Works by Tang, Bei-Sha

Results: 61

Identification of the Largest SCA36 Pedigree in Asia: with Multimodel Neuroimaging Evaluation for the First Time.

Published in:

Cerebellum, 2022, v. 21, n. 3, p. 358, doi. 10.1007/s12311-021-01304-0

By:

Xie, Yue;
Chen, Zhao;
Long, Zhe;
Chen, Rui-Ting;
Jiang, Yi-Zheng;
Liu, Ming-Jie;
Peng, Lin-Liu;
Peng, Hui-Rong;
Wan, Na;
Zou, Guangdong;
Wang, Chun-Rong;
Shi, Yu-Ting;
Zhou, Gao-Feng;
Liao, Wei-Hua;
Qiu, Rong;
Hu, Zheng-Mao;
Xia, Kun;
Tang, Bei-Sha;
Jiang, Hong

Publication type:

Article

Lithium Chloride Alleviates Neurodegeneration Partly by Inhibiting Activity of GSK3β in a SCA3 Drosophila Model.

Published in:

Cerebellum, 2013, v. 12, n. 6, p. 892, doi. 10.1007/s12311-013-0498-3

By:

Jia, Dan-Dan;
Zhang, Li;
Chen, Zhao;
Wang, Chun-Rong;
Huang, Feng-Zhen;
Duan, Ran-Hui;
Xia, Kun;
Tang, Bei-Sha;
Jiang, Hong

Publication type:

Article

Constructing Prediction Models for Freezing of Gait by Nomogram and Machine Learning: A Longitudinal Study.

Published in:

Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.684044

By:

Xu, Kun;
Zhou, Xiao-xia;
He, Run-cheng;
Zhou, Zhou;
Liu, Zhen-hua;
Xu, Qian;
Sun, Qi-ying;
Yan, Xin-xiang;
Wu, Xin-yin;
Guo, Ji-feng;
Tang, Bei-sha

Publication type:

Article

Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients.

Published in:

2018

By:

Tian, Wo‐Tu;
Huang, Xiao‐Jun;
Mao, Xiao;
Liu, Qing;
Liu, Xiao‐Li;
Zeng, Sheng;
Guo, Xia‐Nan;
Shen, Jun‐Yi;
Xu, Yang‐Qi;
Tang, Hui‐Dong;
Yin, Xiao‐Meng;
Zhang, Mei;
Tang, Wei‐Guo;
Liu, Xiao‐Rong;
Tang, Bei‐Sha;
Chen, Sheng‐Di;
Cao, Li;
Tian, Wo-Tu;
Huang, Xiao-Jun;
Liu, Xiao-Li

Publication type:

journal article

Increase of the plasma α-synuclein levels in patients with multiple system atrophy.

Published in:

Movement Disorders, 2014, v. 29, n. 3, p. 375, doi. 10.1002/mds.25688

By:

Sun, Zhan‐Fang;
Xiang, Xiao‐Shuang;
Chen, Zhao;
Zhang, Li;
Tang, Bei‐Sha;
Xia, Kun;
Jiang, Hong

Publication type:

Article

PRRT2 gene mutations in familial and sporadic paroxysmal kinesigenic dyskinesia cases.

Published in:

Movement Disorders, 2013, v. 28, n. 9, p. 1313, doi. 10.1002/mds.25370

By:

Shi, Chang‐he;
Sun, Shi‐lei;
Wang, Jun‐ling;
Liu, Ai‐qin;
Miao, Wang;
Avinash, Chandra;
Mao, Xiao;
Tang, Bei‐sha;
Xu, Yu‐ming

Publication type:

Article

Glucocerebrosidase Gene L444P mutation is a risk factor for Parkinson's disease in Chinese population.

Published in:

Movement Disorders, 2010, v. 25, n. 8, p. 1005, doi. 10.1002/mds.23009

By:

Sun, Qi-Ying;
Guo, Ji-Feng;
Wang, Lei;
Yu, Ren-He;
Zuo, Xing;
Yao, Ling-Yan;
Pan, Qian;
Xia, Kun;
Tang, Bei-Sha

Publication type:

Article

Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: Genetic, clinical, and positron emission tomography findings.

Published in:

Movement Disorders, 2009, v. 24, n. 13, p. 2007, doi. 10.1002/mds.22727

By:

Wang, Jun-Ling;
Xiao, Bin;
Cui, Xiang-Xiang;
Guo, Ji-Feng;
Lei, Li-Fang;
Song, Xing-Wang;
Shen, Lu;
Jiang, Hong;
Yan, Xin-Xiang;
Pan, Qian;
Long, Zhi-Gao;
Xia, Kun;
Tang, Bei-Sha

Publication type:

Article

Mutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset Parkinsonism.

Published in:

Movement Disorders, 2008, v. 23, n. 14, p. 2074, doi. 10.1002/mds.22156

By:

Guo, Ji-Feng;
Xiao, Bin;
Liao, Bing;
Zhang, Xue-Wei;
Nie, Li-Luo;
Zhang, Yu-Hu;
Shen, Lu;
Jiang, Hong;
Xia, Kun;
Pan, Qian;
Yan, Xin-Xiang;
Tang, Bei-Sha

Publication type:

Article

Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration.

Published in:

2005

By:

Zhang, Yu-hu;
Tang, Bei-sha;
Zhao, Ai-ling;
Xia, Kun;
Long, Zhi-gao;
Guo, Ji-feng;
Westaway, Shawn K.;
Hayflick, Susan J.

Publication type:

journal article

The contribution of GIGYF2 to Parkinson's disease: a meta-analysis.

Published in:

2015

By:

Zhang, Yuan;
Sun, Qi-ying;
Yu, Ren-he;
Guo, Ji-feng;
Tang, Bei-sha;
Yan, Xin-xiang

Publication type:

journal article

A rare Von Hippel-Lindau disease that mimics acute myelitis: case report and review of the literature.

Published in:

Neurological Sciences, 2011, v. 32, n. 2, p. 305, doi. 10.1007/s10072-010-0413-3

By:

Jiang, Hong;
Shi, Yu-ting;
Wang, Jun-ling;
Tang, Bei-sha;
Wang, Jun-yu;
Peng, Ze-feng;
Xiao, De-sheng

Publication type:

Article

Clinical features and [11C]-CFT PET analysis of PARK2, PARK6, PARK7-linked autosomal recessive early onset Parkinsonism.

Published in:

2011

By:

Guo JF;
Wang L;
He D;
Yang QH;
Duan ZX;
Zhang XW;
Nie LL;
Yan XX;
Tang BS;
Guo, Ji-feng;
Wang, Lei;
He, Dan;
Yang, Qiao-hong Ou;
Duan, Zhong-xiang;
Zhang, Xue-wei;
Nie, Li-luo;
Yan, Xin-xiang;
Tang, Bei-sha

Publication type:

journal article

Clinical features and [C]-CFT PET analysis of PARK2, PARK6, PARK7-linked autosomal recessive early onset Parkinsonism.

Published in:

Neurological Sciences, 2011, v. 32, n. 1, p. 35, doi. 10.1007/s10072-010-0360-z

By:

Guo, Ji-feng;
Wang, Lei;
He, Dan;
Yang, Qiao-hong;
Duan, Zhong-xiang;
Zhang, Xue-wei;
Nie, Li-luo;
Yan, Xin-xiang;
Tang, Bei-sha

Publication type:

Article

Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment.

Published in:

Nature Genetics, 1998, v. 20, n. 4, p. 370, doi. 10.1038/3845

By:

Xia, Jia-hui;
Liu, Chun-yu;
Tang, Bei-sha;
Pan, Qian;
Huang, Lei;
Dai, He-ping;
Zhang, Bao-rong;
Xie, Wei;
Hu, Dong-xu;
Zheng, Duo;
Shi, Xiao-liu;
Wang, De-an;
Xia, Kun;
Yu, Kuan-ping;
Liao, Xiao-dong;
Feng, Yong;
Yang, Yi-feng;
Xiao, Jian-yun;
Xie, Ding-hua

Publication type:

Article

Advances on the genetic mechanism of amyotrophic lateral sclerosis.

Published in:

Chinese Journal of Contemporary Neurology & Neurosurgery, 2023, v. 23, n. 3, p. 264, doi. 10.3969/j.issn.1672-6731.2023.03.017

By:

ZHAO Qian-qian;
LI Wan-zhen;
TANG Bei-sha;
WANG Jun-ling

Publication type:

Article

Brain bank in neurology history and development.

Published in:

Chinese Journal of Contemporary Neurology & Neurosurgery, 2020, v. 20, n. 10, p. 914, doi. 10.3969/j.issn.1672-6731.2020.10.012

By:

CAO Ling-xiao;
HUANG Yue;
CAI Zhi-you;
CHAN Piu;
CHEN Sheng-di;
FAN Dong-sheng;
FANG Bo- yan;
GUO Yan-jun;
HAN Ying;
HUANG Hua-pin;
JI Wen-jun;
LI Hong-yan;
LIU Kun;
PEI Zhong;
PENG Dan-tao;
SHI Fu-dong;
SUI Yi;
TANG Bei-sha;
WANG Feng;
WANG Wen

Publication type:

Article

Progress in treatment of Charcot?Marie?Tooth disease.

Published in:

Chinese Journal of Contemporary Neurology & Neurosurgery, 2017, v. 17, n. 8, p. 566, doi. 10.3969/j.issn.1672-6731.2017.08.003

By:

ZHANG Ru-xu;
TANG Bei-sha

Publication type:

Article

Clinical standards and interpretation of gene sequence variants in human Mendelian disorders.

Published in:

Chinese Journal of Contemporary Neurology & Neurosurgery, 2017, v. 17, n. 7, p. 471, doi. 10.3969/j.issn.1672-6731.2017.07.001

By:

TANG Bei-sha;
ZENG Sheng;
LI Kai

Publication type:

Article

The Association Between Lysosomal Storage Disorder Genes and Parkinson's Disease: A Large Cohort Study in Chinese Mainland Population.

Published in:

Frontiers in Aging Neuroscience, 2021, v. 13, p. 1, doi. 10.3389/fnagi.2021.749109

By:

Zhao, Yu-wen;
Pan, Hong-xu;
Liu, Zhenhua;
Wang, Yige;
Zeng, Qian;
Fang, Zheng-huan;
Luo, Teng-fei;
Xu, Kun;
Wang, Zheng;
Zhou, Xun;
He, Runcheng;
Li, Bin;
Zhao, Guihu;
Xu, Qian;
Sun, Qi-ying;
Yan, Xin-xiang;
Tan, Jie-qiong;
Li, Jin-chen;
Guo, Ji-feng;
Tang, Bei-sha

Publication type:

Article

The Progress of Induced Pluripotent Stem Cells as Models of Parkinson’s Disease.

Published in:

Thrombosis, 2016, p. 1, doi. 10.1155/2016/4126214

By:

Kang, Ji-feng;
Tang, Bei-sha;
Guo, Ji-feng

Publication type:

Article

Spinocerebellar Ataxia Type 13 is an Uncommon SCA Subtype in the Chinese Han Population.

Published in:

International Journal of Neuroscience, 2013, v. 123, n. 7, p. 450, doi. 10.3109/00207454.2013.763254

By:

Peng, Lan;
Wang, Chunrong;
Chen, Zhao;
Wang, Jun-Ling;
Tang, Bei-Sha;
Jiang, Hong

Publication type:

Article

Autophagy and Its Comprehensive Impact on ALS.

Published in:

International Journal of Neuroscience, 2012, v. 122, n. 12, p. 695, doi. 10.3109/00207454.2012.714430

By:

Song, Cheng-yuan;
Guo, Ji-feng;
Liu, Yuan;
Tang, Bei-sha

Publication type:

Article

ASSOCIATION ANALYSIS OF SEROTONIN TRANSPORTER PROMOTER GENE POLYMORPHISM WITH ADHD AND RELATED SYMPTOMATOLOGY.

Published in:

International Journal of Neuroscience, 2005, v. 115, n. 8, p. 1183, doi. 10.1080/00207450590914545

By:

ZHAO, AI-LING;
SU, LIN-YAN;
ZHANG, YU-HU;
TANG, BEI-SHA;
LUO, XUE-RONG;
HUANG, CHUN-XIANG;
SU, QIAO-RONG

Publication type:

Article

Research advances on neurite outgrowth inhibitor B receptor.

Published in:

Journal of Cellular & Molecular Medicine, 2020, v. 24, n. 14, p. 7697, doi. 10.1111/jcmm.15391

By:

Zhang, Rui;
Tang, Bei‐sha;
Guo, Ji‐feng

Publication type:

Article

SPG46 and SPG56 are rare causes of hereditary spastic paraplegia in China.

Published in:

2016

By:

Yang, Yi-Jing;
Zhou, Zhi-Fan;
Liao, Xin-Xin;
Luo, Ying-Ying;
Zhan, Zi-Xiong;
Huang, Mu-Fang;
Zhou, Lu;
Tang, Bei-Sha;
Shen, Lu;
Du, Juan

Publication type:

Letter

Telomere Length and COVID-19 Outcomes: A Two-Sample Bidirectional Mendelian Randomization Study.

Published in:

Frontiers in Genetics, 2022, p. 1, doi. 10.3389/fgene.2022.805903

By:

Jiang, Li;
Tang, Bei-sha;
Guo, Ji-feng;
Li, Jin-chen

Publication type:

Article

Parkinson’s Disease and Cognitive Impairment.

Published in:

Parkinson's Disease (20420080), 2016, p. 1, doi. 10.1155/2016/6734678

By:

Yang, Yang;
Tang, Bei-sha;
Guo, Ji-feng

Publication type:

Article

The Progress of Induced Pluripotent Stem Cells as Models of Parkinson’s Disease.

Published in:

Stem Cells International, 2016, p. 1, doi. 10.1155/2016/4126214

By:

Kang, Ji-feng;
Tang, Bei-sha;
Guo, Ji-feng

Publication type:

Article

Associations between gut microbiota and Parkinson disease: A bidirectional Mendelian randomization analysis.

Published in:

European Journal of Neurology, 2023, v. 30, n. 11, p. 3471, doi. 10.1111/ene.15848

By:

Jiang, Li;
Li, Jin‐chen;
Tang, Bei‐sha;
Guo, Ji‐feng

Publication type:

Article

NRBF2 is a RAB7 effector required for autophagosome maturation and mediates the association of APP-CTFs with active form of RAB7 for degradation.

Published in:

Autophagy, 2021, v. 17, n. 5, p. 1112, doi. 10.1080/15548627.2020.1760623

By:

Cai, Cui-Zan;
Yang, Chuanbin;
Zhuang, Xu-Xu;
Yuan, Ning-Ning;
Wu, Ming-Yue;
Tan, Jie-Qiong;
Song, Ju-Xian;
Cheung, King-Ho;
Su, Huanxing;
Wang, Yi-Tao;
Tang, Bei-Sha;
Behrends, Christian;
Durairajan, Siva Sundara Kumar;
Yue, Zhenyu;
Li, Min;
Lu, Jia-Hong

Publication type:

Article

BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage.

Published in:

Oxidative Medicine & Cellular Longevity, 2017, p. 1, doi. 10.1155/2017/5094934

By:

Qin, Li-xia;
Tan, Jie-qiong;
Zhang, Hai-nan;
Rizwana, Kousar;
Lu, Jia-hong;
Tang, Jian-guang;
Jiang, Bo;
Shen, Xiang-min;
Guo, Ji-feng;
Tang, Bei-sha;
Tan, Li-ming;
Wang, Chun-yu

Publication type:

Article

Identification of a Locus for Disseminated Superficial Actinic Porokeratosis at Chromosome 12q23.2–24.1.

Published in:

Journal of Investigative Dermatology, 2000, v. 114, n. 6, p. 1071, doi. 10.1046/j.1523-1747.2000.00978.x

By:

Xia, Jia-Hui;
Yang, Yi-Feng;
Deng, Hao;
Tang, Bei-Sha;
Tang, Dong-Sheng;
He, Yun-Gui;
Xia, Kun;
Chen, Sheng-Xiang;
Li, Yi-Xiong;
Pan, Qian;
Long, Zhi-Gao;
Dai, He-Ping;
Liao, Xiao-Dong;
Xiao, Jian-Feng;
Liu, Zhi-Ran;
Lu, Chun-Ye;
Yu, Kuan-Ping;
Deng, Han-Xiang

Publication type:

Article

Two novel functional single nucleotide polymorphisms of ADRB3 are associated with type 2 diabetes in the Chinese population.

Published in:

2013

By:

Huang, Qiong;
Yang, Tian-Lun;
Tang, Bei-Sha;
Chen, Xiang;
Huang, Xi;
Luo, Xiang-Hang;
Zhu, Yuan-Shan;
Chen, Xiao-Ping;
Hu, Ping-Cheng;
Chen, Juan;
Wei, Wei;
Zhou, Hong-Hao;
Yin, Ji-Ye;
Liu, Zhao-Qian

Publication type:

Journal Article

Gluten ataxia of sporadic and hereditary cerebellar ataxia in patients from mainland China.

Published in:

2013

By:

Guan, Wen-Juan;
Liu, Xin-Jian;
Tang, Bei-Sha;
Liu, Yu-Tao;
Zhou, Ying;
Jiang, Hong;
Shen, Lu;
Xia, Kun;
Wang, Jun-Ling

Publication type:

journal article

TNFSF4 gene polymorphism rs3861950 but not rs3850641 is associated with the risk of cerebral infarction in a Chinese population.

Published in:

Journal of Thrombosis & Thrombolysis, 2013, v. 36, n. 3, p. 307, doi. 10.1007/s11239-012-0849-9

By:

Feng, Jie;
Liu, Yun-Hai;
Yang, Qi-Dong;
Zhu, Zan-Hua;
Xia, Kun;
Tan, Xing-Lin;
Xia, Jian;
Gu, Wen-Ping;
Zhou, Lin;
Xiao, Bo;
Tang, Bei-Sha;
Huang, Qing

Publication type:

Article

Effect of GBA Mutations on Phenotype of Parkinson’s Disease: A Study on Chinese Population and a Meta-Analysis.

Published in:

Parkinson's Disease (20420080), 2015, v. 2015, p. 1, doi. 10.1155/2015/916971

By:

Zhang, Yuan;
Sun, Qi-ying;
Zhao, Yu-wen;
Shu, Li;
Guo, Ji-feng;
Xu, Qian;
Yan, Xin-xiang;
Tang, Bei-sha

Publication type:

Article

Distribution of Transglutaminase 6 in the Central Nervous System of Adult Mice.

Published in:

Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2013, v. 296, n. 10, p. 1576, doi. 10.1002/ar.22741

By:

Liu, Yu‐Tao;
Tang, Bei‐Sha;
Lan, Wei;
Song, Ning‐Ning;
Huang, Ying;
Zhang, Lei;
Guan, Wen‐Juan;
Shi, Yu‐Ting;
Shen, Lu;
Jiang, Hong;
Guo, Ji‐Feng;
Xia, Kun;
Ding, Yu‐Qiang;
Wang, Jun‐Ling

Publication type:

Article

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

Published in:

Human Genetics, 2005, v. 116, n. 3, p. 222, doi. 10.1007/s00439-004-1218-3

By:

Tang, Bei-sha;
Zhao, Guo-hua;
Luo, Wei;
Xia, Kun;
Cai, Fang;
Pan, Qian;
Zhang, Ru-xu;
Zhang, Fu-feng;
Liu, Xiao-min;
Chen, Biao;
Zhang, Cheng;
Shen, Lu;
Jiang, Hong;
Long, Zhi-gao;
Dai, He-ping

Publication type:

Article

High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson's disease.

Published in:

NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00722-1

By:

Wang, Chaodong;
Liu, Hankui;
Li, Xu-Ying;
Ma, Jinghong;
Gu, Zhuqin;
Feng, Xiuli;
Xie, Shu;
Tang, Bei-Sha;
Chen, Shengdi;
Wang, Wei;
Wang, Jian;
Zhang, Jianguo;
Chan, Piu

Publication type:

Article

Influence of simvastatin on dopaminergic neurons of lipopolysaccharide–induced rat model of Parkinson's disease.

Published in:

Asian Pacific Journal of Tropical Medicine, 2015, v. 8, n. 1, p. 64, doi. 10.1016/S1995-7645(14)60189-9

By:

Wang, Tan;
Cao, Xue-Bin;
Chen, Xiao-Wu;
Huang, Pei-Pei;
Zhang, Tian;
Chen, Zhi-Bin;
Tang, Bei-Sha

Publication type:

Article

UQCRC1 variants in Parkinson's disease: a large cohort study in Chinese mainland population.

Published in:

2021

By:

Zhao, Yu-wen;
Pan, Hong-xu;
Wang, Chun-yu;
Zeng, Qian;
Wang, Yige;
Fang, Zheng-huan;
Huang, Juanjuan;
Li, Xiaosong;
Wang, Xiaoye;
Zhang, Xi;
Liu, Zhen-hua;
Sun, Qi-ying;
Xu, Qian;
Lei, Li-fang;
Yan, Xin-xiang;
Shen, Lu;
Jiang, Hong;
Tan, Jie-qiong;
Li, Jin-chen;
Tang, Bei-sha

Publication type:

journal article

Reply: Assessing the NOTCH2NLC GGC expansion in essential tremor patients from eastern China.

Published in:

2021

By:

Sun, Qi-Ying;
Guo, Ji-Feng;
Tang, Bei-Sha

Publication type:

Letter

Reply: Assessing the NOTCH2NLC GGC expansion in European patients with essential tremor.

Published in:

2020

By:

Sun, Qi-Ying;
Guo, Ji-Feng;
Tang, Bei-Sha

Publication type:

Letter

HCFC1 variants in the proteolysis domain are associated with X‐linked idiopathic partial epilepsy: Exploring the underlying mechanism.

Published in:

Clinical & Translational Medicine, 2023, v. 13, n. 6, p. 1, doi. 10.1002/ctm2.1289

By:

He, Na;
Guan, Bao‐Zhu;
Wang, Jie;
Liu, Han‐Kui;
Mao, Yong;
Liu, Zhi‐Gang;
Yin, Fei;
Peng, Jing;
Xiao, Bo;
Tang, Bei‐sha;
Zhou, Dong;
Huang, Guang;
Dai, Qi‐Lin;
Zeng, Ying;
Han, Hong;
Zhai, Qiong‐Xiang;
Li, Bin;
Tang, Bin;
Li, Wen‐Bin;
Song, Wang

Publication type:

Article

Identification of clinically actionable secondary genetic variants from whole‐genome sequencing in a large‐scale Chinese population.

Published in:

Clinical & Translational Medicine, 2022, v. 12, n. 5, p. 1, doi. 10.1002/ctm2.866

By:

Cong, Pei‐Kuan;
Khederzadeh, Saber;
Yuan, Cheng‐Da;
Ma, Rui‐Jie;
Zhang, Yi‐Yao;
Liu, Jun‐Quan;
Yu, Shi‐Hui;
Xu, Lin;
Gao, Jian‐Hua;
Pan, Hong‐Xu;
Li, Jin‐Chen;
Xie, Shu‐Yang;
Liu, Ke‐Qi;
Tang, Bei‐Sha;
Zheng, Hou‐Feng

Publication type:

Article

Autonomic ganglionic injection of α-synuclein fibrils as a model of pure autonomic failure α-synucleinopathy.

Published in:

Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-019-14189-9

By:

Wang, Xue-Jing;
Ma, Ming-Ming;
Zhou, Le-Bo;
Jiang, Xiao-Yi;
Hao, Miao-Miao;
Teng, Robert K. F.;
Wu, Erxi;
Tang, Bei-Sha;
Li, Jia-Yi;
Teng, Jun-Fang;
Ding, Xue-Bing

Publication type:

Article

Genetic Identification Is Critical for the Diagnosis of Parkinsonism: A Chinese Pedigree with Early Onset of Parkinsonism.

Published in:

PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0136245

By:

Yang, Yang;
Tang, Bei-sha;
Weng, Ling;
Li, Nan;
Shen, Lu;
Wang, Jian;
Zuo, Chuan-tao;
Yan, Xin-xiang;
Xia, Kun;
Guo, Ji-feng

Publication type:

Article

Genetic Diagnosis of Two Dopa-Responsive Dystonia Families by Exome Sequencing.

Published in:

PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0106388

By:

Sun, Zhan-fang;
Zhang, Yu-han;
Guo, Ji-feng;
Sun, Qi-ying;
Mei, Jun-pu;
Zhou, Han-lin;
Guan, Li-ping;
Tian, Jin-yong;
Hu, Zheng-mao;
Li, Jia-da;
Xia, Kun;
Yan, Xin-xiang;
Tang, Bei-sha

Publication type:

Article

Analysis of EIF4G1 in ethnic Chinese.

Published in:

2013

By:

Li, Kai;
Tang, Bei-Sha;
Guo, Ji-Feng;
Lou, Ming-Xing;
Lv, Zhan-Yun;
Liu, Zhen-Hua;
Tian, Yun;
Song, Cheng-Yuan;
Xia, Kun;
Yan, Xin-Xiang

Publication type:

journal article