, Lin, Lijun, Zhu, Yonghong, Wang, Shan, Liu, Jing, Liu, Heqian, Du, Shaokuan, Fang
Publikováno v:
Neuro endocrinology letters. 38(7)
Hereditary thrombophilia is a blood coagulation disorder that increases the risk of venous thromboembolism, due to several genetic risk factors. Factor V Leiden(FVL) is the most common contributing factor to thrombophilia in the Caucasian population
Autor:
Chenglin Wang, Heqian Du, Lijun Zhu, Li Cui, Jing Liu, Chunkui Zhou, Shaokuan Fang, Xinyuan Li
Publikováno v:
Medicine. 97:e12148
Rationale Spinocerebellar ataxia (SCA), a genetically inherited heterogeneous disorder, is characterized by gait ataxia, dysarthria, parkinsonism, choreic movements, dystonia, epilepsy, cognitive and psychiatric symptoms. Spinocerebellar ataxia-42 (S
Autor:
Xinyuan Li, Chunkui Zhou, Li Cui, Lijun Zhu, Heqian Du, Jing Liu, Chenglin Wang, Shaokuan Fang, Li, Xinyuan, Zhou, Chunkui, Cui, Li, Zhu, Lijun, Du, Heqian, Liu, Jing, Wang, Chenglin, Fang, Shaokuan
Publikováno v:
Medicine; Sep2018, Vol. 97 Issue 36, p1-5, 5p
Autor:
Chenglin Wang1, Jiguo Gao1, Beilin Zhang1, Rensheng Zhang1, Chao Wang1, Xinyuan Li1, Heqian Du1, Chunkui Zhou1 fang20063536@sina.com, Shaokuan Fang1 zhouchunkui@163.com
Publikováno v:
Neurology Asia. Sep2019, Vol. 24 Issue 3, p215-227. 13p.