Zhao Guohua, M.D.


Medical School:Central South University, Xiangya School of Medicine, China

Academic Rank:Chief Physician 


Clinical / Research Interests

Neurodegenerative diseases and inherited disorders of the nervous system, especially Parkinson's disease.

Professional Highlights

Professional Appointments

Education Experience

Research Summary


Fang J, Jirsch J, Wang S, Zhou D, Mu J, An D, Si Y, Zhao G*. Neurologists' attitudes toward driving among people with epilepsy in China: A pilot electronic survey. Epilepsia and Behavior, 2019, 94:47-51. 

Xu H, Zhang C, Cao L, Zhang B, Chen B*, Zhao G*. ATL3 mutation in a Chinese family with hereditary sensory neuropathy type 1F. Journal of the Peripheral Nervous System, 2019, 24(1): 50-55. 

Wang K, Wu D, Zhang B, Zhao G*. Novel CCM1 and CCM2 gene variants in two Chinese families with cerebral cavemous malformation. Frontiers in Neurology, 2018, 9:1128.

Zhao G, Liu X, Zhang Q, Wang K*. PRRT2 mutations in a cohort of Chinese families with paroxysmal kinesigenic dyskinesia and genotype-phenotype correlation reanalysis in literatures. International Journal of Neuroscience, 2018, 128(8): 751-760. 

Zhao G, Song J, Yang M, Song X, Liu X*. A novel mutation of LRSAM1 in a Chinese family with Charcot-Marie-Tooth disease. Journal of the Peripheral Nervous System, 2018, 23(1):55-59. 

Zhao G, Chen F, Zhang Q*, Shen M*, Gao Z. Feature-based information filtering in visual working memory is impaired in Parkinson's disease. Neuropsychologia, 2018, 111:317-323. 

Zhao GH, Liu XM*. Clinical features and genotype-phenotype correlation analysis in patients with ATL1 mutations: a literature reanalysis. Translational Neurodegeneration, 2017, 6: 9.

Zhao G, Liu X*, Jiang P*. Identification of a novel SPG4 tandem base substitution in a Chinese hereditary spastic paraplegia family. Neurological Sciences, 2017, 38(5):903-905.

Zhao G, Zhu PP, Renvoisé B, Maldonado-Báez L, Park SH, Blackstone C*. Mammalian knock out cells reveal prominent roles for atlastin GTPases in ER network morphology. Experimental Cell Research, 2016, 349(1): 32-44.

Wang K, Zhao G*. Exon 8-17 deletions of SPAST in a Chinese family with hereditary spastic paraplegia: A case report and literature review. Journal of the Neurological Science, 2015, 357(1-2): 282-4.

Zhao G, Blackstone C*. ER Morphology: Sculpting with XendoU. Current Biology, 2014, 24(24): R1170-1172. 

Wu JY, Zhang BR, Zhao GH*. Cerebral infarction and cranial venous sinus thrombosis caused by paragonimiasis. CNS Neuroscience Therapeutics, 2013, 19(9): 734-736. 

Zhao GH, Yin XZ, Wu DW, Mao SY, Yin H, Zhang BR*. Clinical features and Cu/Zn superoxide dismutase gene mutations in two Mainland Chinese families with amyotrophic lateral sclerosis. International Journal of Neuroscience, 2011, 121(4): 191-195.

Yin XZ, Liu JR, Zhang BR, Zhang L, Wang PZ, Zhou FY, Ding MP, Zhao GH*. Report of two Chinese families and a review of Chinese CADASIL patients. Journal of the Neurological Sciences, 2009, 279(1-2): 88-92. 

Zhao G, Ding M, Zhang B, Lv W, Yin H, Zhang L, Ying Z, Zhang Q*. Clinical manifestations and management of acute thallium poisoning. European Neurology, 2008, 60(6): 292-297.

Zhao G, Hu Z, Shen L, Jiang H, Ren ZJ, Liu XM, Xia K, Guo P, Pan Q, Tang BS*. A novel candidate locus on chromosome 11p14.1-p11.2 for autosomal dominant hereditary spastic paraplegia. Chinese Medical Journal, 2008, 121(5): 430-434. 

Tang B*, Zhao G, Luo W, et al. Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L. Human Genetics, 2005, 116(3): 222-224.

Tang B*, Zhao G, Xia K, et al. Three novel mutations of the spastin gene in Chinese patients with hereditary spastic paraplegia. Archives of Neurology, 2004, 61(1): 49-55.

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