| Type | Title | Author(s) | Year | Views |
| Characteristic of patients with Duchenne Muscular Dystrophy and Becker Muscular Dystrophy in Hong KongJournal:Paediatric Neurology | Chan, SHS; Lo, IFM; Cherek, S; Cheng, WW; Fung, EI; Yeung, WL; Ngan, M; Lee, WC; Kwong, L; Wong, SN; Ma, CK; Tai, SM; Ng, SF; Wu, SP; Wong, VCN | 2014 | 21 |
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| Removing linguistic barriers to justice: a study of official reference texts for self-represented litigants in Hong KongJournal:Meta: Translator’s Journal | Yeung, WL; Leung, JHC | 2013 | 75 |
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| A territory wide study for dystrophinopathy in Hong KongProceedings/Conference:Neuromuscular Disorders Publisher:Elsevier Ltd. The Journal's web site is located at http://www.elsevier.com/locate/nmd | Chan, SHS; Lo, IFM; Cherk, S; Cheng, WWS; Fung, E; Yeung, WL; Lee, WC; Wong, S; Ma, CKL; Tai, SM; Yau, MM; Ng, G; Wu, SP; Wong, VCN | 2013 | 25 |
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| Removing linguistic barriers to justice: a study of official reference texts for unrepresented litigantsProceedings/Conference:2nd International Conference on Law, Language and Discourse, LLD2 | Yeung, WL; Leung, JHC | 2012 | 59 |
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| Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiencyJournal:Journal of Child Neurology Publisher:Sage Publications, Inc.. The Journal's web site is located at http://jcn.sagepub.com | Yeung, WL; Wong, VCN; Chan, KY; Hui, J; Fung, CW; Yau, E; Ko, CH; Lam, CW; Mak, CM; Siu, S; Low, L | 2011 | 266 |
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| Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong ChineseJournal:Molecular Genetics and Metabolism Publisher:Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/ymgme | Mak, CM; Lam, CW; Siu, TS; Chan, KY; Siu, WK; Yeung, WL; Hui, J; Wong, VCN; Low, LCK; Ko, CH; Fung, CW; Chen, SP; Yuen, YP; Lee, HC; Yau, E; Chan, B; Tong, SF; Tam, S; Chan, YW | 2010 | 275 |
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| Intra-familial variation in clinical manifestations and response to ephedrine in siblings with congenital myasthenic syndrome caused by novel COLQ mutationsJournal:Developmental Medicine and Child Neurology Publisher:Mac Keith Press. The Journal's web site is located at http://www.mackeith.co.uk/journal.html | Yeung, WL; Lam, CW; Ng, PC | 2010 | 178 |
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| Severe congenital myasthenia gravis of the presynaptic type with choline acetyltransferase mutation in a Chinese infant with respiratory failurePublisher:S Karger AG. The Journal's web site is located at http://www.karger.com/BON | Yeung, WL; Lam, CW; Fung, LWE; Hon, KLE; Ng, PC | 2009 | 173 |
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| Galactorrhea-A strong clinical clue towards the diagnosis of neurotransmitter diseaseJournal:Brain and Development Publisher:Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/braindev | Yeung, WL; Lam, CW; Hui, J; Tong, SF; Wu, SP | 2006 | 103 |
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| Early-onset primary torsional dystonia in a 4-generation Chinese family with a mutation in the DYT1 geneJournal:Chinese Medical Journal Publisher:Zhonghua Yixuehui. The Journal's web site is located at http://www.cmj.org/ | Yeung, WL; Lam, CW; Cheng, WT; Sin, NC; Wong, WK; Wong, CN; Tse, KM; Fok, TF | 2005 | 112 |
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| Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.Journal:Journal of medical genetics Publisher:B M J Publishing Group. The Journal's web site is located at http://jmg.bmjjournals.com/ | Lam, CW; Yeung, WL; Ko, CH; Poon, PM; Tong, SF; Chan, KY; Lo, IF; Chan, LY; Hui, J; Wong, V; Pang, CP; Lo, YM; Fok, TF | 2000 | 360 |
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