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Novel mutations in the SPAST gene cause hereditary spastic paraplegia.
Zhu Z, Zhang C, Zhao G, Liu Q, Zhong P, Zhang M, Tang W, Zhan F, Tian W, Wang Y, Yin K, Huang X, Jiang J, Liu X, Liu S, Zhou H, Luan X, Tang H, Wang Y, Chen S, Cao L. Zhu Z, et al. Among authors: zhong p. Parkinsonism Relat Disord. 2019 Dec;69:125-133. doi: 10.1016/j.parkreldis.2019.11.007. Epub 2019 Nov 6. Parkinsonism Relat Disord. 2019. PMID: 31751864
The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China.
Huang XJ, Wang SG, Guo XN, Tian WT, Zhan FX, Zhu ZY, Yin XM, Liu Q, Yin KL, Liu XR, Zhang Y, Liu ZG, Liu XL, Zheng L, Wang T, Wu L, Rong TY, Wang Y, Zhang M, Bi GH, Tang WG, Zhang C, Zhong P, Wang CY, Tang JG, Lu W, Zhang RX, Zhao GH, Li XH, Li H, Chen T, Li HY, Luo XG, Song YY, Tang HD, Luan XH, Zhou HY, Tang BS, Chen SD, Cao L. Huang XJ, et al. Among authors: zhong p. Mov Disord. 2020 Aug;35(8):1428-1437. doi: 10.1002/mds.28061. Epub 2020 May 11. Mov Disord. 2020. PMID: 32392383
Clinicopathologic characterization and abnormal autophagy of CSF1R-related leukoencephalopathy.
Tian WT, Zhan FX, Liu Q, Luan XH, Zhang C, Shang L, Zhang BY, Pan SJ, Miao F, Hu J, Zhong P, Liu SH, Zhu ZY, Zhou HY, Sun S, Liu XL, Huang XJ, Jiang JW, Ma JF, Wang Y, Chen SF, Tang HD, Chen SD, Cao L. Tian WT, et al. Among authors: zhong p. Transl Neurodegener. 2019 Dec 2;8:32. doi: 10.1186/s40035-019-0171-y. eCollection 2019. Transl Neurodegener. 2019. PMID: 31827782 Free PMC article.
Expanding the clinical spectrum of adult-onset neuronal intranuclear inclusion disease.
Cao Y, Wu J, Yue Y, Zhang C, Liu S, Zhong P, Wang S, Huang X, Deng W, Pan J, Zheng L, Liu Q, Shang L, Zhang B, Yang J, Chen G, Chen S, Cao L, Luan X. Cao Y, et al. Among authors: zhong p. Acta Neurol Belg. 2022 Jun;122(3):647-658. doi: 10.1007/s13760-021-01622-4. Epub 2021 Feb 24. Acta Neurol Belg. 2022. PMID: 33625684
1,039 results