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Chengqing Yang

Showing results (31-40 of 58) with videos related to

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International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|March 20, 2021
Report of a case with ferredoxin reductase (FDXR) gene variants in a Chinese boy exhibiting hearing loss, visual impairment, and motor retardationChengqing Yang, Ying Zhang, Jiuwei Li, et al.
Journal of Molecular Neuroscience : MN|June 16, 2019
Association of the Polymorphism of rs1799822 on Carnitine Palmitoyltransferase II Gene with Severe Enterovirus 71 Encephalitis in Chinese ChildrenYa Guo, Yu Zhang, Peipei Liu, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|October 2, 2018
The biochemical characterization of a missense mutation m.8914C>T in ATP6 gene associated with mitochondrial encephalomyopathyYa Guo, Yu Zhang, Fei Li, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|August 17, 2019
Levodopa is effective in the treatment of three Chinese Tyrosine hydroxylase (TH) deficiency childrenMei Hou, Chengqing Yang, Jingfei Hu, et al.
BMC Medical Genomics|October 15, 2022
A heterozygous missense variant in the YWHAG gene causing developmental and epileptic encephalopathy 56 in a Chinese familyZhi Yi, Zhenfeng Song, Jiao Xue, et al.
Immunity, Inflammation and Disease|November 29, 2022
TMEM173 rs7447927 genetic polymorphism and susceptibility to severe enterovirus 71 infection in Chinese childrenJie Song, Yedan Liu, Ya Guo, et al.
Brain and Behavior|August 1, 2021
A cohort study of mild encephalitis/encephalopathy with a reversible splenial lesion in childrenJiao Xue, Ying Zhang, Jie Kang, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|April 1, 2018
A case of Pitt-hopkins Syndrome with de novo mutation in TCF4: Clinical features and treatment for epilepsyYedan Liu, Ya Guo, Peipei Liu, et al.
Nordic Journal of Psychiatry|March 4, 2015
Effect of time and duration of untreated psychosis on cognitive and social functioning in Chinese patients with first-episode schizophrenia: A 1-year studyAnisha Heeramun-Aubeeluck, Na Liu, Felix Fischer, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|February 8, 2018
Oligoadenylate synthetase 3 S381R gene polymorphism is associated with severity of EV71 infection in Chinese childrenYedan Liu, Peipei Liu, Shihai Liu, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|March 20, 2021
Report of a case with ferredoxin reductase (FDXR) gene variants in a Chinese boy exhibiting hearing loss, visual impairment, and motor retardationChengqing Yang, Ying Zhang, Jiuwei Li, et al.
Journal of Molecular Neuroscience : MN|June 16, 2019
Association of the Polymorphism of rs1799822 on Carnitine Palmitoyltransferase II Gene with Severe Enterovirus 71 Encephalitis in Chinese ChildrenYa Guo, Yu Zhang, Peipei Liu, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|October 2, 2018
The biochemical characterization of a missense mutation m.8914C>T in ATP6 gene associated with mitochondrial encephalomyopathyYa Guo, Yu Zhang, Fei Li, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|August 17, 2019
Levodopa is effective in the treatment of three Chinese Tyrosine hydroxylase (TH) deficiency childrenMei Hou, Chengqing Yang, Jingfei Hu, et al.
BMC Medical Genomics|October 15, 2022
A heterozygous missense variant in the YWHAG gene causing developmental and epileptic encephalopathy 56 in a Chinese familyZhi Yi, Zhenfeng Song, Jiao Xue, et al.
Immunity, Inflammation and Disease|November 29, 2022
TMEM173 rs7447927 genetic polymorphism and susceptibility to severe enterovirus 71 infection in Chinese childrenJie Song, Yedan Liu, Ya Guo, et al.
Brain and Behavior|August 1, 2021
A cohort study of mild encephalitis/encephalopathy with a reversible splenial lesion in childrenJiao Xue, Ying Zhang, Jie Kang, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|April 1, 2018
A case of Pitt-hopkins Syndrome with de novo mutation in TCF4: Clinical features and treatment for epilepsyYedan Liu, Ya Guo, Peipei Liu, et al.
Nordic Journal of Psychiatry|March 4, 2015
Effect of time and duration of untreated psychosis on cognitive and social functioning in Chinese patients with first-episode schizophrenia: A 1-year studyAnisha Heeramun-Aubeeluck, Na Liu, Felix Fischer, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|February 8, 2018
Oligoadenylate synthetase 3 S381R gene polymorphism is associated with severity of EV71 infection in Chinese childrenYedan Liu, Peipei Liu, Shihai Liu, et al.
Pageof 6