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Journal of the Chinese Medical Association : JCMA|April 23, 2013
A homozygous NOTCH3 mutation p.R544C and a heterozygous TREX1 variant p.C99MfsX3 in a family with hereditary small vessel disease of the brainBing-Wen Soong, Yi-Chu Liao, Pang-Hsien Tu, et al.
Neurology. Genetics|April 29, 2016
Spinocerebellar ataxia type 36 in the Han ChineseYi-Chung Lee, Pei-Chien Tsai, Yuh-Cherng Guo, et al.
Pain Practice : the Official Journal of World Institute of Pain|November 17, 2020
Altered Cortical Reorganization and Brain Functional Connectivity in Phantom Limb Pain: A Functional MRI StudyBi-Xin Zheng, Yan Yin, Hong Xiao, et al.
Clinical Neurology and Neurosurgery|October 25, 2011
Clinical and cellular characterization of two novel MPZ mutations, p.I135M and p.Q187PfsX63Kon-Ping Lin, Bing-Wen Soong, Ming-Hong Chang, et al.
Journal of Neurology|May 13, 2010
Cellular characterization of MPZ mutations presenting with diverse clinical phenotypesYi-Chung Lee, Kon-Ping Lin, Ming-Hong Chang, et al.
Plos One|April 22, 2015
Change in the cortical complexity of spinocerebellar ataxia type 3 appears earlier than clinical symptomsTzu-Yun Wang, Chii-Wen Jao, Bing-Wen Soong, et al.
Neuroimage. Clinical|December 13, 2016
CAG repeat length does not associate with the rate of cerebellar degeneration in spinocerebellar ataxia type 3Shang-Ran Huang, Yu-Te Wu, Chii-Wen Jao, et al.
Journal of the Neurological Sciences|April 4, 2006
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: two novel mutations in the NOTCH3 gene in ChineseYi-Chung Lee, An-Hang Yang, Hsiu-Chih Liu, et al.
Entropy (Basel, Switzerland)|December 3, 2020
Intra- and Inter-Modular Connectivity Alterations in the Brain Structural Network of Spinocerebellar Ataxia Type 3Chi-Wen Jao, Bing-Wen Soong, Tzu-Yun Wang, et al.
Scientific Reports|February 6, 2019
Modeling spinocerebellar ataxias 2 and 3 with iPSCs reveals a role for glutamate in disease pathologyChing-Yu Chuang, Chih-Chao Yang, Bing-Wen Soong, et al.
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