Yu-Shuen Tsai

发表

Hand‐onset weakness is a common feature of ALS patients with a NEK1 loss‐of‐function variant

P. Tsai, Yi-Chung Lee, Y. Liao, 2020, Annals of clinical and translational neurology.

Investigating ABCD1 mutations in a Taiwanese cohort with hereditary spastic paraplegia phenotype.

Yi-Chung Lee, Y. Liao, Yu-Shuen Tsai, 2021, Parkinsonism & related disorders.

Investigating KIF1A mutations in a Taiwanese cohort with hereditary spastic paraplegia.

Yi-Chung Lee, K. Yu, Y. Liao, 2022, Parkinsonism & related disorders.

Clinical and genetic characterization of NEFL-related neuropathy in Taiwan.

Yi-Chung Lee, Y. Liao, K. Lai, 2022, Journal of the Formosan Medical Association = Taiwan yi zhi.

Clinical and genetic characterization of hereditary spastic paraplegia type 3A in Taiwan.

Yi-Chung Lee, K. Yu, Yung-Yee Chang, 2021, Parkinsonism & related disorders.

A novel TFG mutation causes Charcot-Marie-Tooth disease type 2 and impairs TFG function

P. Tsai, Yi-Chung Lee, Yen‐Hua Huang, 2014, Neurology.

Lymphoid Enhancer Factor 1 Contributes to Hepatocellular Carcinoma Progression Through Transcriptional Regulation of Epithelial‐Mesenchymal Transition Regulators and Stemness Genes

Yen‐Hua Huang, G. Chau, Y. Yeh, 2018, Hepatology communications.

Intracerebral Hemorrhage in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: Prevalence, Clinical and Neuroimaging Features and Risk Factors.

Yi-Chung Lee, Yen-Feng Wang, Y. Liao, 2021, Stroke.

A PIAS1 Protective Variant S510G Delays polyQ Disease Onset by Modifying Protein Homeostasis

Yi-Chung Lee, H. Shih, Y. Chern, 2021, Movement disorders : official journal of the Movement Disorder Society.

Clinical and genetic characterization of adult‐onset leukoencephalopathy caused by CSF1R mutations

P. Tsai, Yi-Chung Lee, Pei-Ning Wang, 2021, Annals of clinical and translational neurology.

Mutation spectrum of Charcot‐Marie‐Tooth disease among the Han Chinese in Taiwan

Yi-Chung Lee, Y. Liao, Yuh-Cherng Guo, 2019, Annals of clinical and translational neurology.

Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia

P. Tsai, Yi-Chung Lee, Y. Liao, 2017, Journal of the Neurological Sciences.

Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia

P. Tsai, Yi-Chung Lee, K. Yu, 2023, Annals of clinical and translational neurology.

Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5

Yi-Chung Lee, Y. Liao, B. Soong, 2020, Annals of clinical and translational neurology.

Clinical and Genetic Characterization of Autosomal Recessive Spinocerebellar Ataxia Type 16 (SCAR16) in Taiwan

Yi-Chung Lee, Y. Liao, B. Soong, 2020, The Cerebellum.

Clinical and Genetic Characterization of Autosomal Recessive Spinocerebellar Ataxia Type 16 (SCAR16) in Taiwan

Yi-Chung Lee, Y. Liao, B. Soong, 2020, The Cerebellum.

A novel DNAJB6 mutation causes dominantly inherited distal‐onset myopathy and compromises DNAJB6 function

P. Tsai, Y. Liao, B. Soong, 2017, Clinical genetics.

Biallelic DDHD2 mutations in patients with adult‐onset complex hereditary spastic paraplegia

Yi-Chung Lee, K. Yu, Y. Liao, 2023, Annals of clinical and translational neurology.

Investigating ZFYVE26 mutations in a Taiwanese cohort with hereditary spastic paraplegia.

Yi-Chung Lee, Y. Liao, J. Fuh, 2021, Journal of the Formosan Medical Association = Taiwan yi zhi.

Expanding the phenotype of AFG3L2 mutations: Late-onset autosomal recessive spinocerebellar ataxia

Yi-Chung Lee, Y. Liao, J. Fuh, 2021, Journal of Neurological Sciences.

Reply to: “Low Frequency of p.S510G in PIAS1 Challenges Its Relevance for Modifying Repeat Expansion Disorders”

Yi-Chung Lee, Y. Chern, Tzu-Hao Cheng, 2022, Movement disorders : official journal of the Movement Disorder Society.

Disruption of the PAR3/INSC/LGN complex causes microtubule instability and peripheral neuropathy

Yi-Chung Lee, Chih-Chiang Chan, M. Kennerson, 2023, medRxiv.

Rapid progressive ALS in a patient with a DNAJC7 loss-of-function mutation

P. Tsai, Yi-Chung Lee, Y. Liao, 2020, Neurology: Genetics.

Characterization of a novel TFG variant causing autosomal recessive pure hereditary spastic paraplegia

Yi-Chung Lee, Yu-Shuen Tsai, C. Hsiao, 2024, Annals of clinical and translational neurology.