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A previously misdiagnosed cohort of aquaporin 4 antibody-positive neuromyelitis optica spectrum disorder with disease duration of >10 years in multi-ethnic Penang, Malaysia: Clinical features and disease course.
Hor JY, Lim TT, Chow HB, Tan K, Cheah CF, Ching YM, Arip M, Easaw PE, Eow GB. Hor JY, et al. Among authors: eow gb. Mult Scler Relat Disord. 2016 Jan;5:89-90. doi: 10.1016/j.msard.2015.11.008. Epub 2015 Nov 14. Mult Scler Relat Disord. 2016. PMID: 26856950 No abstract available.
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: eow gb. 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: eow gb. 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.
23 results