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Acta Neurologica Taiwanica|June 4, 2015
[Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)]Yun-Chung Chen, Cheng-Tsung Hsiao, Bing-Wen Soong, et al.Journal of the Neurological Sciences|December 4, 2014
C9ORF72 repeat expansion is not a significant cause of late onset cerebellar ataxia syndromeCheng-Tsung Hsiao, Pei-Chien Tsai, Yi-Chu Liao, et al.Acta Neurologica Taiwanica|October 4, 2024
Recent Advance in Disease Modifying Therapies for Spinal Muscular AtrophyLi-Kai Tsai, Chen-Hung Ting, Yo-Tsen Liu, et al.Journal of the Chinese Medical Association : JCMA|May 12, 2015
Acute simultaneous multiple lacunar infarcts as the initial presentation of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyCheng-Tsung Hsiao, Yun-Chung Chen, Yo-Tsen Liu, et al.Parkinsonism & Related Disorders|October 13, 2025
The genetic landscape of spinocerebellar ataxias in Taiwan: Insights from 876 genetically confirmed casesShih-Chun Lan, Cheng-Tsung Hsiao, Kang-Yang Jih, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|June 13, 2023
Identification of m.3243A>G mitochondrial DNA mutation in patients with cerebellar ataxiaNai-Yi Liao, Kuan-Lin Lai, Yi-Chu Liao, et al.Parkinsonism & Related Disorders|August 19, 2019
Investigating PUM1 mutations in a Taiwanese cohort with cerebellar ataxiaKuan-Lin Lai, Yi-Chu Liao, Pei-Chien Tsai, et al.Acta Neurologica Taiwanica|June 16, 2025
Intrafamilial Phenotypic Variation in Taiwanese Patients with Hereditary Spastic Paraplegia and Charcot-Marie-Tooth Disease Due to KIF5A Mutations: A Cross-Sectional Observational StudyPo-Yu Lin, Cheng-Tsung Hsiao, Han-Wei Huang, et al.Plos One|February 9, 2018
Correction: Mutational analysis of ITPR1 in a Taiwanese cohort with cerebellar ataxiasCheng-Tsung Hsiao, Yo-Tsen Liu, Yi-Chu Liao, et al.Plos One|November 30, 2017
Mutational analysis of ITPR1 in a Taiwanese cohort with cerebellar ataxiasCheng-Tsung Hsiao, Yo-Tsen Liu, Yi-Chu Liao, et al.Pageof 4