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Channels (Austin, Tex.)|April 4, 2015
Mutations of SCN4A gene cause different diseases: 2 case reports and literature reviewXiao-li Liu, Xiao-jun Huang, Xing-hua Luan, et al.Neuromuscular Disorders : NMD|February 10, 2019
Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature reviewWo-Tu Tian, Xing-Hua Luan, Hai-Yan Zhou, et al.Channels (Austin, Tex.)|August 12, 2015
Myotonia congenita: novel mutations in CLCN1 geneXiao-Li Liu, Xiao-Jun Huang, Jun-Yi Shen, et al.Seizure|April 2, 2018
Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature reviewWo-Tu Tian, Xiao-Li Liu, Yang-Qi Xu, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|October 8, 2018
The study of exercise tests in paroxysmal kinesigenic dyskinesiaHai-Yan Zhou, Fei-Xia Zhan, Wo-Tu Tian, et al.Nature Cell Biology|February 25, 2026
PML targets and resolves structured protein inclusions to mitigate neurodegenerationYang Wang, Jia-Xin Zhu, Fei-Xia Zhan, et al.Annals of Clinical and Translational Neurology|May 4, 2021
GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathyJiaxi Yu, Xing-Hua Luan, Meng Yu, et al.Brain Imaging and Behavior|July 25, 2020
Altered structural and functional connectivity in CSF1R-related leukoencephalopathyFei-Xia Zhan, Ze-Yu Zhu, Qing Liu, et al.Translational Neurodegeneration|December 13, 2019
Clinicopathologic characterization and abnormal autophagy of CSF1R-related leukoencephalopathyWo-Tu Tian, Fei-Xia Zhan, Qing Liu, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 12, 2020
The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in ChinaXiao-Jun Huang, Shi-Ge Wang, Xia-Nan Guo, et al.Pageof 3