Tan EK - Search Results

1

Rare lysosomal enzyme gene SMPD1 variant (p.R591C) associates with Parkinson's disease.

Foo JN, Liany H, Bei JX, Yu XQ, Liu J, Au WL, Prakash KM, Tan LC, Tan EK. Foo JN, et al. Among authors: tan lc, tan ek. Neurobiol Aging. 2013 Dec;34(12):2890.e13-5. doi: 10.1016/j.neurobiolaging.2013.06.010. Epub 2013 Jul 18. Neurobiol Aging. 2013. PMID: 23871123

2

Evaluation of somnolence in Parkinson's disease: comparison with age- and sex-matched controls.

Tan EK, Lum SY, Fook-Chong SM, Teoh ML, Yih Y, Tan L, Tan A, Wong MC. Tan EK, et al. Among authors: tan a, tan l. Neurology. 2002 Feb 12;58(3):465-8. doi: 10.1212/wnl.58.3.465. Neurology. 2002. PMID: 11839852

3

The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.

Tan EK, Shen H, Tan LC, Farrer M, Yew K, Chua E, Jamora RD, Puvan K, Puong KY, Zhao Y, Pavanni R, Wong MC, Yih Y, Skipper L, Liu JJ. Tan EK, et al. Among authors: tan lc. Neurosci Lett. 2005 Aug 26;384(3):327-9. doi: 10.1016/j.neulet.2005.04.103. Neurosci Lett. 2005. PMID: 15955629 Clinical Trial.

4

Non-motor manifestations in essential tremor: use of a validated instrument to evaluate a wide spectrum of symptoms.

Tan EK, Fook-Chong S, Lum SY, Gabriel C, Koh KK, Prakash KM, Louis ED. Tan EK, et al. Parkinsonism Relat Disord. 2005 Sep;11(6):375-80. doi: 10.1016/j.parkreldis.2005.04.007. Parkinsonism Relat Disord. 2005. PMID: 16102997

5

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: tan lc, tan ek. Neurology. 2005 Oct 25;65(8):1319-21. doi: 10.1212/01.wnl.0000180517.70572.37. Neurology. 2005. PMID: 16247070

6

Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.

Skipper L, Li Y, Bonnard C, Pavanni R, Yih Y, Chua E, Sung WK, Tan L, Wong MC, Tan EK, Liu J. Skipper L, et al. Among authors: tan l, tan ek. Hum Mol Genet. 2005 Dec 1;14(23):3549-56. doi: 10.1093/hmg/ddi376. Epub 2005 Nov 3. Hum Mol Genet. 2005. PMID: 16269443

7

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: tan l. Mov Disord. 2006 Jun;21(6):789-93. doi: 10.1002/mds.20810. Mov Disord. 2006. PMID: 16482571

8

Analysis of 14 LRRK2 mutations in Parkinson's plus syndromes and late-onset Parkinson's disease.

Tan EK, Skipper L, Chua E, Wong MC, Pavanni R, Bonnard C, Kolatkar P, Liu JJ. Tan EK, et al. Mov Disord. 2006 Jul;21(7):997-1001. doi: 10.1002/mds.20875. Mov Disord. 2006. PMID: 16602113

9

DYT1 mutations amongst adult primary dystonia patients in Singapore with review of literature comparing East and West.

Jamora RD, Tan EK, Liu CP, Kathirvel P, Burgunder JM, Tan LC. Jamora RD, et al. Among authors: tan lc, tan ek. J Neurol Sci. 2006 Aug 15;247(1):35-7. doi: 10.1016/j.jns.2006.03.009. Epub 2006 Apr 24. J Neurol Sci. 2006. PMID: 16631205 Free article.

10

Polymorphisms in candidate genes: implications for the current treatment of Parkinson's disease.

Skipper L, Liu JJ, Tan EK. Skipper L, et al. Among authors: tan ek. Expert Opin Pharmacother. 2006 May;7(7):849-55. doi: 10.1517/14656566.7.7.849. Expert Opin Pharmacother. 2006. PMID: 16634708 Review.

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