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LiYing Cui

Showing results (141-150 of 323) with videos related to

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Frontiers in Neurology|July 1, 2022
Long-Term Efficacy of Non-steroid Immunosuppressive Agents in Anti-Muscle-Specific Kinase Positive Myasthenia Gravis Patients: A Prospective StudyYing Tan, Jiayu Shi, Yangyu Huang, et al.
Plos One|September 15, 2015
Cognitive Impairment in Chinese Patients with Sporadic Amyotrophic Lateral SclerosisBo Cui, Liying Cui, Jing Gao, et al.
Muscle & Nerve|July 2, 2016
Needle electromyography of the frontalis muscle in patients with amyotrophic lateral sclerosisHua Pan, Fan Jian, Jinxi Lin, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 5, 2019
A therapeutic regimen for 3-hydroxyisobutyryl-CoA hydrolase deficiency with exercise-induced dystoniaYan Xu, Jing Zhang, Kang Yu, et al.
Journal of Neurochemistry|March 4, 2023
Astrocytic purinergic signalling contributes to the development and maintenance of neuropathic pain via modulation of glutamate releaseSuting Liu, Hao Cheng, Liying Cui, et al.
Frontiers of Medicine|March 16, 2024
Dysregulated N<sup>6</sup>-methyladenosine modification in peripheral immune cells contributes to the pathogenesis of amyotrophic lateral sclerosisDi He, Xunzhe Yang, Liyang Liu, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|July 6, 2019
Motor conduction block and conduction velocity in Lewis-Sumner syndrome and multifocal motor neuropathyYi Li, Jingwen Niu, Tanxin Liu, et al.
Neuromuscular Disorders : NMD|May 20, 2015
A comprehensive genetic diagnosis of Chinese muscular dystrophy and congenital myopathy patients by targeted next-generation sequencingYi Dai, Xiaoming Wei, Yanhuan Zhao, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 18, 2010
Restoration of domain folding and interdomain assembly by second-site suppressors of the DeltaF508 mutation in CFTRLihua He, Luba A Aleksandrov, Liying Cui, et al.
Neurology India|May 15, 2014
Morvan syndrome plus thyroid dysfunction: a case with chronic mercury exposureYifan Li, Haitao Ren, Ming Ren, et al.
Pageof 33

Showing results (141-150 of 323) with videos related to

Sort By:
Pageof 33
Frontiers in Neurology|July 1, 2022
Long-Term Efficacy of Non-steroid Immunosuppressive Agents in Anti-Muscle-Specific Kinase Positive Myasthenia Gravis Patients: A Prospective StudyYing Tan, Jiayu Shi, Yangyu Huang, et al.
Plos One|September 15, 2015
Cognitive Impairment in Chinese Patients with Sporadic Amyotrophic Lateral SclerosisBo Cui, Liying Cui, Jing Gao, et al.
Muscle & Nerve|July 2, 2016
Needle electromyography of the frontalis muscle in patients with amyotrophic lateral sclerosisHua Pan, Fan Jian, Jinxi Lin, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 5, 2019
A therapeutic regimen for 3-hydroxyisobutyryl-CoA hydrolase deficiency with exercise-induced dystoniaYan Xu, Jing Zhang, Kang Yu, et al.
Journal of Neurochemistry|March 4, 2023
Astrocytic purinergic signalling contributes to the development and maintenance of neuropathic pain via modulation of glutamate releaseSuting Liu, Hao Cheng, Liying Cui, et al.
Frontiers of Medicine|March 16, 2024
Dysregulated N<sup>6</sup>-methyladenosine modification in peripheral immune cells contributes to the pathogenesis of amyotrophic lateral sclerosisDi He, Xunzhe Yang, Liyang Liu, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|July 6, 2019
Motor conduction block and conduction velocity in Lewis-Sumner syndrome and multifocal motor neuropathyYi Li, Jingwen Niu, Tanxin Liu, et al.
Neuromuscular Disorders : NMD|May 20, 2015
A comprehensive genetic diagnosis of Chinese muscular dystrophy and congenital myopathy patients by targeted next-generation sequencingYi Dai, Xiaoming Wei, Yanhuan Zhao, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 18, 2010
Restoration of domain folding and interdomain assembly by second-site suppressors of the DeltaF508 mutation in CFTRLihua He, Luba A Aleksandrov, Liying Cui, et al.
Neurology India|May 15, 2014
Morvan syndrome plus thyroid dysfunction: a case with chronic mercury exposureYifan Li, Haitao Ren, Ming Ren, et al.
Pageof 33