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Wong Meng Cheong

rp24506

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Full Name
Wong Meng Cheong
(not current staff)
Main Affiliation
 
Faculty
 
Email
phcwong@nus.edu.sg
 
Other emails
 

Publications

Results 1-20 of 22 (Search time: 0.007 seconds).

Issue DateTitleAuthor(s)
12007Acute ataxia, Graves' disease, and stiff person syndromeChia S.-Y.; Chua R.; Lo Y.-L. ; Wong M.-C. ; Chan L.-L. ; Tan E.-K. 
22004Alpha-synuclein haplotypes implicated in risk of Parkinson's diseaseTan E.-K. ; Chai A.; Teo Y.Y. ; Zhao Y.; Tan C.; Shen H.; Chandran V.R.; Teoh M.L.; Yih Y.; Pavanni R. ; Wong M.C. ; Puvan K. ; Lo Y.L. ; Yap E. 
32006Analysis of 14 LRRK2 mutations in Parkinson's plus syndromes and late-onset Parkinson's diseaseTan E.-K. ; Skipper L.; Chua E.; Wong M.-C. ; Pavanni R. ; Bonnard C.; Kolatkar P. ; Liu J.-J.
42005Analysis of LRRK2 functional domains in nondominant Parkinson diseaseSkipper L.; Shen H.; Chua E.; Bonnard C.; Kolatkar P. ; Tan L.C.S. ; Jamora R.D.; Puvan K. ; Puong K.Y.; Zhao Y.; Pavanni R. ; Wong M.C. ; Yuen Y. ; Farrer M.; Liu J.J. ; Tan E.K. 
52005Analysis of PINK1 in Asian patients with familial parkinsonism [1]Tan E.-K. ; Yew K.; Chua E.; Shen H.; Jamora R.D.; Lee E.; Puong K.Y.; Zhao Y.; Pavanni R. ; Wong M.C. ; Puvan K. ; Yih Y.; Tan L.C.S. 
62005Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's diseaseSkipper L.; Li Y.; Bonnard C.; Pavanni R. ; Yih Y.; Chua E.; Sung W.-K. ; Tan L. ; Wong M.-C. ; Tan E.-K. ; Liu J. 
72002Diffusion Weighted MR Imaging in Acute Stroke: The SGH ExperienceChan L.L. ; Khoo J.B.K. ; Thng C.H. ; Lim W.E.H. ; Tay K.H. ; Tan E.K. ; Chang H.M. ; Chen C. ; Wong M.C. ; Tan K.P.
82003Dopamine D2 receptor taqIA and TaqIB polymorphisms in Parkinson's diseaseTan E.-K. ; Tan Y.; Chai A.; Tan C.; Shen H.; Lum S.Y.; Fook-Cheong S.M.C. ; Teoh M.-L.; Yih Y.; Wong M.-C. ; Zhao Y.
92003Dose-dependent protective effect of coffee, tea, and smoking in Parkinson's disease: A study in ethnic ChineseTan E.-K. ; Tan C.; Fook-Chong S.M.C. ; Lum S.Y.; Chai A.; Chung H.; Shen H.; Zhao Y.; Teoh M.L.; Yih Y.; Pavanni R. ; Chandran V.R.; Wong M.C. 
102007DRD3 variant and risk of essential tremorTan E.-K. ; Prakash K.M. ; Fook-Chong S. ; Yih Y.; Chua E.; Lum S.Y.; Wong M.C. ; Pavanni R. ; Zhao Y.
112005Expanded FMR1 alleles are rare in idiopathic Parkinson's disease [3]Tan E.K. ; Zhao Y.; Puong K.Y.; Law H.Y. ; Chan L.L. ; Yew K.; Shen H.; Chandran V.R.; Yuen Y. ; Pavanni R. ; Wong M.C. ; Ng I.S.
122004Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohortTan E.K. ; Zhao Y.; Puong K.Y.; Law H.Y. ; Chan L.L. ; Yew K.; Tan C.; Shen H.; Chandran V.R.; Teoh M.L.; Yih Y.; Pavanni R. ; Wong M.C. ; Ng I.S.
132004Genetic analysis of DJ-1 in a cohort Parkinson's disease patients of different ethnicityTan E.-K. ; Tan C.; Zhao Y.; Yew K.; Shen H.; Chandran V.R.; Teoh M.-L.; Yih Y.; Pavanni R. ; Wong M.-C. 
142003Genetic analysis of Nurr1 haplotypes in Parkinson's diseaseTan E.-K. ; Chung H.; Zhao Y.; Shen H.; Chandran V.R.; Tan C.; Teoh M.-L.; Yih Y.; Pavanni R. ; Wong M.-C. 
152007Genetic analysis of SCA 2 and 3 repeat expansions in essential tremor and atypical ParkinsonismTan E.-K. ; Tong J.; Pavanni R. ; Wong M.-C. ; Zhao Y.
162007Glucocerebrosidase mutations and risk of Parkinson disease in Chinese patients [2]Tan E.-K. ; Tong J.; Fook-Chong S. ; Yih Y. ; Wong M.-C. ; Pavanni R. ; Zhao Y.
172005Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition: Clinical associationTan E.K. ; Puong K.Y.; Chan D.K.Y.; Yew K.; Fook-Chong S. ; Shen H.; Ng P.W.; Woo J.; Yuen Y. ; Pavanni R. ; Wong M.C. ; Puvan K. ; Zhao Y.
1813-Dec-2021Long-Term Post-Stroke Functional Outcomes: A Comparison of Diabetics and NondiabeticsDe Silva D.A.; Narasimhalu K.; Huang I.W.; Woon F.P.; Allen J.C.; Wong M.C. 
192004MDR1, the blood-brain barrier transporter, is associated with Parkinson's disease in ethnic ChineseLee C.G. ; Tang K.; Cheung Y.B. ; Wong L.P.; Tan C.; Shen H.; Zhao Y.; Pavanni R. ; Lee E.J. ; Wong M.C. ; Chong S.S. ; Tan E.K. 
202004Nurr1 mutational screen in Parkinson's diseaseTan E.-K. ; Chung H.; Chandran V.R.; Tan C.; Shen H.; Yew K.; Pavanni R. ; Puvan K.-A. ; Wong M.-C. ; Teoh M.-L.; Yih Y.; Zhao Y.