Bing-wen Soong
Bing-wen Soong
Taipei Medical University & National Yang-Ming University
在 的電子郵件地址已通過驗證
Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria
MK Bruno, M Hallett, K Gwinn-Hardy, B Sorensen, E Considine, S Tucker, ...
Neurology 63 (12), 2280-2287, 2004
Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions
HY Lee, Y Huang, N Bruneau, P Roll, EDO Roberson, M Hermann, ...
Cell reports 1 (1), 2-12, 2012
Increased oxidative damage and mitochondrial abnormalities in the peripheral blood of Huntington’s disease patients
CM Chen, YR Wu, ML Cheng, JL Liu, YM Lee, PW Lee, BW Soong, ...
Biochemical and biophysical research communications 359 (2), 335-340, 2007
Spinocerebellar ataxias: an update
B Soong, HL Paulson
Current opinion in neurology 20 (4), 438-446, 2007
Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studies
KJ Swoboda, BW Soong, C McKenna, ERP Brunt, M Litt, JF Bale, ...
Neurology 55 (2), 224-230, 2000
Clinical spectrum of Niemann‐Pick disease type C
JK Fink, MR Filling-Katz, J Sokol, DG Cogan, A Pikus, B Sonies, B Soong, ...
Neurology 39 (8), 1040-1040, 1989
Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study
C Gaspar, I Lopes-Cendes, S Hayes, J Goto, K Arvidsson, A Dias, ...
The American Journal of Human Genetics 68 (2), 523-528, 2001
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
Spinocerebellar ataxia type 2 presenting as familial levodopa‐responsive parkinsonism
DE Shan, BW Soong, CM Sun, SJ Lee, KK Liao, RS Liu
Annals of neurology 50 (6), 812-815, 2001
Impairments in cognitive function and brain connectivity in severe asymptomatic carotid stenosis
HL Cheng, CJ Lin, BW Soong, PN Wang, FC Chang, YT Wu, KH Chou, ...
Stroke 43 (10), 2567-2573, 2012
A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21‐q23
M Chung, YC Lu, NC Cheng, BW Soong
Brain 126 (6), 1293-1299, 2003
Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion
M Labuda, D Labuda, C Miranda, J Poirier, BW Soong, NE Barucha, ...
Neurology 54 (12), 2322-2324, 2000
Frequency analysis of autosomal dominant cerebellar ataxias in Taiwanese patients and clinical and molecular characterization of spinocerebellar ataxia type 6
B Soong, Y Lu, K Choo, H Lee
Archives of neurology 58 (7), 1105-1109, 2001
Dysregulation of C/EBPα by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease
MC Chiang, HM Chen, YH Lee, HH Chang, YC Wu, BW Soong, CM Chen, ...
Human molecular genetics 16 (5), 483-498, 2007
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 (2), 249-255, 2009
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
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
Fractal dimension analysis for quantifying cerebellar morphological change of multiple system atrophy of the cerebellar type (MSA-C)
YT Wu, KK Shyu, CW Jao, ZY Wang, BW Soong, HM Wu, PS Wang
Neuroimage 49 (1), 539-551, 2010
Mesenchymal stem cell transplantation ameliorates motor function deterioration of spinocerebellar ataxia by rescuing cerebellar Purkinje cells
YK Chang, MH Chen, YH Chiang, YF Chen, WH Ma, CY Tseng, ...
Journal of biomedical science 18 (1), 1-9, 2011
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
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