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Association Analysis of COQ2 Variant in Dementia and Essential Tremor.
Chao YX, Ng EY, Li H, Nagaendran K, Yih Y, Chong MS, Prakash KM, Tan L, Au WL, Zhao Y, Zhou ZD, Tio M, Pavanni R, Tan EK. Chao YX, et al. Among authors: zhao y. Parkinsons Dis. 2015;2015:926280. doi: 10.1155/2015/926280. Epub 2015 Apr 22. Parkinsons Dis. 2015. PMID: 25977831 Free PMC article.
Genetic analysis of Nurr1 haplotypes in Parkinson's disease.
Tan EK, Chung H, Zhao Y, Shen H, Chandran VR, Tan C, Teoh ML, Yih Y, Pavanni R, Wong MC. Tan EK, et al. Among authors: zhao y. Neurosci Lett. 2003 Aug 28;347(3):139-42. doi: 10.1016/s0304-3940(03)00539-1. Neurosci Lett. 2003. PMID: 12875905
Nurr1 mutational screen in Parkinson's disease.
Tan EK, Chung H, Chandran VR, Tan C, Shen H, Yew K, Pavanni R, Puvan KA, Wong MC, Teoh ML, Yih Y, Zhao Y. Tan EK, et al. Among authors: zhao y. Mov Disord. 2004 Dec;19(12):1503-5. doi: 10.1002/mds.20246. Mov Disord. 2004. PMID: 15390059
PINK1 mutations in sporadic early-onset Parkinson's disease.
Tan EK, Yew K, Chua E, Puvan K, Shen H, Lee E, Puong KY, Zhao Y, Pavanni R, Wong MC, Jamora D, de Silva D, Moe KT, Woon FP, Yuen Y, Tan L. Tan EK, et al. Among authors: zhao y. Mov Disord. 2006 Jun;21(6):789-93. doi: 10.1002/mds.20810. Mov Disord. 2006. PMID: 16482571
Case-control study of UCHL1 S18Y variant in Parkinson's disease.
Tan EK, Puong KY, Fook-Chong S, Chua E, Shen H, Yuen Y, Pavanni R, Wong MC, Puvan K, Zhao Y. Tan EK, et al. Among authors: zhao y. Mov Disord. 2006 Oct;21(10):1765-8. doi: 10.1002/mds.21064. Mov Disord. 2006. PMID: 16941465
87,492 results
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