Publications by authors named "Fanxi Xu"

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Genetic profiles of multiple system atrophy revealed by exome sequencing, long-read sequencing and spinocerebellar ataxia repeat expansion analysis.
Xu-Ying Li, Hong Lai, Xian Li, Fanxi Xu, Yang Song, Zhiheng Xu

Eur J Neurol· December 2024

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Pyruvate is modified by tea/coffee metabolites and reversely correlated with multiple system atrophy and Parkinson's disease.
Xu-Ying Li, Teng Xue, Hong Lai, Jing Dai, Fangda Peng, Fanxi Xu, Zhiheng Xu

Heliyon· March 2024

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Multidisciplinary molecular consultation increases the diagnosis of pediatric epileptic encephalopathy and neurodevelopmental disorders.
Liping Zhang, Xu-Ying Li, Fanxi Xu, Lehong Gao, Zhanjun Wang

Mol Genet Genomic Med· November 2023

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Applications of Machine Learning to Diagnosis of Parkinson's Disease.
Hong Lai, Xu-Ying Li, Fanxi Xu, Junge Zhu, Xian Li

Brain Sci· November 2023

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ACO2 deficiency increases vulnerability to Parkinson's disease via dysregulating mitochondrial function and histone acetylation-mediated transcription of autophagy genes.
Junge Zhu, Fanxi Xu, Hong Lai, Huiyao Yuan, Xu-Ying Li

Commun Biol· November 2023

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Clinical and Preclinical Neuroimaging Changes in Spinocerebellar Ataxia Type 12: A Study of Three Chinese Pedigrees.
Tingyan Yao, Hongwen Qiao, Junyan Sun, Xuying Li, Yang Song, Fanxi Xu

Eur Neurol· November 2022

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Identification of TARDBP Gly298Ser as a founder mutation for amyotrophic lateral sclerosis in Southern China.
Fanxi Xu, Sen Huang, Xu-Ying Li, Jianing Lin, Xiuli Feng, Yanming Xu, Xusheng Huang

BMC Med Genomics· August 2022

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Development and Validation of a Predictive Nomogram for Possible REM Sleep Behavior Disorders.
Hong Lai, Xu-Ying Li, Junya Hu, Wei Li, Fanxi Xu, Junjie Xu

Front Neurol· June 2022

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A novel loss-of-function compound heterozygous mutation of MYORG causes idiopathic basal ganglia calcification 7.
Junge Zhu, Fanxi Xu, Chaodong Wang, Xu-Ying Li, Guoguang Zhao

Parkinsonism Relat Disord· April 2022

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Genetic, clinical and neuroimaging profiles of sporadic and autosomal recessive hereditary spastic paraplegia cases in Chinese.
Yue Dong, Xu-Ying Li, Xian-Ling Wang, Fanxi Xu, Zhan-Jun Wang

Neurosci Lett· September 2021

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A novel FBXO7-R345P mutation in a Chinese family with autosomal recessive parkinsonian-pyramidal syndrome.
Zhanjun Wang, Yang Song, Wenjia Zhu, Xianling Wang, Xuying Li, Fanxi Xu

Parkinsonism Relat Disord· July 2021

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Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese families.
Zhanjun Wang, Yang Song, Xianling Wang, Xuying Li, Fanxi Xu

Neurosci Lett· May 2021

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Efficacy and Tolerability of Intravenous Immunoglobulin and Subcutaneous Immunoglobulin in Neurologic Diseases.
Yun Chen, Chunyu Wang, Fanxi Xu, Fengyu Ming, Hainan Zhang

Clin Ther· October 2019

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