X. Hou

发表

Alterations of the Gut Microbiota in Multiple System Atrophy Patients

K. Xia, B. Tang, Hong Jiang, 2019, Front. Neurosci..

Analysis of (CAG)n expansion in ATXN1, ATXN2 and ATXN3 in Chinese patients with multiple system atrophy

K. Xia, H. Peng, B. Tang, 2018, Scientific Reports.

Biallelic Intronic AAGGG Expansion of RFC1 is Related to Multiple System Atrophy

T. Ashizawa, K. Xia, B. Tang, 2020, Annals of neurology.

Central motor conduction time in spinocerebellar ataxia: a meta-analysis

B. Tang, Hong Jiang, Linlin Wan, 2020, Aging.

Evaluation of Peripheral Immune Activation in Amyotrophic Lateral Sclerosis

K. Xia, B. Tang, Ji-feng Guo, 2020, Frontiers in Neurology.

Genetic etiology of a Chinese ataxia cohort: Expanding the mutational spectrum of hereditary ataxias.

K. Xia, B. Tang, Hong Jiang, 2021, Parkinsonism & related disorders.

No genetic evidence for the involvement of GGC repeat expansions of the NOTCH2NLC gene in Chinese patients with multiple system atrophy

B. Tang, Hong Jiang, Linlin Wan, 2020, Neurobiology of Aging.

C9orf72 hexanucleotide expansion analysis in Chinese patients with multiple system atrophy.

K. Xia, B. Tang, Hong Jiang, 2015, Parkinsonism & related disorders.

[1H-proton magnetic resonance spectroscopy in patients with multiple system atrophy and  cognitive dysfunction].

B. Tang, Hong Jiang, Gaofeng Zhou, 2015, Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences.

The Natural History of Spinocerebellar Ataxia Type 3 in Mainland China: A 2-Year Cohort Study

T. Klockgether, K. Xia, B. Tang, 2022, Frontiers in Aging Neuroscience.

Posterior reversible encephalopathy syndrome with involvement of the cervical cord and medulla: a case report.

Hong Jiang, X. Hou, Jinfeng Xu, 2015, Journal of clinical and diagnostic research : JCDR.

New Model for Estimation of the Age at Onset in Spinocerebellar Ataxia Type 3

T. Klockgether, K. Xia, Jinchen Li, 2021, Neurology.

Association of TNF-α rs1799964 and IL-1β rs16944 polymorphisms with multiple system atrophy in Chinese Han population

K. Xia, B. Tang, Hong Jiang, 2018, The International journal of neuroscience.

Identification of GGC repeat expansion in the NOTCH2NLC gene in amyotrophic lateral sclerosis

B. Tang, Hong Jiang, Lu Shen, 2020, Neurology.

Two Novel SNPs in ATXN3 3’ UTR May Decrease Age at Onset of SCA3/MJD in Chinese Patients

T. Ashizawa, K. Xia, Q. Pan, 2015, PloS one.

Clinical features of NOTCH2NLC-related neuronal intranuclear inclusion disease

B. Tang, Ji-feng Guo, Q. Xiao, 2022, Journal of Neurology, Neurosurgery, and Psychiatry.

Characterization of the central motor conduction time in a large cohort of spinocerebellar ataxia type 3 patients.

K. Xia, B. Tang, Hong Jiang, 2022, Parkinsonism & related disorders.

Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders

P. Jin, K. Xia, B. Tang, 2019, American journal of human genetics.

Identifying SYNE1 Ataxia With Novel Mutations in a Chinese Population

B. Tang, Hong Jiang, Xin Zhou, 2018, Front. Neurol..

Prediction of orthostatic hypotension in multiple system atrophy and Parkinson disease

K. Xia, B. Tang, Ji-feng Guo, 2016, Scientific Reports.

miRNA profiling in autism spectrum disorder in China

Hong Jiang, Z. Long, Chun-rong Wang, 2015, Genomics data.

miR‐25 alleviates polyQ‐mediated cytotoxicity by silencing ATXN3

Li Zhang, D. Chuang, K. Xia, 2014, FEBS letters.

Prediction of the Age at Onset of Spinocerebellar Ataxia Type 3 with Machine Learning

Zuping Zhang, K. Xia, Jinchen Li, 2020, Movement disorders : official journal of the Movement Disorder Society.

The APOE ε2 allele may decrease the age at onset in patients with spinocerebellar ataxia type 3 or Machado-Joseph disease from the Chinese Han population

K. Xia, B. Tang, Hong Jiang, 2014, Neurobiology of Aging.

Targeted Next-Generation Sequencing Revealed Novel Mutations in Chinese Ataxia Telangiectasia Patients: A Precision Medicine Perspective

K. Xia, B. Tang, Hong Jiang, 2015, PloS one.

Analysis of (CAG)n expansion in ATXN1, ATXN2 and ATXN3 in Chinese patients with multiple system atrophy

K. Xia, H. Peng, B. Tang, 2018, Scientific Reports.

Mutation spectrum of amyotrophic lateral sclerosis in Central South China

B. Tang, Ling Huang, Hong Jiang, 2021, Neurobiology of Aging.

Synaptic Loss in Spinocerebellar Ataxia Type 3 Revealed by SV2A Positron Emission Tomography

Yiyun Huang, M. Zhou, T. Ashizawa, 2023, Movement disorders : official journal of the Movement Disorder Society.

Diagnostic and prognostic performance of plasma neurofilament light chain in multiple system atrophy: a cross-sectional and longitudinal study

Jinchen Li, B. Tang, Hong Jiang, 2023, Journal of Neurology.

Hepatic encephalopathy coexists with acquired chronic hepatocerebral degeneration

X. Hou, F. Huang, T. Zhou, 2015, Neurosciences.

Blood Neurofilament Light Chain in Genetic Ataxia: A Meta‐Analysis

T. Klockgether, T. Ashizawa, K. Xia, 2021, Movement disorders : official journal of the Movement Disorder Society.

Mitochondrial genome variations are associated with amyotrophic lateral sclerosis in patients from mainland China

Mingyu Liang, B. Tang, Hong Jiang, 2021, Journal of Neurology.