W. Gu

发表

Molecular and clinical study of spinocerebellar ataxia type 7 in Chinese kindreds.

Y. Zhou, B. Zhou, G. Wang, 2000, Archives of neurology.

Recommendations for the diagnosis and treatment of paroxysmal kinesigenic dyskinesia: an expert consensus in China

Zhaoxia Wang, Shengdi Chen, B. Tang, 2021, Translational Neurodegeneration.

Spinocerebellar ataxia 17: Inconsistency between phenotype and neuroimage findings

W. Gu, Y. Hao, Jin Zhang, 2013, Annals of Indian Academy of Neurology.

A Novel Asp121Asn Mutation of Myelin Protein Zero Is Associated with Late-Onset Axonal Charcot-Marie-Tooth Disease, Hearing Loss and Pupil Abnormalities

D. Fan, J. Jiao, H. Wen, 2016, Front. Aging Neurosci..

Clinical phenotype and genetic mutation of one case with head tremor and cerebellar atrophy

Kunpeng Xie, W. Gu, Y. Hao, 2017 .

Autosomal Recessive Cerebellar Ataxia Type 1: Phenotypic and Genetic Correlation in a Cohort of Chinese Patients with SYNE1 Variants

X. Duan, Ren-bin Wang, W. Gu, 2020, The Cerebellum.

Characterization of genotype–phenotype correlation with MORC2 mutated Axonal Charcot–Marie–Tooth disease in a cohort of Chinese patients

Yuting Zhang, Jing Li, Guochun Wang, 2021, Orphanet Journal of Rare Diseases.

Spinocerebellar ataxia type 10 in Chinese Han

T. Ashizawa, G. Xia, C. Mulligan, 2015, Neurology: Genetics.

Autosomal Recessive Cerebellar Ataxia Type 1: Phenotypic and Genetic Correlation in a Cohort of Chinese Patients with SYNE1 Variants

X. Duan, Ren-bin Wang, W. Gu, 2020, The Cerebellum.

Identification of a Splicing Mutation in ITPR1 via WES in a Chinese Early-Onset Spinocerebellar Ataxia Family

W. Gu, Y. Hao, Zhenhua Cao, 2017, The Cerebellum.

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.

Non-motor symptoms in multiple system atrophy: A comparative study with Parkinson's disease and progressive supranuclear palsy

P. H. Hopchev, Yue Huang, Jinghong Ma, 2023, Frontiers in Neurology.

Spinocerebellar ataxia type 1 in China: molecular analysis and genotype-phenotype correlation in 5 families.

S. Tsuji, B. Tang, Y. Takiyama, 2001, Archives of neurology.

Identification of a Splicing Mutation in ITPR1 via WES in a Chinese Early-Onset Spinocerebellar Ataxia Family

Peng Yu, W. Gu, Y. Hao, 2017, The Cerebellum.

The Shortest Expanded Allele of the MJD1 Gene in a Chinese MJD Kindred with Autonomic Dysfunction

Yan Shen, M. Jin, Xingzhou Liu, 2004, European Neurology.

Clinical and genetic study of ataxia with isolated vitamin E deficiency

W. Gu, Y. Hao, Yuan-yuan Chen, 2014 .

Genome-wide association study identifies a new susceptibility locus in PLA2G4C for Multiple System Atrophy.

Sonja W. Scholz, A. Singleton, Y. Kusakabe, 2023, medRxiv.

Huntingtin gene CAG repeat numbers in Chinese patients with Huntington's disease and controls

J. Burgunder, Z. Pei, H. Jiang, 2014, European journal of neurology.