Yi-Jun Chen

发表

Cross sign T2 hyperintensities in atrophic spinal cord of hereditary spastic paraplegia type 5

Y. Liu, Wanjin Chen, Ning Wang, 2020 .

Novel ATP13A2 and PINK1 variants identified in Chinese patients with Parkinson’s disease by whole-exome sequencing

Yi-Jun Chen, Hui Chen, Qing-Qing Tao, 2020, Neuroscience Letters.

Functional study and pathogenicity classification of PRRT2 missense variants in PRRT2‐related disorders

Hong-Fu Li, Hai-Lin Dong, Yi-Jun Chen, 2019, CNS neuroscience & therapeutics.

Clinical Characterization and Founder Effect Analysis in Chinese Patients with Phospholipase A2-Associated Neurodegeneration

Hong-Fu Li, Yi-Jun Chen, Hao-Ling Cheng, 2022, Brain sciences.

Novel PLA2G6 mutations and clinical heterogeneity in Chinese cases with phospholipase A2-associated neurodegeneration.

W. Ni, Hong-Fu Li, Hai-Lin Dong, 2018, Parkinsonism & related disorders.

Chinese patients with adrenoleukodystrophy and Zellweger spectrum disorder presenting with hereditary spastic paraplegia.

Wanjin Chen, Ning Wang, Zaiqiang Zhang, 2019, Parkinsonism & related disorders.

Stop-gain mutations in UBAP1 cause pure autosomal-dominant spastic paraplegia.

Z. Xiong, Ning Wang, Hongjie Yu, 2019, Brain : a journal of neurology.

Novel Compound Missense and Intronic Splicing Mutation in ALDH18A1 Causes Autosomal Recessive Spastic Paraplegia

Ning Wang, Zaiqiang Zhang, Zhe Zhao, 2021, Frontiers in Neurology.

Genetic and Clinical Profile of Chinese Patients with Autosomal Dominant Spastic Paraplegia

Ning Wang, Xiang Lin, Yi-Jun Chen, 2019, Molecular Diagnosis & Therapy.

Bidirectional Connections between Depression and Ataxia Severity in Spinocerebellar Ataxia Type 3 Patients

Min-ting Lin, Ning Wang, Shi-Rui Gan, 2018, European Neurology.

Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia

Ning Wang, Xiang Lin, Yi-Jun Chen, 2020, Annals of clinical and translational neurology.

Association Between Body Mass Index and Disease Severity in Chinese Spinocerebellar Ataxia Type 3 Patients

Min-ting Lin, Ning Wang, Shi-Rui Gan, 2018, The Cerebellum.

Homozygote of spinocerebellar Ataxia type 3 correlating with severe phenotype based on analyses of clinical features

Min-ting Lin, Ning Wang, Shi-Rui Gan, 2018, Journal of the Neurological Sciences.

Alu Retrotransposition Event in SPAST Gene as a Novel Cause of Hereditary Spastic Paraplegia

Yusen Qiu, Xiang Lin, Yi-Jun Chen, 2023, Movement disorders : official journal of the Movement Disorder Society.

Chinese patients with hereditary spastic paraplegias (HSPs): a protocol for a hospital-based cohort study

Y. Liu, Ning Wang, Yi Lin, 2022, BMJ Open.

Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization

Yi-Chung Lee, Yusen Qiu, Xiang Lin, 2023, Movement disorders : official journal of the Movement Disorder Society.