Guo-Hua Zhao

发表

Study of Methylation Levels of Parkin Gene Promoter in Parkinson's Disease Patients

Bao-Rong Zhang, W. Luo, M. Cai, 2011, The International journal of neuroscience.

The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China

Huidong Tang, S. Chen, Wotu Tian, 2020, Movement disorders : official journal of the Movement Disorder Society.

Mutation analysis of parkin and PINK1 genes in early-onset Parkinson's disease in China

W. Luo, Zhi-rong Liu, M. Cai, 2010, Neuroscience Letters.

Hemichorea due to ipsilateral thalamic infarction: A case report

Guo-Hua Zhao, Jiajia Fang, Zhao-Sheng Li, 2021, World journal of clinical cases.

TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large‐Sample Study

B. Tang, Qing Liu, Wotu Tian, 2021, Movement disorders : official journal of the Movement Disorder Society.

Report of two Chinese families and a review of Mainland Chinese CADASIL patients

Mei-Ping Ding, Guo-Hua Zhao, Jian-ren Liu, 2009, Journal of the Neurological Sciences.

Hyperglycemic hemianopia: A case report

Guo-Hua Zhao, Jiajia Fang, Xiao-Hui Xiang, 2021, World journal of clinical cases.

Clinical features and genotype-phenotype correlation analysis in patients with ATL1 mutations: A literature reanalysis

Guo-Hua Zhao, Xiao-min Liu, 2017, Translational Neurodegeneration.

Mutation analysis of small heat-shock protein 22 gene in Chinese patients with Charcot-Marie-Tooth disease.

C. Zhang, K. Xia, B. Tang, 2005, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

[The characteristics of gene mutations in Chinese patients with Charcot-Marie-Tooth disease].

K. Xia, Q. Pan, B. Tang, 2005, Zhonghua yi xue za zhi.

Hypereosinophilia with cerebral venous sinus thrombosis and intracerebral hemorrhage: A case report and review of the literature

Guo-Hua Zhao, Xiuhua Song, Tian-ming Xu, 2021, World journal of clinical cases.

[Gene screening in five Chinese families with hereditary spastic paraplegia with thin corpus callosum].

K. Xia, B. Tang, Lu Shen, 2007, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Clinical features of hereditary spastic paraplegia with thin corpus callosum: report of 5 Chinese cases.

B. Tang, W. Luo, Hong Jiang, 2004, Chinese medical journal.

MiR-200c-3p Regulates DUSP1/MAPK Pathway in the Nonalcoholic Fatty Liver After Laparoscopic Sleeve Gastrectomy

Guo-Hua Zhao, Yong Wang, Xiuming Miao, 2022, Frontiers in Endocrinology.

Gallic acid inhibits Kaposi's Sarcoma‐associated herpesvirus lytic reactivation by suppressing RTA transcriptional activities

Y. Liu, Guo-Hua Zhao, Yao Wu, 2020, Food science & nutrition.

Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L

K. Xia, Q. Pan, H. Dai, 2005, Human Genetics.

Coding mutations in NUS1 contribute to Parkinson’s disease

H. Shang, P. Chan, K. Xia, 2018, Proceedings of the National Academy of Sciences.

Cerebral Infarction and Cranial Venous Sinus Thrombosis Caused by Paragonimiasis

Guo-Hua Zhao, Bao‐Rong Zhang, Jia-Yan Wu, 2013, CNS neuroscience & therapeutics.

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24

K. Xia, Q. Pan, H. Dai, 2004, Human Genetics.

[Mutation analysis of LITAF, RAB7, LMNA and MTMR2 genes in Chinese Charcot-Marie-Tooth disease.].

K. Xia, B. Tang, Zhengmao Hu, 2010, Yi chuan = Hereditas.

CCG polymorphisms in the huntingtin gene have no effect on the pathogenesis of patients with Huntington's disease in mainland Chinese families

K. Xia, B. Tang, Jun Tian, 2012, Journal of the Neurological Sciences.

Hesperetin inhibits KSHV reactivation and is reversed by HIF1α overexpression.

Guo-Hua Zhao, Yao Wu, Wen-Ying Long, 2021, The Journal of general virology.

Chinese patient with cerebrotendinous xanthomatosis confirmed by genetic testing: A case report and literature review

Guo-Hua Zhao, Y. Liu, Lanxiao Cao, 2020, World journal of clinical cases.

Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Chinese Han patients with hereditary spastic paraplegia.

K. Xia, B. Tang, Hong Jiang, 2009, Chinese medical journal.

Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1

K. Xia, B. Tang, Hong Jiang, 2011, Clinical Neurology and Neurosurgery.

Compound heterozygous mutations in the neuraminidase 1 gene in type 1 sialidosis: A case report and review of literature

Guo-Hua Zhao, Y. Liu, Lanxiao Cao, 2021, World journal of clinical cases.

Clinical features and genotype-phenotype correlation analysis in patients with ATL1 mutations: A literature reanalysis

Guo-Hua Zhao, Xiao-min Liu, 2017, Translational Neurodegeneration.

[Frequency analysis of autosomal dominant spinocerebellar ataxias in Han population in the Chinese mainland and clinical and molecular characterization of spinocerebellar ataxia type 6].

K. Xia, B. Tang, Hong Jiang, 2005, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

An association between the PARK16 locus and Parkinson's disease in a cohort from eastern China.

Jun Tian, Guo-Hua Zhao, Yaping Yan, 2011, Parkinsonism & related disorders.

A novel candidate locus on chromosome 11p14.1-p11.2 for autosomal dominant hereditary spastic paraplegia.

K. Xia, Q. Pan, B. Tang, 2008, Chinese medical journal.

Endoplasmic Reticulum-Shaping Atlastin Proteins Facilitate KSHV Replication

Guo-Hua Zhao, Yao Wu, Wen-Ying Long, 2022, Frontiers in Cellular and Infection Microbiology.

Research on screening and identification of proteins interacting with ataxin-3.

K. Xia, Q. Pan, B. Tang, 2005, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.