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Yi-Chung Lee
Yi-Chung Lee
Taipei Veterans General Hospital and National Yang Ming Chiao Tung Univeristy
在 vghtpe.gov.tw 的电子邮件经过验证
标题
引用次数
引用次数
年份
Incidental findings on brain magnetic resonance imaging: systematic review and meta-analysis
Z Morris, WN Whiteley, WT Longstreth, F Weber, YC Lee, Y Tsushima, ...
Bmj 339, 2009
8562009
Mutations in KCND3 cause spinocerebellar ataxia type 22
YC Lee, A Durr, K Majczenko, YH Huang, YC Liu, CC Lien, PC Tsai, ...
Annals of neurology 72 (6), 859-869, 2012
1802012
Cutoff scores of the cognitive abilities screening instrument, Chinese version in screening of dementia
KN Lin, PN Wang, CY Liu, WT Chen, YC Lee, HC Liu
Dementia and geriatric cognitive disorders 14 (4), 176-182, 2002
1702002
A Recurrent loss‐of‐function alanyl‐tRNA synthetase (AARS ) mutation in patients with charcot‐marie‐tooth disease type 2N (CMT2N)
HM McLaughlin, R Sakaguchi, W Giblin, ...
Human mutation 33 (1), 244-253, 2012
1312012
Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study
D Adams, M Polydefkis, A González-Duarte, J Wixner, AV Kristen, ...
The Lancet Neurology 20 (1), 49-59, 2021
1292021
Comparison of sensitivity of transcarpal median motor conduction velocity and conventional conduction techniques in electrodiagnosis of carpal tunnel syndrome
MH Chang, LH Liu, YC Lee, SJ Wei, HL Chiang, PF Hsieh
Clinical neurophysiology 117 (5), 984-991, 2006
1292006
ATXN2 trinucleotide repeat length correlates with risk of ALS
W Sproviero, A Shatunov, D Stahl, M Shoai, W van Rheenen, AR Jones, ...
Neurobiology of aging 51, 178. e1-178. e9, 2017
1222017
The mutational spectrum in a cohort of Charcot-Marie-Tooth disease type 2 among the Han Chinese in Taiwan
KP Lin, BW Soong, CC Yang, LW Huang, MH Chang, IH Lee, A Antonellis, ...
PLoS One 6 (12), e29393, 2011
1142011
Characterization of CADASIL among the Han Chinese in Taiwan: distinct genotypic and phenotypic profiles
YC Liao, CT Hsiao, JL Fuh, CM Chern, WJ Lee, YC Guo, SJ Wang, IH Lee, ...
PloS one 10 (8), e0136501, 2015
1072015
The ‘hot cross bun’sign in the patients with spinocerebellar ataxia
YC Lee, CS Liu, HM Wu, PS Wang, MH Chang, BW Soong
European journal of neurology 16 (4), 513-516, 2009
1072009
Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese
YC Lee, CS Liu, MH Chang, KP Lin, JL Fuh, YC Lu, YF Liu, BW Soong
Journal of neurology 256, 249-255, 2009
1042009
A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy
PC Tsai, BW Soong, I Mademan, YH Huang, CR Liu, CT Hsiao, HT Wu, ...
Brain 140 (5), 1252-1266, 2017
932017
Safety and efficacy of rozanolixizumab in patients with generalised myasthenia gravis (MycarinG): a randomised, double-blind, placebo-controlled, adaptive phase 3 study
V Bril, A Drużdż, J Grosskreutz, AA Habib, R Mantegazza, S Sacconi, ...
The Lancet Neurology 22 (5), 383-394, 2023
842023
FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS
CP Tsai, BW Soong, KP Lin, PH Tu, JL Lin, YC Lee
Neurobiology of aging 32 (3), 553. e13-553. e21, 2011
812011
Mutations in ATP1A1 cause dominant Charcot-Marie-Tooth type 2
P Lassuthova, AP Rebelo, G Ravenscroft, PJ Lamont, MR Davis, ...
The American Journal of Human Genetics 102 (3), 505-514, 2018
792018
Mutational analysis of MATR3 in Taiwanese patients with amyotrophic lateral sclerosis
KP Lin, PC Tsai, YC Liao, WT Chen, CP Tsai, BW Soong, YC Lee
Neurobiology of aging 36 (5), 2005. e1-2005. e4, 2015
752015
A hexanucleotide repeat expansion in C9ORF72 causes familial and sporadic ALS in Taiwan
CP Tsai, BW Soong, PH Tu, KP Lin, JL Fuh, PC Tsai, YC Lu, IH Lee, ...
Neurobiology of aging 33 (9), 2232. e11-2232. e18, 2012
702012
Cognitive reserve: a SPECT study of 132 Alzheimer’s disease patients with an education range of 0–19 years
YC Liao, RS Liu, EL Teng, YC Lee, PN Wang, KN Lin, CP Chung, HC Liu
Dementia and geriatric cognitive disorders 20 (1), 8-14, 2005
692005
Comparison of cerebellar ataxias: A three‐year prospective longitudinal assessment
Y Lee, Y Liao, P Wang, IH Lee, K Lin, B Soong
Movement Disorders 26 (11), 2081-2087, 2011
672011
PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defects
YT Liu, FS Nian, WJ Chou, CY Tai, SY Kwan, C Chen, PW Kuo, PH Lin, ...
Oncotarget 7 (26), 39184, 2016
662016
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