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Page 1
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: puvan k. 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: puvan k. Mov Disord. 2006 Oct;21(10):1765-8. doi: 10.1002/mds.21064. Mov Disord. 2006. PMID: 16941465
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: puvan k. Neurology. 2005 Oct 25;65(8):1319-21. doi: 10.1212/01.wnl.0000180517.70572.37. Neurology. 2005. PMID: 16247070
Alpha-synuclein haplotypes implicated in risk of Parkinson's disease.
Tan EK, Chai A, Teo YY, Zhao Y, Tan C, Shen H, Chandran VR, Teoh ML, Yih Y, Pavanni R, Wong MC, Puvan K, Lo YL, Yap E. Tan EK, et al. Among authors: puvan k. Neurology. 2004 Jan 13;62(1):128-31. doi: 10.1212/01.wnl.0000101721.25345.dc. Neurology. 2004. PMID: 14718715
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: puvan k. 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.
Intramedullary spinal cord metastasis.
Lim SH, Puvan K. Lim SH, et al. Among authors: puvan k. Ann Acad Med Singap. 1989 May;18(3):324-5. Ann Acad Med Singap. 1989. PMID: 2774479
12 results