1. A novel CPT1C variant causes pure hereditary spastic paraplegia with benign clinical course. Issue 3 (4th January 2019) Authors: Hong, Daojun; Cong, Lu; Zhong, Shanshan; Liu, Ling; Xu, Yan; Zhang, Jun Journal: Annals of clinical and translational neurology Issue: Volume 6:Issue 3(2019) Page Start: 610 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel KIF5A gene variant causes spastic paraplegia and cerebellar ataxia. Issue 11 (17th September 2018) Authors: Qiu, Yusen; Zhong, Shanshan; Cong, Lu; Xin, Ling; Gao, Xuguang; Zhang, Jun; Hong, Daojun Journal: Annals of clinical and translational neurology Issue: Volume 5:Issue 11(2018) Page Start: 1415 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Application of quantitative EEG in acute ischemic stroke patients who underwent thrombectomy: A comparison with CT perfusion. (September 2022) Authors: Zhang, Na; Chen, Fangmei; Xie, Xufang; Xie, Zunchun; Hong, Daojun; Li, Jun; Ouyang, Taohui Journal: Clinical neurophysiology Issue: Volume 141(2022) Page Start: 24 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Autophagic vacuolar myopathy involving the phenotype of spinocerebellar ataxia type 3. Issue 2 (17th August 2022) Authors: Li, Jingjing; Peng, Yun; Tang, Jincai; Li, Menghua; Zhu, Min; Zhou, Meihong; Fang, Pu; Hong, Daojun Journal: Neuropathology Issue: Volume 43:Issue 2(2023) Page Start: 135 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Benign monomelic amyotrophy of lower limb in a cohort of chinese patients. Issue 4 (2nd March 2021) Authors: Wang, Lulu; Wen, Han; Chen, Shuyun; Wang, Huan; Zheng, Yilei; Chen, Ran; Li, Jingjing; Jiang, Kaiyan; Xiang, Haijie; Zhu, Min; Zhou, Meihong; Yao, Sheng; Hong, Daojun Journal: Brain and behavior Issue: Volume 11:Issue 4(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Both hypokalaemic and normokalaemic periodic paralysis in different members of a single family with novel R1129Q mutation in SCN4A gene. Issue 6 (3rd June 2010) Authors: Hong, Daojun; Luan, Xinghua; Chen, Bin; Zheng, Riliang; Zhang, Wei; Wang, Zhaoxia; Yuan, Yun Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 81:Issue 6(2010) Page Start: 703 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Diverse myopathological features in the congenital myasthenia syndrome with GFPT1 mutation. Issue 2 (3rd January 2022) Authors: Jiang, Kaiyan; Zheng, Yilei; Lin, Jing; Wu, Xiaorong; Yu, Yanyan; Zhu, Min; Fang, Xin; Zhou, Meihong; Li, Xiaobing; Hong, Daojun Journal: Brain and behavior Issue: Volume 12:Issue 2(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Fasting blood glucose as a predictor of progressive infarction in men with acute ischemic stroke. Issue 10 (October 2022) Authors: Yu, Qiulong; Mao, Xiaocheng; Fu, Zhihui; Luo, Si; Huang, Qin; Chen, Qianxi; Li, Shumeng; Zhang, Jinchong; Qiu, Yuexin; Wu, Yuhang; Fang, Pu; Hong, Daojun; Lin, Jing Journal: Journal of international medical research Issue: Volume 50:Issue 10(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. FUS P525L mutation causing amyotrophic lateral sclerosis and movement disorders. Issue 6 (19th April 2020) Authors: Zhou, Binbin; Wang, Huan; Cai, Yu; Wen, Han; Wang, Lulu; Zhu, Min; Chen, Yunqing; Yu, Yanyan; Lu, Xi; Zhou, Meihong; Fang, Pu; Li, Xiaobing; Hong, Daojun Journal: Brain and behavior Issue: Volume 10:Issue 6(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease. Issue 5 (25th March 2021) Authors: Deng, Jianwen; Zhou, Binbin; Yu, Jiaxi; Han, Xiaochen; Fu, Jianhui; Li, Xiaobin; Xie, Xufang; Zhu, Min; Zheng, Yilei; Guo, Xueyu; Li, Pidong; Wang, Qingqing; Liu, Jing; Zhang, Wei; Yuan, Yun; Yao, Sheng; Wang, Zhaoxia; Hong, Daojun Journal: Journal of medical genetics Issue: Volume 59:Issue 5(2022) Page Start: 462 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗