Wong V - Search Results

1

Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.

Guo Y, Baum LW, Sham PC, Wong V, Ng PW, Lui CH, Sin NC, Tsoi TH, Tang CS, Kwan JS, Yip BH, Xiao SM, Thomas GN, Lau YL, Yang W, Cherny SS, Kwan P. Guo Y, et al. Among authors: wong v. Hum Mol Genet. 2012 Mar 1;21(5):1184-9. doi: 10.1093/hmg/ddr550. Epub 2011 Nov 24. Hum Mol Genet. 2012. PMID: 22116939

2

Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy.

Baum L, Haerian BS, Ng HK, Wong VC, Ng PW, Lui CH, Sin NC, Zhang C, Tomlinson B, Wong GW, Tan HJ, Raymond AA, Mohamed Z, Kwan P. Baum L, et al. Hum Genet. 2014 May;133(5):651-9. doi: 10.1007/s00439-013-1405-1. Epub 2013 Dec 13. Hum Genet. 2014. PMID: 24337656

3

Gene-wide tagging study of association between ABCB1 polymorphisms and multidrug resistance in epilepsy in Han Chinese.

Kwan P, Wong V, Ng PW, Lui CH, Sin NC, Poon WS, Ng HK, Wong KS, Baum L. Kwan P, et al. Among authors: wong v, wong ks. Pharmacogenomics. 2009 May;10(5):723-32. doi: 10.2217/pgs.09.32. Pharmacogenomics. 2009. PMID: 19450124

4

Gene-wide tagging study of the association between ABCC2, ABCC5 and ABCG2 genetic polymorphisms and multidrug resistance in epilepsy.

Kwan P, Wong V, Ng PW, Lui CH, Sin NC, Wong KS, Baum L. Kwan P, et al. Among authors: wong v, wong ks. Pharmacogenomics. 2011 Mar;12(3):319-25. doi: 10.2217/pgs.10.183. Pharmacogenomics. 2011. PMID: 21449672

5

Association between ABCB1 C3435T polymorphism and drug-resistant epilepsy in Han Chinese.

Kwan P, Baum L, Wong V, Ng PW, Lui CH, Sin NC, Hui AC, Yu E, Wong LK. Kwan P, et al. Among authors: wong lk, wong v. Epilepsy Behav. 2007 Aug;11(1):112-7. doi: 10.1016/j.yebeh.2007.04.013. Epub 2007 May 22. Epilepsy Behav. 2007. PMID: 17521963

6

Multidrug resistance in epilepsy and polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, and SCN3A: correlation among phenotype, genotype, and mRNA expression.

Kwan P, Poon WS, Ng HK, Kang DE, Wong V, Ng PW, Lui CH, Sin NC, Wong KS, Baum L. Kwan P, et al. Among authors: wong v, wong ks. Pharmacogenet Genomics. 2008 Nov;18(11):989-98. doi: 10.1097/FPC.0b013e3283117d67. Pharmacogenet Genomics. 2008. PMID: 18784617

7

Deletions, duplications and novel restriction fragment length polymorphism in Duchenne and Becker muscular dystrophies.

Lau YL, Srivastava G, Wong V, Liu YT, Ho FC, Yeung CY. Lau YL, et al. Among authors: wong v. Clin Genet. 1992 May;41(5):252-8. doi: 10.1111/j.1399-0004.1992.tb03676.x. Clin Genet. 1992. PMID: 1351430

8

An epidemiological study of epilepsy in Hong Kong SAR, China.

Fong GC, Kwan P, Hui AC, Lui CH, Fong JK, Wong V. Fong GC, et al. Among authors: wong v. Seizure. 2008 Jul;17(5):457-64. doi: 10.1016/j.seizure.2007.12.005. Epub 2008 Feb 7. Seizure. 2008. PMID: 18261935 Free article.

9

Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese.

Mak CM, Lam CW, Siu TS, Chan KY, Siu WK, Yeung WL, Hui J, Wong VC, Low LC, Ko CH, Fung CW, Chen SP, Yuen YP, Lee HC, Yau E, Chan B, Tong SF, Tam S, Chan YW. Mak CM, et al. Among authors: wong vc. Mol Genet Metab. 2010 Apr;99(4):431-3. doi: 10.1016/j.ymgme.2009.12.011. Epub 2009 Dec 21. Mol Genet Metab. 2010. PMID: 20056467

10

Hypertransfusion for spinal cord compression secondary to extramedullary hematopoiesis.

Lee AC, Chiu W, Tai KS, Wong V, Peh WC, Lau YL. Lee AC, et al. Among authors: wong v. Pediatr Hematol Oncol. 1996 Jan-Feb;13(1):89-94. doi: 10.3109/08880019609033375. Pediatr Hematol Oncol. 1996. PMID: 8718506

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