Zobrazeno 1 - 10
of 44
pro vyhledávání: '"LIAO Hong-mei"'
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 23, Iss 03, Pp 196-204 (2023)
Objective To analyze and summarize the clinical and genetic characteristics of potassium channel gene variation in infant epileptic encephalopathy (EE). Methods and Results A total of 11 infants with EE associated with potassium channel gene variatio
Externí odkaz:
https://doaj.org/article/d55b54a315ac48c69e9a54dc001147a0
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 21, Iss 04, Pp 304-309 (2021)
Objective To study the clinical characteristics, diagnosis, treatment and prognosis of a patient with childhood⁃onset rapid⁃onset dystonia Parkinsonism (RDP) caused by ATP1A3 gene mutation, and review the related literature. Methods The patient w
Externí odkaz:
https://doaj.org/article/096ebc74322a42a2a1b62b832873b803
Autor:
Wang, Yi, Yin, Li, Du, Yao-Yao, Liao, Hong-Mei, Li, Juan, Yao, Wen, Yuan, Xiao-Qiong, Guo, Qing-Chun, Deng, Tao-Ran, Guo, Na, Zhang, Min, Zeng, Qiang, Liu, Chong, Li, Yu-Feng
Publikováno v:
In Environmental Toxicology and Pharmacology June 2024 108
Autor:
Wang, Yi, Du, Yao-Yao, Yao, Wen, Deng, Tao-Ran, Guo, Na, Yin, Li, Yuan, Xiao-Qiong, Guo, Qing-Chun, Li, Juan, Liao, Hong-Mei, Qin, Dan-Yu, Li, Yu-Feng
Publikováno v:
In Ecotoxicology and Environmental Safety 15 November 2023 267
Akademický článek
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Autor:
Pan, Wen-Juan, Xiong, Can, Wu, Qiu-Ping, Liu, Jin-Xia, Liao, Hong-Mei, Chen, Wei, Liu, Yong-Sheng, Zheng, Lei
Publikováno v:
In Chemosphere November 2013 93(10):2585-2592
Akademický článek
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Autor:
Gong, Jiao-E., Liao, Hong-Mei, Long, Hong-Yu, Li, Xiang-Min, Long, Li-Li, Zhou, Luo, Gu, Wen-Ping, Lu, Shao-Hua, Qu, Qiang, Yang, Li-Min, Xiao, Bo, Qu, Jian
Publikováno v:
Medicine
Supplemental Digital Content is available in the text
Previous research identified SCN1B variants in some cases of Dravet syndrome (DS). We investigated whether SCN1B and SCN2B variants are commonly happened in DS patients without SCN1A variants
Previous research identified SCN1B variants in some cases of Dravet syndrome (DS). We investigated whether SCN1B and SCN2B variants are commonly happened in DS patients without SCN1A variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::979d73fb3ee94276bc1399adb27887f6
http://europepmc.org/articles/PMC6455785
http://europepmc.org/articles/PMC6455785
Publikováno v:
International Journal of Advancements in Computing Technology. 5:37-45
Based on the finite element method, Finite cell model of the stray current transmission net was established, and the mathematical expression of track potential, track current and stray current was proposed in the DC traction power system. And the ana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9330a496589229f1c35fda5c8d663555
https://doi.org/10.4156/ijact.vol5.issue3.5
https://doi.org/10.4156/ijact.vol5.issue3.5
Autor:
LIAO Hong-mei1,2, DAI Ling2 dailing55@yahoo. com. cn
Publikováno v:
Natural Product Research & Development. Aug2011, Vol. 23 Issue 4, p600-605. 6p.