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Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|August 6, 2013
Cerebral sparganosis in mainland Chinese patientsDaojun Hong, Huiqun Xie, Min Zhu, et al.
Clinical Neuropathology|June 2, 2022
<i>DNAJB2</i> c.184C>T mutation associated with distal hereditary motor neuropathy with rimmed vacuolar myopathyMeige Liu, Yan Xu, Daojun Hong, et al.
BMC Neurology|November 12, 2013
Sturge-Weber syndrome coexisting with episodes of rhabdomyolysisMin Zhu, Xiaobin Li, Meihong Zhou, et al.
Current 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.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|January 31, 2015
[Clinical features of familial idiopathic basal ganglia calcification caused by a novel mutation in the SLC20A2 gene]Min Zhu, Cheng Fang, Xiaobing Li, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 21, 2022
TMEM151A phenotypic spectrum includes paroxysmal kinesigenic dyskinesia with infantile convulsionsHuan Wang, Pengcheng Huang, Min Zhu, et al.
Nutrients|November 26, 2022
Neurotrophic Role of the Next-Generation Probiotic Strain <i>L. lactis</i> MG1363-pMG36e-GLP-1 on Parkinson's Disease via Inhibiting FerroptosisMengyun Yue, Jing Wei, Wenjie Chen, et al.
Annals of Clinical and Translational Neurology|March 27, 2019
A novel <i>CPT1C</i> variant causes pure hereditary spastic paraplegia with benign clinical courseDaojun Hong, Lu Cong, Shanshan Zhong, et al.
BMC Neurology|May 11, 2015
Diffuse leptomeningeal gliomatosis initially presenting with intraventricular hemorrhage: a case report and literature reviewMin Zhu, JunJun Zheng, Yuanzhao Zhu, et al.
Clinical Neuropathology|October 6, 2012
A novel heterozygous deletion-insertion mutation in the desmin gene causes complete atrioventricular block and mild myopathyLingling Cao, Daojun Hong, Min Zhu, et al.
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