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Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case report.
Published in:
2022
By:
- Fang, Jia;
- Huang, Hui;
- Lei, Qiang;
- Luo, Yingying;
- Tang, Zhengchu;
- Shi, Xiaoliu;
- Tang, Jian Guang
Publication type:
Case Study
Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case report.
Published in:
2022
By:
- Fang, Jia;
- Huang, Hui;
- Lei, Qiang;
- Luo, Yingying;
- Tang, Zhengchu;
- Shi, Xiaoliu;
- Tang, Jian Guang
Publication type:
journal article
BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage.
Published in:
Oxidative Medicine & Cellular Longevity, 2017, p. 1, doi. 10.1155/2017/5094934
By:
- Qin, Li-xia;
- Tan, Jie-qiong;
- Zhang, Hai-nan;
- Rizwana, Kousar;
- Lu, Jia-hong;
- Tang, Jian-guang;
- Jiang, Bo;
- Shen, Xiang-min;
- Guo, Ji-feng;
- Tang, Bei-sha;
- Tan, Li-ming;
- Wang, Chun-yu
Publication type:
Article
SUMO-1 Modification on K166 of PolyQ-Expanded aTaxin-3 Strengthens Its Stability and Increases Its Cytotoxicity.
Published in:
PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0054214
By:
- Ya-Fang Zhou;
- Shu-Sheng Liao;
- Ying-Ying Luo;
- Jian-Guang Tang;
- Jun-Ling Wang;
- Li-Fang Lei;
- Jing-Wei Chi;
- Juan Du;
- Hong Jiang;
- Kun Xia;
- Bei-Sha Tang;
- Lu Shen
Publication type:
Article
A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24.
Published in:
Human Genetics, 2004, v. 114, n. 6, p. 527, doi. 10.1007/s00439-004-1102-1
By:
- Bei-sha Tang;
- Wei Luo;
- Kun Xia;
- Jian-feng Xiao;
- Hong Jiang;
- Lu Shen;
- Jian-guang Tang;
- Guo-hua Zhao;
- Fang Cai;
- Qian Pan;
- He-ping Dai;
- Qi-dong Yang;
- Jia-hui Xia;
- Oleg V. Evgrafov
Publication type:
Article
Preliminary Study of hsa-mir-626 Change in the Cerebrospinal Fluid in Parkinson's Disease.
Published in:
2021
By:
- Qin, Li-Xia;
- Tan, Jie-Qiong;
- Zhang, Hai-Nan;
- Tang, Jian-Guang;
- Jiang, Bo;
- Shen, Xiang-Min;
- Guo, Ji-Feng;
- Tan, Li-Ming;
- Tang, Beisha;
- Wang, Chun-Yu
Publication type:
journal article
TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large‐Sample Study.
Published in:
Movement Disorders, 2022, v. 37, n. 3, p. 545, doi. 10.1002/mds.28865
By:
- Tian, Wo‐Tu;
- Zhan, Fei‐Xia;
- Liu, Zhen‐Hua;
- Liu, Zhe;
- Liu, Qing;
- Guo, Xia‐Nan;
- Zhou, Zai‐Wei;
- Wang, Shi‐Ge;
- Liu, Xiao‐Rong;
- Jiang, Hong;
- Li, Xun‐Hua;
- Zhao, Guo‐Hua;
- Li, Hai‐Yan;
- Tang, Jian‐Guang;
- Bi, Guang‐Hui;
- Zhong, Ping;
- Yin, Xiao‐Meng;
- Liu, Tao‐Tao;
- Ni, Rui‐Long;
- Zheng, Hao‐Ran
Publication type:
Article
A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.
Published in:
Cytogenetic & Genome Research, 2017, v. 152, n. 1, p. 16, doi. 10.1159/000477428
By:
- Zeng, Hui;
- Tang, Jian-Guang;
- Yang, Yi-Feng;
- Tan, Zhi-Ping;
- Tan, Jie-Qiong
Publication type:
Article
Case Report: Mutant SCN9A Susceptible to Charcot Neuroarthropathy in a Patient With Congenital Insensitivity to Pain.
Published in:
Frontiers in Neuroscience, 2021, v. 15, p. 1, doi. 10.3389/fnins.2021.697167
By:
- Xie, Xiao-hui;
- Tang, Jian-guang;
- Liu, Zhong-hua;
- Peng, Shui-jiao;
- Yuan, Zhuang-zhuang;
- Gu, Heng;
- Hu, Yi-qiao;
- Tan, Zhi-ping
Publication type:
Article

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