| Title | Author(s) | Year | View Count |
 | Removing linguistic barriers to justice: a study of official reference texts for self-represented litigants in Hong Kong | Yeung, WL; Leung, JHC | 2013 | 44 |
| Removing linguistic barriers to justice: a study of official reference texts for unrepresented litigants | Yeung, WL; Leung, JHC | 2012 | 31 |
 | Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiency | Yeung, WL; Wong, VCN; Chan, KY; Hui, J; Fung, CW; Yau, E; Ko, CH; Lam, CW; Mak, CM; Siu, S; Low, L | 2011 | 208 |
| 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, VCN; Low, LCK; Ko, CH; Fung, CW; Chen, SP; Yuen, YP; Lee, HC; Yau, E; Chan, B; Tong, SF; Tam, S; Chan, YW | 2010 | 236 |
| Intra-familial variation in clinical manifestations and response to ephedrine in siblings with congenital myasthenic syndrome caused by novel COLQ mutations | Yeung, WL; Lam, CW; Ng, PC | 2010 | 155 |
| Severe congenital myasthenia gravis of the presynaptic type with choline acetyltransferase mutation in a Chinese infant with respiratory failure | Yeung, WL; Lam, CW; Fung, LWE; Hon, KLE; Ng, PC | 2009 | 98 |
| Galactorrhea-A strong clinical clue towards the diagnosis of neurotransmitter disease | Yeung, WL; Lam, CW; Hui, J; Tong, SF; Wu, SP | 2006 | 59 |
| Early-onset primary torsional dystonia in a 4-generation Chinese family with a mutation in the DYT1 gene | Yeung, WL; Lam, CW; Cheng, WT; Sin, NC; Wong, WK; Wong, CN; Tse, KM; Fok, TF | 2005 | 75 |
 | Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome. | 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 | 347 |
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