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Items: 1 to 20 of 75

1.

A case of refractory seizure with cognitive impairment due to anti-GABA encephalitis.

Hui AT, Lam YO, Chan CK, Cheung KY, Fung BH, Ng PW.

Hong Kong Med J. 2016 Oct;22(5):509-11. doi: 10.12809/hkmj154604. No abstract available.

2.

A Pilot Study on the Efficacy of Volunteer Mentorship for Young Adults With Self-Harm Behaviors Using a Quasi-Experimental Design.

Law YW, Yip PS, Lai CC, Kwok CL, Wong PW, Liu KS, Ng PW, Liao CW, Wong TW.

Crisis. 2016 Nov;37(6):415-426. doi: 10.1027/0227-5910/a000393. Epub 2016 Jun 9.

PMID:
27278570
3.

Rationale and design of the PreventIon of CArdiovascular events in iSchemic Stroke patients with high risk of cerebral hemOrrhage (PICASSO) study: A randomized controlled trial.

Hong KS, Kim BJ, Lee JY, Kwon SU; PICASSO Investigators.

Int J Stroke. 2015 Oct;10(7):1153-8. doi: 10.1111/ijs.12519. Epub 2015 Jun 4.

PMID:
26044566
4.

Asian and Oceanian Congress of Neurology 2014: intraregional and interregional synergy.

Mehndiratta MM, Kaji R, Wong KS, Ng PW, Gulati NS.

Neurology. 2015 Mar 24;84(12):1269-71. doi: 10.1212/WNL.0000000000001388. No abstract available.

PMID:
25802270
5.

Evolution of intracranial atherosclerotic disease under modern medical therapy.

Leung TW, Wang L, Soo YO, Ip VH, Chan AY, Au LW, Fan FS, Lau AY, Leung H, Abrigo J, Wong A, Mok VC, Ng PW, Tsoi TH, Li SH, Man CB, Fong WC, Wong KS, Yu SC.

Ann Neurol. 2015 Mar;77(3):478-86. doi: 10.1002/ana.24340. Epub 2015 Jan 29.

PMID:
25557926
6.

Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies.

International League Against Epilepsy Consortium on Complex Epilepsies. Electronic address: epilepsy-austin@unimelb.edu.au.

Lancet Neurol. 2014 Sep;13(9):893-903. doi: 10.1016/S1474-4422(14)70171-1. Epub 2014 Jul 30.

7.

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.

Hum Genet. 2014 May;133(5):651-9. doi: 10.1007/s00439-013-1405-1. Epub 2013 Dec 13.

PMID:
24337656
8.

Genetic susceptibility to refractive error: association of vasoactive intestinal peptide receptor 2 (VIPR2) with high myopia in Chinese.

Yiu WC, Yap MK, Fung WY, Ng PW, Yip SP.

PLoS One. 2013 Apr 18;8(4):e61805. doi: 10.1371/journal.pone.0061805. Print 2013.

9.

The role of the Ala746Thr variant in the ATP13A2 gene among Chinese patients with Parkinson's disease.

Chan AY, Baum L, Tang NL, Lau CY, Ng PW, Hui KF, Mizuno Y, Kwan JY, Mok VC, Kuo SH.

J Clin Neurosci. 2013 May;20(5):761-2. doi: 10.1016/j.jocn.2012.05.052. Epub 2013 Mar 20.

10.

A novel missense mutation in the NYX gene associated with high myopia.

Yip SP, Li CC, Yiu WC, Hung WH, Lam WW, Lai MC, Ng PW, Fung WY, Chu PH, Jiang B, Chan HH, Yap MK.

Ophthalmic Physiol Opt. 2013 May;33(3):346-53. doi: 10.1111/opo.12036. Epub 2013 Feb 14.

PMID:
23406521
11.

Investigating the relationship between UMODL1 gene polymorphisms and high myopia: a case-control study in Chinese.

Zhu MM, Yap MK, Ho DW, Fung WY, Ng PW, Gu YS, Yip SP.

BMC Med Genet. 2012 Aug 2;13:64. doi: 10.1186/1471-2350-13-64.

12.

Association of high myopia with crystallin beta A4 (CRYBA4) gene polymorphisms in the linkage-identified MYP6 locus.

Ho DW, Yap MK, Ng PW, Fung WY, Yip SP.

PLoS One. 2012;7(6):e40238. doi: 10.1371/journal.pone.0040238. Epub 2012 Jun 29.

13.

Association of IGF1 gene haplotypes with high myopia in Chinese adults.

Mak JY, Yap MK, Fung WY, Ng PW, Yip SP.

Arch Ophthalmol. 2012 Feb;130(2):209-16. doi: 10.1001/archophthalmol.2011.365.

PMID:
22332214
14.

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.

Hum Mol Genet. 2012 Mar 1;21(5):1184-9. doi: 10.1093/hmg/ddr550. Epub 2011 Nov 24.

PMID:
22116939
15.

Genotyping performance assessment of whole genome amplified DNA with respect to multiplexing level of assay and its period of storage.

Ho DW, Yiu WC, Yap MK, Fung WY, Ng PW, Yip SP.

PLoS One. 2011;6(10):e26119. doi: 10.1371/journal.pone.0026119. Epub 2011 Oct 11.

16.

A study of deliberate self-harm and its repetition among patients presenting to an emergency department.

Yip PS, Hawton K, Liu K, Liu KS, Ng PW, Kam PM, Law YW, Wong TW.

Crisis. 2011;32(4):217-24. doi: 10.1027/0227-5910/a000069.

PMID:
21940251
17.

Presenile dementia: a case of Hashimoto's encephalopathy.

Chong CS, Leung JL, Wong IH, Ng PW, Miao MY.

East Asian Arch Psychiatry. 2011 Mar;21(1):32-6.

18.

A new Chinese terminology for dementia and cognitive impairment.

Working Group on New Chinese Terminology for Dementia and Cognitive Impairment.

Hong Kong Med J. 2011 Aug;17(4):342. No abstract available.

PMID:
21813909
19.

Evaluation of proteoglycan gene polymorphisms as risk factors in the genetic susceptibility to high myopia.

Yip SP, Leung KH, Ng PW, Fung WY, Sham PC, Yap MK.

Invest Ophthalmol Vis Sci. 2011 Aug 16;52(9):6396-403. doi: 10.1167/iovs.11-7639.

PMID:
21743019
20.

PAX6 haplotypes are associated with high myopia in Han chinese.

Jiang B, Yap MK, Leung KH, Ng PW, Fung WY, Lam WW, Gu YS, Yip SP.

PLoS One. 2011 May 12;6(5):e19587. doi: 10.1371/journal.pone.0019587.

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