Lee, Yi-Chung
National Yang Ming Chiao Tung University · Taipei Veterans General Hospital
6 papers on CoChatORCID 0000-0003-0102-164X
Most cited papers
- Verified
Incidental findings on brain magnetic resonance imaging: systematic review and meta-analysis
Morris, Z., Whiteley, W. N., Longstreth, W. T., Weber, F., Lee, Y.-C., Tsushima, Y., Alphs, H., Ladd, S. C., Warlow, C., Wardlaw, J. M., et al. (2009) · BMJ
Radiology practices and educationAdvanced MRI Techniques and Applications
Cited by 792
- Verified
Safety and efficacy of rozanolixizumab in patients with generalised myasthenia gravis (MycarinG): a randomised, double-blind, placebo-controlled, adaptive phase 3 study
Bril, V., Drużdż, A., Grosskreutz, J., Habib, A. A., Mantegazza, R., Sacconi, S., Utsugisawa, K., Vissing, J., Vu, T., Boehnlein, M., et al. (2023) · The Lancet Neurology
Myasthenia Gravis and ThymomaPeripheral Neuropathies and Disorders
Cited by 295
- Verified
Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study
Adams, D., Polydefkis, M., González-Duarte, A., Wixner, J., Kristen, A. V., Schmidt, H. H., Berk, J. L., Losada López, I. A., Dispenzieri, A., Quan, D., et al. (2021) · The Lancet Neurology
Amyloidosis: Diagnosis, Treatment, OutcomesAlzheimer's disease research and treatments
Cited by 158
- Verified
Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic Profiles
Liao, Y.-C., Hsiao, C.-T., Fuh, J.-L., Chern, C.-M., Lee, W.-J., Guo, Y.-C., Wang, S.-J., Lee, I.-H., Liu, Y.-T., Wang, Y.-F., et al. (2015) · PLOS ONE
Cerebrovascular and genetic disordersGenetic Neurodegenerative Diseases
Cited by 123
- Verified
Disease Severity Staging System for NOTCH3 -Associated Small Vessel Disease, Including CADASIL
Gravesteijn, G., Rutten, J. W., Cerfontaine, M. N., Hack, R. J., Liao, Y.-C., Jolly, A. A., Guey, S., Hsu, S.-L., Park, J.-Y., Yuan, Y., et al. (2025) · JAMA Neurology
Cerebrovascular and genetic disordersGenetic Neurodegenerative Diseases
Cited by 25
- Verified
Investigating ABCD1 mutations in a Taiwanese cohort with hereditary spastic paraplegia phenotype
Hsu, S.-L., Chen, Y.-H., Chou, C.-T., Chou, Y.-T., Tsai, Y.-S., Hsiao, C.-T., Liao, Y.-C., & Lee, Y.-C. (2021) · Parkinsonism & Related Disorders
Hereditary Neurological DisordersMetabolism and Genetic Disorders
Cited by 3
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