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Scientific Reports|May 19, 2023
Baseline P2Y12 reactivity, kidney function, and CYP2C19 genotype determine clopidogrel responsiveness in acute strokeYi-Chung Lee, Yi-Chu Liao, Chun-Jen Lin, et al.International Psychogeriatrics|September 28, 2005
Family members favor disclosing the diagnosis of Alzheimer's diseaseKer-Neng Lin, Yi-Chu Liao, Pei-Ning Wang, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|June 15, 2013
Which nerve conduction parameters can predict spontaneous electromyographic activity in carpal tunnel syndrome?Chia-Wei Chang, Wei-Ju Lee, Yi-Chu Liao, et al.Neurobiology of Aging|September 20, 2020
Mitochondrial DNA m.3243A>G mutation rarely causes CADASIL-like phenotypeNai-Yi Liao, Kwong-Kum Liao, Yi-Chu Liao, et al.Plos One|September 16, 2014
Initial medication in patients of newly diagnosed Parkinson's disease in TaiwanYi-Jen Guo, Yi-Chu Liao, Ching-Heng Lin, et al.Journal of the Chinese Medical Association : JCMA|May 30, 2025
Incidence and characteristics of Guillain-Barré syndrome in Taiwan before and during the COVID-19 pandemic: A 12-year single-center experienceYu-Hsin Chen, Kuan-Lin Lai, Yi-Chung Lee, et al.Journal of Clinical Neurology (Seoul, Korea)|January 6, 2023
Update on the Epidemiology, Pathogenesis, and Biomarkers of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and LeukoencephalopathyYumi Yamamoto, Yi-Chu Liao, Yi-Chung Lee, et al.Acta Neurologica Taiwanica|March 10, 2022
Transient Postictal Hyperglycemia as a Diagnostic Clue of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like EpisodesNai-Yi Liao, Liang-Yu Lin, Chien Chen, et al.Scientific Reports|November 14, 2020
Mutational analysis in familial Alzheimer's disease of Han Chinese in Taiwan with a predominant mutation PSEN1 p.Met146IleYung-Shuan Lin, Chih-Ya Cheng, Yi-Chu Liao, et al.Journal of the Chinese Medical Association : JCMA|January 4, 2023
Reduced-penetrance Huntington's disease-causing alleles with 39 CAG trinucleotide repeats could be a genetic factor of amyotrophic lateral sclerosisKang-Yang Jih, Kuan-Lin Lai, Kon-Ping Lin, et al.Pageof 19