Chandran VR - Search Results

1

Differential expression of splice variant and wild-type parkin in sporadic Parkinson's disease.

Tan EK, Shen H, Tan JM, Lim KL, Fook-Chong S, Hu WP, Paterson MC, Chandran VR, Yew K, Tan C, Yuen Y, Pavanni R, Wong MC, Puvan K, Zhao Y. Tan EK, et al. Among authors: chandran vr. Neurogenetics. 2005 Dec;6(4):179-84. doi: 10.1007/s10048-005-0001-5. Epub 2005 Aug 6. Neurogenetics. 2005. PMID: 16086186

2

Alpha-synuclein mRNA expression in sporadic Parkinson's disease.

Tan EK, Chandran VR, Fook-Chong S, Shen H, Yew K, Teoh ML, Yuen Y, Zhao Y. Tan EK, et al. Among authors: chandran vr. Mov Disord. 2005 May;20(5):620-3. doi: 10.1002/mds.20391. Mov Disord. 2005. PMID: 15719423

3

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: chandran vr. Neurosci Lett. 2003 Aug 28;347(3):139-42. doi: 10.1016/s0304-3940(03)00539-1. Neurosci Lett. 2003. PMID: 12875905

4

Dose-dependent protective effect of coffee, tea, and smoking in Parkinson's disease: a study in ethnic Chinese.

Tan EK, Tan C, Fook-Chong SM, Lum SY, Chai A, Chung H, Shen H, Zhao Y, Teoh ML, Yih Y, Pavanni R, Chandran VR, Wong MC. Tan EK, et al. Among authors: chandran vr. J Neurol Sci. 2003 Dec 15;216(1):163-7. doi: 10.1016/j.jns.2003.07.006. J Neurol Sci. 2003. PMID: 14607318

5

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: chandran vr. Neurology. 2004 Jan 13;62(1):128-31. doi: 10.1212/01.wnl.0000101721.25345.dc. Neurology. 2004. PMID: 14718715

6

Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort.

Tan EK, Zhao Y, Puong KY, Law HY, Chan LL, Yew K, Tan C, Shen H, Chandran VR, Teoh ML, Yih Y, Pavanni R, Wong MC, Ng IS. Tan EK, et al. Among authors: chandran vr. Neurology. 2004 Jul 27;63(2):362-3. doi: 10.1212/01.wnl.0000130199.57181.7b. Neurology. 2004. PMID: 15277639

7

Genetic analysis of DJ-1 in a cohort Parkinson's disease patients of different ethnicity.

Tan EK, Tan C, Zhao Y, Yew K, Shen H, Chandran VR, Teoh ML, Yih Y, Pavanni R, Wong MC. Tan EK, et al. Among authors: chandran vr. Neurosci Lett. 2004 Aug 26;367(1):109-12. doi: 10.1016/j.neulet.2004.05.090. Neurosci Lett. 2004. PMID: 15308309

8

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: chandran vr. Neurogenetics. 2005 Feb;6(1):51-2. doi: 10.1007/s10048-004-0200-5. Neurogenetics. 2005. PMID: 15742217 No abstract available.

9

Functional COMT variant predicts response to high dose pyridoxine in Parkinson's disease.

Tan EK, Cheah SY, Fook-Chong S, Yew K, Chandran VR, Lum SY, Yi Z. Tan EK, et al. Among authors: chandran vr. Am J Med Genet B Neuropsychiatr Genet. 2005 Aug 5;137B(1):1-4. doi: 10.1002/ajmg.b.30198. Am J Med Genet B Neuropsychiatr Genet. 2005. PMID: 15965967 Clinical Trial.

10

Enhanced Activity of Topical Hydrocortisone by Competitive Binding of Corticosteroid-Binding Globulin.

Bodor ET, Wu WM, Chandran VR, Bodor N. Bodor ET, et al. Among authors: chandran vr. J Pharm Sci. 2016 Sep;105(9):2873-2878. doi: 10.1016/j.xphs.2016.03.028. Epub 2016 May 11. J Pharm Sci. 2016. PMID: 27179671

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