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Page 1
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: puong ky. Mov Disord. 2006 Oct;21(10):1765-8. doi: 10.1002/mds.21064. Mov Disord. 2006. PMID: 16941465
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: puong ky. Mov Disord. 2006 Jun;21(6):789-93. doi: 10.1002/mds.20810. Mov Disord. 2006. PMID: 16482571
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: puong ky. 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: puong ky. 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
Analysis of PINK1 in Asian patients with familial parkinsonism.
Tan EK, Yew K, Chua E, Shen H, Jamora RD, Lee E, Puong KY, Zhao Y, Pavanni R, Wong MC, Puvan K, Yih Y, Tan LC. Tan EK, et al. Among authors: puong ky. Clin Genet. 2005 Nov;68(5):468-70. doi: 10.1111/j.1399-0004.2005.00500.x. Clin Genet. 2005. PMID: 16207217 No abstract available.
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: puong ky. Neurogenetics. 2005 Feb;6(1):51-2. doi: 10.1007/s10048-004-0200-5. Neurogenetics. 2005. PMID: 15742217 No abstract available.
16 results