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Items: 1 to 50 of 71

1.

Analysis of shared heritability in common disorders of the brain.

Brainstorm Consortium, Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, Lee PH, Turley P, Grenier-Boley B, Chouraki V, Kamatani Y, Berr C, Letenneur L, Hannequin D, Amouyel P, Boland A, Deleuze JF, Duron E, Vardarajan BN, Reitz C, Goate AM, Huentelman MJ, Kamboh MI, Larson EB, Rogaeva E, St George-Hyslop P, Hakonarson H, Kukull WA, Farrer LA, Barnes LL, Beach TG, Demirci FY, Head E, Hulette CM, Jicha GA, Kauwe JSK, Kaye JA, Leverenz JB, Levey AI, Lieberman AP, Pankratz VS, Poon WW, Quinn JF, Saykin AJ, Schneider LS, Smith AG, Sonnen JA, Stern RA, Van Deerlin VM, Van Eldik LJ, Harold D, Russo G, Rubinsztein DC, Bayer A, Tsolaki M, Proitsi P, Fox NC, Hampel H, Owen MJ, Mead S, Passmore P, Morgan K, Nöthen MM, Rossor M, Lupton MK, Hoffmann P, Kornhuber J, Lawlor B, McQuillin A, Al-Chalabi A, Bis JC, Ruiz A, Boada M, Seshadri S, Beiser A, Rice K, van der Lee SJ, De Jager PL, Geschwind DH, Riemenschneider M, Riedel-Heller S, Rotter JI, Ransmayr G, Hyman BT, Cruchaga C, Alegret M, Winsvold B, Palta P, Farh KH, Cuenca-Leon E, Furlotte N, Kurth T, Ligthart L, Terwindt GM, Freilinger T, Ran C, Gordon SD, Borck G, Adams HHH, Lehtimäki T, Wedenoja J, Buring JE, Schürks M, Hrafnsdottir M, Hottenga JJ, Penninx B, Artto V, Kaunisto M, Vepsäläinen S, Martin NG, Montgomery GW, Kurki MI, Hämäläinen E, Huang H, Huang J, Sandor C, Webber C, Muller-Myhsok B, Schreiber S, Salomaa V, Loehrer E, Göbel H, Macaya A, Pozo-Rosich P, Hansen T, Werge T, Kaprio J, Metspalu A, Kubisch C, Ferrari MD, Belin AC, van den Maagdenberg AMJM, Zwart JA, Boomsma D, Eriksson N, Olesen J, Chasman DI, Nyholt DR, Avbersek A, Baum L, Berkovic S, Bradfield J, Buono R, Catarino CB, Cossette P, De Jonghe P, Depondt C, Dlugos D, Ferraro TN, French J, Hjalgrim H, Jamnadas-Khoda J, Kälviäinen R, Kunz WS, Lerche H, Leu C, Lindhout D, Lo W, Lowenstein D, McCormack M, Møller RS, Molloy A, Ng PW, Oliver K, Privitera M, Radtke R, Ruppert AK, Sander T, Schachter S, Schankin C, Scheffer I, Schoch S, Sisodiya SM, Smith P, Sperling M, Striano P, Surges R, Thomas GN, Visscher F, Whelan CD, Zara F, Heinzen EL, Marson A, Becker F, Stroink H, Zimprich F, Gasser T, Gibbs R, Heutink P, Martinez M, Morris HR, Sharma M, Ryten M, Mok KY, Pulit S, Bevan S, Holliday E, Attia J, Battey T, Boncoraglio G, Thijs V, Chen WM, Mitchell B, Rothwell P, Sharma P, Sudlow C, Vicente A, Markus H, Kourkoulis C, Pera J, Raffeld M, Silliman S, Boraska Perica V, Thornton LM, Huckins LM, William Rayner N, Lewis CM, Gratacos M, Rybakowski F, Keski-Rahkonen A, Raevuori A, Hudson JI, Reichborn-Kjennerud T, Monteleone P, Karwautz A, Mannik K, Baker JH, O'Toole JK, Trace SE, Davis OSP, Helder SG, Ehrlich S, Herpertz-Dahlmann B, Danner UN, van Elburg AA, Clementi M, Forzan M, Docampo E, Lissowska J, Hauser J, Tortorella A, Maj M, Gonidakis F, Tziouvas K, Papezova H, Yilmaz Z, Wagner G, Cohen-Woods S, Herms S, Julià A, Rabionet R, Dick DM, Ripatti S, Andreassen OA, Espeseth T, Lundervold AJ, Steen VM, Pinto D, Scherer SW, Aschauer H, Schosser A, Alfredsson L, Padyukov L, Halmi KA, Mitchell J, Strober M, Bergen AW, Kaye W, Szatkiewicz JP, Cormand B, Ramos-Quiroga JA, Sánchez-Mora C, Ribasés M, Casas M, Hervas A, Arranz MJ, Haavik J, Zayats T, Johansson S, Williams N, Dempfle A, Rothenberger A, Kuntsi J, Oades RD, Banaschewski T, Franke B, Buitelaar JK, Arias Vasquez A, Doyle AE, Reif A, Lesch KP, Freitag C, Rivero O, Palmason H, Romanos M, Langley K, Rietschel M, Witt SH, Dalsgaard S, Børglum AD, Waldman I, Wilmot B, Molly N, Bau CHD, Crosbie J, Schachar R, Loo SK, McGough JJ, Grevet EH, Medland SE, Robinson E, Weiss LA, Bacchelli E, Bailey A, Bal V, Battaglia A, Betancur C, Bolton P, Cantor R, Celestino-Soper P, Dawson G, De Rubeis S, Duque F, Green A, Klauck SM, Leboyer M, Levitt P, Maestrini E, Mane S, De-Luca DM, Parr J, Regan R, Reichenberg A, Sandin S, Vorstman J, Wassink T, Wijsman E, Cook E, Santangelo S, Delorme R, Rogé B, Magalhaes T, Arking D, Schulze TG, Thompson RC, Strohmaier J, Matthews K, Melle I, Morris D, Blackwood D, McIntosh A, Bergen SE, Schalling M, Jamain S, Maaser A, Fischer SB, Reinbold CS, Fullerton JM, Guzman-Parra J, Mayoral F, Schofield PR, Cichon S, Mühleisen TW, Degenhardt F, Schumacher J, Bauer M, Mitchell PB, Gershon ES, Rice J, Potash JB, Zandi PP, Craddock N, Ferrier IN, Alda M, Rouleau GA, Turecki G, Ophoff R, Pato C, Anjorin A, Stahl E, Leber M, Czerski PM, Cruceanu C, Jones IR, Posthuma D, Andlauer TFM, Forstner AJ, Streit F, Baune BT, Air T, Sinnamon G, Wray NR, MacIntyre DJ, Porteous D, Homuth G, Rivera M, Grove J, Middeldorp CM, Hickie I, Pergadia M, Mehta D, Smit JH, Jansen R, de Geus E, Dunn E, Li QS, Nauck M, Schoevers RA, Beekman AT, Knowles JA, Viktorin A, Arnold P, Barr CL, Bedoya-Berrio G, Bienvenu OJ, Brentani H, Burton C, Camarena B, Cappi C, Cath D, Cavallini M, Cusi D, Darrow S, Denys D, Derks EM, Dietrich A, Fernandez T, Figee M, Freimer N, Gerber G, Grados M, Greenberg E, Hanna GL, Hartmann A, Hirschtritt ME, Hoekstra PJ, Huang A, Huyser C, Illmann C, Jenike M, Kuperman S, Leventhal B, Lochner C, Lyon GJ, Macciardi F, Madruga-Garrido M, Malaty IA, Maras A, McGrath L, Miguel EC, Mir P, Nestadt G, Nicolini H, Okun MS, Pakstis A, Paschou P, Piacentini J, Pittenger C, Plessen K, Ramensky V, Ramos EM, Reus V, Richter MA, Riddle MA, Robertson MM, Roessner V, Rosário M, Samuels JF, Sandor P, Stein DJ, Tsetsos F, Van Nieuwerburgh F, Weatherall S, Wendland JR, Wolanczyk T, Worbe Y, Zai G, Goes FS, McLaughlin N, Nestadt PS, Grabe HJ, Depienne C, Konkashbaev A, Lanzagorta N, Valencia-Duarte A, Bramon E, Buccola N, Cahn W, Cairns M, Chong SA, Cohen D, Crespo-Facorro B, Crowley J, Davidson M, DeLisi L, Dinan T, Donohoe G, Drapeau E, Duan J, Haan L, Hougaard D, Karachanak-Yankova S, Khrunin A, Klovins J, Kučinskas V, Lee Chee Keong J, Limborska S, Loughland C, Lönnqvist J, Maher B, Mattheisen M, McDonald C, Murphy KC, Nenadic I, van Os J, Pantelis C, Pato M, Petryshen T, Quested D, Roussos P, Sanders AR, Schall U, Schwab SG, Sim K, So HC, Stögmann E, Subramaniam M, Toncheva D, Waddington J, Walters J, Weiser M, Cheng W, Cloninger R, Curtis D, Gejman PV, Henskens F, Mattingsdal M, Oh SY, Scott R, Webb B, Breen G, Churchhouse C, Bulik CM, Daly M, Dichgans M, Faraone SV, Guerreiro R, Holmans P, Kendler KS, Koeleman B, Mathews CA, Price A, Scharf J, Sklar P, Williams J, Wood NW, Cotsapas C, Palotie A, Smoller JW, Sullivan P, Rosand J, Corvin A, Neale BM, Schott JM, Anney R, Elia J, Grigoroiu-Serbanescu M, Edenberg HJ, Murray R.

Science. 2018 Jun 22;360(6395). pii: eaap8757. doi: 10.1126/science.aap8757.

2.

Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis.

Wong JKL, Gui H, Kwok M, Ng PW, Lui CHT, Baum L, Sham PC, Kwan P, Cherny SS.

Neurol Genet. 2018 Jun 11;4(3):e245. doi: 10.1212/NXG.0000000000000245. eCollection 2018 Jun.

3.

The professional practice and training of neurology in the Asian and Oceanian Region: A cross-sectional survey by the Asian and Oceanian Association of Neurology (AOAN).

Roxas A Jr, Mehndiratta MM, Bornstein N, Macdonell R, Lim KS, Ng PW, Dashzeveg S, Mizusawa H, Esmatullah H, Wu SL, Chen C, Kurniawan M, Rha JH, Wasay M, Poungvarin N, Gunatilake S, Thang NH.

J Neurol Sci. 2017 Nov 15;382:108-115. doi: 10.1016/j.jns.2017.09.022. Epub 2017 Sep 20.

PMID:
29111001
4.

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.

5.

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
6.

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
7.

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
8.

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
9.

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.

10.

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.

11.

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
12.

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.

13.

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.

14.

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
15.

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
16.

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.

17.

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
18.

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.

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.

21.
22.

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.

Pharmacogenomics. 2011 Mar;12(3):319-25. doi: 10.2217/pgs.10.183. Erratum in: Pharmacogenomics. 2011 May;12(5):760.

PMID:
21449672
23.

Systematic investigation of the relationship between high myopia and polymorphisms of the MMP2, TIMP2, and TIMP3 genes by a DNA pooling approach.

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

Invest Ophthalmol Vis Sci. 2011 Jun 1;52(6):3893-900. doi: 10.1167/iovs.11-7286.

PMID:
21421877
24.

Announcement of a new Chinese name for epilepsy.

Lau KK, Ng PW, Chan CW, Lui C, Huang CY.

Epilepsia. 2011 Feb;52(2):420-1. doi: 10.1111/j.1528-1167.2010.02748.x. No abstract available.

25.

Failure to detect association between polymorphisms of the sodium channel gene SCN1A and febrile seizures in Chinese patients with epilepsy.

Zhang C, Wong V, Ng PW, Lui CH, Sin NC, Wong KS, Baum L, Kwan P.

Epilepsia. 2010 Sep;51(9):1878-81. doi: 10.1111/j.1528-1167.2010.02587.x.

26.

Effects of statins on progression of subclinical brain infarct.

Fu JH, Mok V, Lam W, Wong A, Chu W, Xiong Y, Ng PW, Tsoi TH, Yeung V, Wong KS.

Cerebrovasc Dis. 2010;30(1):51-6. doi: 10.1159/000313614. Epub 2010 Apr 29.

PMID:
20431290
27.

Prolonged myoclonus after a single bolus dose of propofol.

Tam MK, Irwin MG, Tse ML, Lui YW, Law KI, Ng PW.

Anaesthesia. 2009 Nov;64(11):1254-7. doi: 10.1111/j.1365-2044.2009.06035.x. Erratum in: Anaesthesia. 2010 Feb;65(2):222.

28.

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.

Pharmacogenomics. 2009 May;10(5):723-32. doi: 10.2217/pgs.09.32.

PMID:
19450124
29.

Effects of valproate or lamotrigine monotherapy on the reproductive endocrine and insulin-related metabolic profile in Chinese adults with epilepsy: a prospective randomized study.

Kwan P, Yip FP, Hui AC, Leung H, Ng PW, Hui KF, Chan IH, Chan MH, Lam CW.

Epilepsy Behav. 2009 Apr;14(4):610-6. doi: 10.1016/j.yebeh.2009.01.010. Epub 2009 Feb 8.

PMID:
19435587
30.

Statins for asymptomatic middle cerebral artery stenosis: The Regression of Cerebral Artery Stenosis study.

Mok VC, Lam WW, Chen XY, Wong A, Ng PW, Tsoi TH, Yeung V, Liu R, Soo Y, Leung TW, Wong KS.

Cerebrovasc Dis. 2009;28(1):18-25. doi: 10.1159/000215939. Epub 2009 May 6.

PMID:
19420918
31.

TGFB1 as a susceptibility gene for high myopia: a replication study with new findings.

Zha Y, Leung KH, Lo KK, Fung WY, Ng PW, Shi MG, Yap MK, Yip SP.

Arch Ophthalmol. 2009 Apr;127(4):541-8. doi: 10.1001/archophthalmol.2008.623.

PMID:
19365037
32.

De-novo identification of PPARgamma/RXR binding sites and direct targets during adipogenesis.

Hamza MS, Pott S, Vega VB, Thomsen JS, Kandhadayar GS, Ng PW, Chiu KP, Pettersson S, Wei CL, Ruan Y, Liu ET.

PLoS One. 2009;4(3):e4907. doi: 10.1371/journal.pone.0004907. Epub 2009 Mar 20.

33.

Effects of statins on the progression of cerebral white matter lesion: Post hoc analysis of the ROCAS (Regression of Cerebral Artery Stenosis) study.

Mok VC, Lam WW, Fan YH, Wong A, Ng PW, Tsoi TH, Yeung V, Wong KS.

J Neurol. 2009 May;256(5):750-7. doi: 10.1007/s00415-009-5008-7. Epub 2009 Mar 1.

PMID:
19252811
34.

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.

Pharmacogenet Genomics. 2008 Nov;18(11):989-98. doi: 10.1097/FPC.0b013e3283117d67.

PMID:
18784617
35.

LRRK2 Gly2385Arg mutation and clinical features in a Chinese population with early-onset Parkinson's disease compared to late-onset patients.

Chan DK, Ng PW, Mok V, Yeung J, Fang ZM, Clarke R, Leung E, Wong L.

J Neural Transm (Vienna). 2008 Sep;115(9):1275-7. doi: 10.1007/s00702-008-0065-0. Epub 2008 Jun 4.

PMID:
18523722
36.

The use of multiple displacement amplification to amplify complex DNA libraries.

Fullwood MJ, Tan JJ, Ng PW, Chiu KP, Liu J, Wei CL, Ruan Y.

Nucleic Acids Res. 2008 Mar;36(5):e32. doi: 10.1093/nar/gkn074. Epub 2008 Feb 19.

37.

PARK2 mutations and clinical features in a Chinese population with early-onset Parkinson's disease.

Chan DK, Mok V, Ng PW, Yeung J, Kwok JB, Fang ZM, Clarke R, Wong L, Schofield PR, Hattori N.

J Neural Transm (Vienna). 2008 May;115(5):715-9. doi: 10.1007/s00702-007-0011-6. Epub 2008 Jan 11.

PMID:
18188499
38.

Prevalence of asymptomatic intracranial atherosclerosis in high-risk patients.

Wong KS, Ng PW, Tang A, Liu R, Yeung V, Tomlinson B.

Neurology. 2007 Jun 5;68(23):2035-8.

PMID:
17548555
39.

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.

Epilepsy Behav. 2007 Aug;11(1):112-7. Epub 2007 May 22.

PMID:
17521963
40.

Linkage and association of myocilin (MYOC) polymorphisms with high myopia in a Chinese population.

Tang WC, Yip SP, Lo KK, Ng PW, Choi PS, Lee SY, Yap MK.

Mol Vis. 2007 Apr 4;13:534-44.

41.

Low-molecular-weight heparin compared with aspirin for the treatment of acute ischaemic stroke in Asian patients with large artery occlusive disease: a randomised study.

Wong KS, Chen C, Ng PW, Tsoi TH, Li HL, Fong WC, Yeung J, Wong CK, Yip KK, Gao H, Wong HB; FISS-tris Study Investigators.

Lancet Neurol. 2007 May;6(5):407-13.

PMID:
17434095
42.

The stroke epidemic.

Ng PW.

Hong Kong Med J. 2007 Apr;13(2):92-4. No abstract available.

43.

Pulsatile ocular blood flow in patients with asymmetric internal carotid artery stenosis.

Lam AK, Lam CH, Ng PW, Tsoi TH, Chan ST.

Clin Exp Optom. 2005 Nov;88(6):382-6.

44.

Impaired transcriptional upregulation of Parkin promoter variant under oxidative stress and proteasomal inhibition: clinical association.

Tan EK, Puong KY, Chan DK, Yew K, Fook-Chong S, Shen H, Ng PW, Woo J, Yuen Y, Pavanni R, Wong MC, Puvan K, Zhao Y.

Hum Genet. 2005 Dec;118(3-4):484-8. Epub 2005 Oct 22.

PMID:
16244875
45.

Prevalence and mechanism of appositional angle closure in acute primary angle closure after iridotomy.

Yeung BY, Ng PW, Chiu TY, Tsang CW, Li FC, Chi CC, Lai JS, Tham CC, Lam DS.

Clin Exp Ophthalmol. 2005 Oct;33(5):478-82.

PMID:
16181272
46.

Intermittent claudication: exercise-increased walking distance is not related to improved cardiopulmonary fitness.

Ng PW, Hollingsworth SJ, Luery H, Kumana TJ, Chaloner EJ.

Eur J Vasc Endovasc Surg. 2005 Oct;30(4):391-4.

47.

Fine needle aspiration cytology of dermatofibrosarcoma protuberans in the breast: a case report.

Tsang AK, Wong FC, Ng PW, Loke SL, Tse GM.

Pathology. 2005 Feb;37(1):84-6. No abstract available. Erratum in: Pathology. 2005 Apr;37(2):191.

PMID:
15875741
48.

Effect of MDR1 haplotype on risk of Parkinson disease.

Tan EK, Chan DK, Ng PW, Woo J, Teo YY, Tang K, Wong LP, Chong SS, Tan C, Shen H, Zhao Y, Lee CG.

Arch Neurol. 2005 Mar;62(3):460-4.

PMID:
15767512
49.

Initial viral load and the outcomes of SARS.

Chu CM, Poon LL, Cheng VC, Chan KS, Hung IF, Wong MM, Chan KH, Leung WS, Tang BS, Chan VL, Ng WL, Sim TC, Ng PW, Law KI, Tse DM, Peiris JS, Yuen KY.

CMAJ. 2004 Nov 23;171(11):1349-52.

50.

Consensus statement on ischaemic stroke care in Hong Kong.

Ng PW, Huang CY, Cheung RT, Wong KS, Wong CK, Lam JM; Hong Kong Neurological Society; Hong Kong Stroke Society.

Hong Kong Med J. 2004 Apr;10(2):124-9.

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