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CORC

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Autoantibody against the Rab6A/Rab6B in primary autoimmune cerebellar ataxia associated with Sjogren's syndrome: A case report 期刊论文
JOURNAL OF NEUROIMMUNOLOGY, 2021, 卷号: 359, 页码: 7
作者:  Guo, Liyuan;  Ren, Haitao;  Fan, Siyuan;  Guan, Hongzhi;  Wang, Jing
收藏  |  浏览/下载：43/0  |  提交时间：2021/10/29
Cerebellar ataxia and myeloradiculopathy associated with AP3B2 antibody: a case report and literature review 期刊论文
JOURNAL OF NEUROLOGY, 2021, 页码: 7
作者:  Mange, Liu;  Haitao, Ren;  Lixin, Zhou;  Siyuan, Fan;  Jing, Wang
收藏  |  浏览/下载：52/0  |  提交时间：2021/06/09
Neurochondrin Antibody Serum Positivity in Three Cases of Autoimmune Cerebellar Ataxia 期刊论文
CEREBELLUM, 2019, 卷号: 18, 期号: 6, 页码: 1137-1142
作者:  Zhang Weihua;  Ren Haitao;  Fang Fang;  Yang Xunzhe;  Wang Jing
收藏  |  浏览/下载：63/0  |  提交时间：2020/02/29
Metabolic Profiling Reveals Biochemical Pathways and Potential Biomarkers of Spinocerebellar Ataxia 3 期刊论文
FRONTIERS IN MOLECULAR NEUROSCIENCE, 2019, 卷号: 12, 页码: 10
作者:  Yang, Zhi-hua;  Shi, Chang-he;  Zhou, Li-na;  Li, Yu-sheng;  Yang, Jing
收藏  |  浏览/下载：85/0  |  提交时间：2019/12/02
Anti-Homer-3 antibody associated cerebellar ataxia: A rare case report and literature review 期刊论文
JOURNAL OF NEUROIMMUNOLOGY, 2019, 卷号: 330, 页码: 155-158
作者:  Xu, Xiaolu;  Ren, Haitao;  Li, Libo;  Wang, Jing;  Fechner, Kai
收藏  |  浏览/下载：54/0  |  提交时间：2019/05/20
Identification of a novel mutation in the CACNA1C gene in a Chinese family with autosomal dominant cerebellar ataxia 期刊论文
BMC NEUROLOGY, 2019, 卷号: 19
作者:  Chen, Jiajun;  Sun, Yajuan;  Liu, Xiaoyang;  Li, Jia
收藏  |  浏览/下载：31/0  |  提交时间：2019/12/05
Ataxia as the main manifestation of tumor-like primary angiitis of the central nervous system: a case report and literature review 期刊论文
BMC MEDICAL IMAGING, 2019, 卷号: 19, 期号: 1
作者:  Zhang, Li;  Huang, Yu-Jing;  Nan, Guang-Xian;  Mao, Ying
收藏  |  浏览/下载：10/0  |  提交时间：2019/12/05
Gerstmann-Straussler-Scheinker disease: A case report 期刊论文
WORLD JOURNAL OF CLINICAL CASES, 2019, 卷号: 7, 期号: 3
作者:  Zhao, Ming-Ming;  Feng, Liang-Shu;  Hou, Shuai;  Shen, Ping-Ping;  Cui, Li
收藏  |  浏览/下载：7/0  |  提交时间：2019/12/05
Two novel homozygous mutations of CAPN1 in Chinese patients with hereditary spastic paraplegia and literatures review 期刊论文
ORPHANET JOURNAL OF RARE DISEASES, 2019, 卷号: 14
作者:  Peng, Fang;  Sun, Yi-Min;  Quan, Chao;  Wang, Jian;  Wu, Jian-Jun
收藏  |  浏览/下载：9/0  |  提交时间：2019/12/05
Novel homozygous ataxia-telangiectasia (A-T) mutated gene mutation identified in a Chinese pedigree with A-T 期刊论文
MOLECULAR MEDICINE REPORTS, 2019, 卷号: 20, 期号: 2
作者:  Hu, Huifang;  Chen, Weicheng;  Liu, Sida;  Chen, Gang;  Zhu, Shaicheng
收藏  |  浏览/下载：28/0  |  提交时间：2019/12/05

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