Challenge and strategy in the diagnosis and treatment of Wilson's disease by Yue ZHANG, Zhi⁃ying WU

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Huntington Disease in Asia by Miao Xu, Zhi-Ying Wu

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Amyotrophic Lateral Sclerosis: Precise Diagnosis and Individualized Treatment by Qing-Qing Tao, Zhi-Ying Wu

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Phenotypic variance in monozygotic twins with SCA3 by Hua Zhao, Lu Yang, Yi Dong, Zhi‐Ying Wu

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Genotype-phenotype correlation in Chinese patients with spinal and bulbar muscular atrophy. by Wang Ni, Sheng Chen, Kai Qiao, Ning Wang, Zhi-Ying Wu

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A De novo Mutation in Dystrophin Causing Muscular Dystrophy in a Female Patient by Hao Yu, Yu-Chao Chen, Gong-Lu Liu, Zhi-Ying Wu

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A Novel Missense Mutation in Peripheral Myelin Protein-22 Causes Charcot-Marie-Tooth Disease by Li-Xi Li, Hai-Lin Dong, Bao-Guo Xiao, Zhi-Ying Wu

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Population genetics and new insight into range of CAG repeats of spinocerebellar ataxia type 3 in the Han Chinese population. by Shi-Rui Gan, Wang Ni, Yi Dong, Ning Wang, Zhi-Ying Wu

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Clinical feature difference between juvenile amyotrophic lateral sclerosis with SPTLC1 and FUS mutations by Peishan Wang, Qiao Wei, Hongfu Li, Zhi-Ying Wu, Rongman Jia, Xiuyuan Hao

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Biallelic SORD pathogenic variants cause Chinese patients with distal hereditary motor neuropathy by Hai-Lin Dong, Jia-Qi Li, Gong-Lu Liu, Hao Yu, Zhi-Ying Wu

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Acute-Onset Visual Impairment in Wilson's Disease: A Case Report and Literature Review by Zi-Wei Zheng, Meng-Hui Xu, Chuan-Bin Sun, Zhi-Ying Wu, Yi Dong

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The role of apolipoprotein E as a risk factor for an earlier age at onset for Machado-Joseph disease is doubtful. by Qi Zhou, Wang Ni, Yi Dong, Ning Wang, Shi-Rui Gan, Zhi-Ying Wu

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Genotype-phenotype correlation and founder effect analysis in southeast Chinese patients with sialidosis type I by Yi-Chu Du, Ling-Han Ma, Quan-Fu Li, Yin Ma, Yi Dong, Zhi-Ying Wu

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Clinical and genetic characteristics of Chinese patients with cerebrotendinous xanthomatosis by Qing-Qing Tao, Yun Zhang, Hui-Xia Lin, Hai-Lin Dong, Wang Ni, Zhi-Ying Wu

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Clinical characterization and founder effect analysis in Chinese amyotrophic lateral sclerosis patients with SOD1 common variants by Pei-Shan Wang, Xin-Xia Yang, Qiao Wei, Yong-Ting Lv, Zhi-Ying Wu, Hong-Fu Li

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Variants of Interferon Regulatory Factor 5 are Associated with Neither Neuromyelitis Optica Nor Multiple Sclerosis in the Southeastern Han Chinese Population by Qi-Bing Liu, Lei Wu, Gui-Xian Zhao, Ping-Ping Cai, Zhen-Xin Li, Zhi-Ying Wu

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A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia by Qiao Wei, Pei‐Shan Wang, Hai‐Lin Dong, Wen‐Jiao Luo, Zhi‐Ying Wu, Hong‐Fu Li

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Clinical Characterization and Founder Effect Analysis in Chinese Patients with Phospholipase A2-Associated Neurodegeneration by Hao-Ling Cheng, Yi-Jun Chen, Yan-Yan Xue, Zhi-Ying Wu, Hong-Fu Li, Ning Wang

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Clinical features and genetic characteristics of homozygous spinocerebellar ataxia type 3 by Quan-Fu Li, Hao‐Ling Cheng, Lu Yang, Yin Ma, Jing‐Jing Zhao, Yi Dong, Zhi‐Ying Wu

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Optimal Combinations of AT(N) Biomarkers to Determine Longitudinal Cognition in the Alzheimer's Disease by Rong-Rong Lin, Yan-Yan Xue, Xiao-Yan Li, Yi-He Chen, Qing-Qing Tao, Zhi-Ying Wu

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