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Journal of Neural Transmission (Vienna, Austria : 1996)|February 18, 2021
Neuronal intranuclear inclusion disease: recognition and updateXi Lu, Daojun HongCurrent Issues in Molecular Biology|July 23, 2025
The Frmpd3 Protein Regulates Susceptibility to Epilepsy by Combining with GRIP and GluA2Yan Jia, Jinqiong Zhan, Pengcheng Huang, et al.Journal of Pain Research|September 2, 2022
Familial Episodic Pain SyndromesYu Shen, Yilei Zheng, Daojun HongWorld Neurosurgery|February 21, 2023
Internal Carotid Artery Aneurysm Presenting as Lower Cranial Nerve PalsiesJing Lin, Li Zhou, Daojun HongBMC Neurology|May 1, 2026
Severe peripheral neuropathy secondary to acute intermittent porphyria caused by a rare HMBS gene mutation: a case reportYurun Li, Danhua Wang, Daojun HongClinical Neuropathology|October 24, 2022
Distal hereditary neuropathy associated with a novel mutation in alanyl-aminoacyl-tRNA synthetaseYuan Yuan, Daojun Hong, Xuguang Gao, et al.Clinical Neuropathology|May 1, 2012
Danon disease caused by two novel mutations of the LAMP2 gene: implications for two ends of the clinical spectrumDaojun Hong, Zhihong Shi, Zhaoxia Wang, et al.Molecular Biology Reports|January 22, 2022
NMMHC IIA triggered lipid metabolize reprogramming resulting in vascular endothelial cellular tight junction injuryYanni Lv, Daojun Hong, Longsheng Fu, et al.Brain and Behavior|April 21, 2020
FUS P525L mutation causing amyotrophic lateral sclerosis and movement disordersBinbin Zhou, Huan Wang, Yu Cai, et al.Clinical Neuropathology|October 11, 2016
Mitochondrial proteomics reveal potential targets involved in mitochondrial abnormalities of desminopathyYunqing Chen, Junjun Zheng, Shuyun Chen, et al.Pageof 92