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Page 1
Lack of association between the LRRK2 A419V variant and Asian Parkinson's disease.
Gopalai AA, Lim SY, Aziz ZA, Lim SK, Tan LP, Chong YB, Tan CT, Puvanarajah S, Viswanathan S, Kuppusamy R, Tan AH, Lim TT, Eow GB, Norlinah MI, Li HH, Zhao Y, Ahmad-Annuar A. Gopalai AA, et al. Among authors: puvanarajah s. Ann Acad Med Singap. 2013 May;42(5):237-40. Ann Acad Med Singap. 2013. PMID: 23771111 Free article.
LRRK2 G2385R and R1628P mutations are associated with an increased risk of Parkinson's disease in the Malaysian population.
Gopalai AA, Lim SY, Chua JY, Tey S, Lim TT, Mohamed Ibrahim N, Tan AH, Eow GB, Abdul Aziz Z, Puvanarajah SD, Viswanathan S, Looi I, Lim SK, Tan LP, Chong YB, Tan CT, Zhao Y, Tan EK, Ahmad-Annuar A. Gopalai AA, et al. Among authors: puvanarajah sd. Biomed Res Int. 2014;2014:867321. doi: 10.1155/2014/867321. Epub 2014 Aug 28. Biomed Res Int. 2014. PMID: 25243190 Free PMC article.
LRRK2 N551K and R1398H variants are protective in Malays and Chinese in Malaysia: A case-control association study for Parkinson's disease.
Gopalai AA, Lim JL, Li HH, Zhao Y, Lim TT, Eow GB, Puvanarajah S, Viswanathan S, Norlinah MI, Abdul Aziz Z, Lim SK, Tan CT, Tan AH, Lim SY, Tan EK, Ahmad Annuar A. Gopalai AA, et al. Among authors: puvanarajah s. Mol Genet Genomic Med. 2019 Nov;7(11):e604. doi: 10.1002/mgg3.604. Epub 2019 Sep 5. Mol Genet Genomic Med. 2019. PMID: 31487119 Free PMC article.
PINK1 p.Leu347Pro mutations in Malays: Prevalence and illustrative cases.
Tan AH, Lohmann K, Tay YW, Lim JL, Ahmad-Annuar A, Ramli N, Chin YT, Mawardi AS, Azmi K, Aziz ZA, Puvanarajah SD, Bauer P, Klein C, Rolfs A, Lim SY. Tan AH, et al. Among authors: puvanarajah sd. Parkinsonism Relat Disord. 2020 Oct;79:34-39. doi: 10.1016/j.parkreldis.2020.08.015. Epub 2020 Aug 19. Parkinsonism Relat Disord. 2020. PMID: 32861104
Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestry.
Lim JL, Ng EY, Lim SY, Tan AH, Abdul-Aziz Z, Ibrahim KA, Gopalai AA, Tay YW, Vijayanathan Y, Toh TS, Lim SK, Bee PC, Puvanarajah SD, Viswanathan S, Looi I, Lim TT, Eow GB, Cheah WK, Tan EK, Ahmad-Annuar A. Lim JL, et al. Among authors: puvanarajah sd. Neurol Sci. 2021 Oct;42(10):4203-4207. doi: 10.1007/s10072-021-05056-x. Epub 2021 Feb 8. Neurol Sci. 2021. PMID: 33559030
Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: mutational spectrum and clinical features.
Lim JL, Lohmann K, Tan AH, Tay YW, Ibrahim KA, Abdul Aziz Z, Mawardi AS, Puvanarajah SD, Lim TT, Looi I, Ooi JCE, Chia YK, Muthusamy KA, Bauer P, Rolfs A, Klein C, Ahmad-Annuar A, Lim SY. Lim JL, et al. Among authors: puvanarajah sd. J Neural Transm (Vienna). 2022 Jan;129(1):37-48. doi: 10.1007/s00702-021-02421-0. Epub 2021 Nov 15. J Neural Transm (Vienna). 2022. PMID: 34779914
Validation of an informant-based cognitive screening tool for Parkinson disease.
Chee KY, Ong KY, Mak CY, Yacob S, Yeo SC, Thrichelam N, Amarnath DD, Thong KS, Moey CH, Ponusamy T, Viswanathan S, Puvanarajah S. Chee KY, et al. Among authors: puvanarajah s. Asia Pac Psychiatry. 2017 Dec;9(4). doi: 10.1111/appy.12278. Epub 2017 Mar 21. Asia Pac Psychiatry. 2017. PMID: 28326670
Prevalence study of epilepsy in Malaysia.
Fong SL, Lim KS, Tan L, Zainuddin NH, Ho JH, Chia ZJ, Choo WY, Puvanarajah SD, Chinnasami S, Tee SK, Raymond AA, Law WC, Tan CT. Fong SL, et al. Among authors: puvanarajah sd. Epilepsy Res. 2021 Feb;170:106551. doi: 10.1016/j.eplepsyres.2021.106551. Epub 2021 Jan 6. Epilepsy Res. 2021. PMID: 33440303
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