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Genetic study of early-onset Parkinson's disease in the Malaysian population.
Tay YW, Tan AH, Lim JL, Lohmann K, Ibrahim KA, Abdul Aziz Z, Chin YT, Mawardi AS, Lim TT, Looi I, Chia YK, Ooi JCE, Cheah WK, Dy Closas AMF, Lit LC, Hor JW, Toh TS, Muthusamy KA, Bauer P, Skrahin V, Rolfs A, Klein C, Ahmad-Annuar A, Lim SY. Tay YW, et al. Among authors: lim tt. Parkinsonism Relat Disord. 2023 Jun;111:105399. doi: 10.1016/j.parkreldis.2023.105399. Epub 2023 Apr 15. Parkinsonism Relat Disord. 2023. PMID: 37209484
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: lim sy, lim tt, lim sk. 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: lim sy, lim tt, lim sk. 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: lim sy, lim tt, lim jl, lim sk. 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.
Delivering patient-centered care in Parkinson's disease: Challenges and consensus from an international panel.
Bhidayasiri R, Panyakaew P, Trenkwalder C, Jeon B, Hattori N, Jagota P, Wu YR, Moro E, Lim SY, Shang H, Rosales R, Lee JY, Thit WM, Tan EK, Lim TT, Tran NT, Binh NT, Phoumindr A, Boonmongkol T, Phokaewvarangkul O, Thongchuam Y, Vorachit S, Plengsri R, Chokpatcharavate M, Fernandez HH. Bhidayasiri R, et al. Among authors: lim sy, lim tt. Parkinsonism Relat Disord. 2020 Mar;72:82-87. doi: 10.1016/j.parkreldis.2020.02.013. Epub 2020 Feb 27. Parkinsonism Relat Disord. 2020. PMID: 32146380
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: lim sy, lim tt, lim sk. 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: lim sy, lim tt. 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
152 results