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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: yuen 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: yuen y. Mov Disord. 2006 Oct;21(10):1765-8. doi: 10.1002/mds.21064. Mov Disord. 2006. PMID: 16941465
Expanded FMR1 alleles are rare in idiopathic Parkinson's disease.
Tan EK, Zhao Y, Puong KY, Law HY, Chan LL, Yew K, Shen H, Chandran VR, Yuen Y, Pavanni R, Wong MC, Ng IS. Tan EK, et al. Among authors: yuen y. Neurogenetics. 2005 Feb;6(1):51-2. doi: 10.1007/s10048-004-0200-5. Neurogenetics. 2005. PMID: 15742217 No abstract available.
Analysis of LRRK2 functional domains in nondominant Parkinson disease.
Skipper L, Shen H, Chua E, Bonnard C, Kolatkar P, Tan LC, Jamora RD, Puvan K, Puong KY, Zhao Y, Pavanni R, Wong MC, Yuen Y, Farrer M, Liu JJ, Tan EK. Skipper L, et al. Among authors: yuen y. Neurology. 2005 Oct 25;65(8):1319-21. doi: 10.1212/01.wnl.0000180517.70572.37. Neurology. 2005. PMID: 16247070
Genetic analysis of SCA2, 3 and 17 in idiopathic Parkinson's disease.
Lim SW, Zhao Y, Chua E, Law HY, Yuen Y, Pavanni R, Wong MC, Ng IS, Yoon CS, Puong KY, Lim SH, Tan EK. Lim SW, et al. Among authors: yuen y. Neurosci Lett. 2006 Jul 31;403(1-2):11-4. doi: 10.1016/j.neulet.2006.04.019. Epub 2006 May 9. Neurosci Lett. 2006. PMID: 16687213
Case control study of diffusion tensor imaging in Parkinson's disease.
Chan LL, Rumpel H, Yap K, Lee E, Loo HV, Ho GL, Fook-Chong S, Yuen Y, Tan EK. Chan LL, et al. Among authors: yuen y. J Neurol Neurosurg Psychiatry. 2007 Dec;78(12):1383-6. doi: 10.1136/jnnp.2007.121525. Epub 2007 Jul 5. J Neurol Neurosurg Psychiatry. 2007. PMID: 17615165 Free PMC article.
162 results