| Title | Author(s) | Year | View Count |
 | 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 | 207 |
| Phenylketonuria in Hong Kong Chinese: A call for hyperphenylalaninemia newborn screening in the special administrative region, China | Mak, CM; Ko, CH; Lam, CW; Lau, WL; Siu, WK; Chen, SPL; Law, CY; Lai, CK; Yu, CM; Chan, AYW | 2011 | 90 |
| 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 | 233 |
| Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity | Mak, CM; Lam, CW; Tam, S; Lai, CL; Chan, LY; Fan, ST; Lau, YL; Lai, JY; Yuen, P; Hui, J; Fu, CC; Wong, KS; Mak, WL; Tze, K; Tong, SF; Lau, A; Leung, N; Hui, A; Cheung, KM; Ko, CH; Chan, YK; Ma, O; Chau, TN; Chiu, A; Chan, YW | 2008 | 211 |
| Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity (Journal of Human Genetics (2008) 53 (55-63) DOI: 10.1007/s10038-007-0218-2) | Mak, CM; Lam, CW; Tam, S; Lai, CL; Chan, LY; Fan, ST; Lau, YL; Lai, ST; Yuen, P; Hui, J; Fu, CC; Wong, KS; Mak, WL; Tze, K; Tong, SF; Lau, A; Leung, N; Hui, A; Cheung, KM; Ko, CH; Chan, YK; Ma, O; Chau, TN; Chiu, A; Chan, YW | 2008 | 76 |
 | Improving the oral health of elders in a care and attention home | Lo, ECM; Lui, KC; Au Yeung, CO; Chan, PCY; Chan, RKP; Chu, SY; Ko, CH; Lai, FWS; Li, KWK; Lin, WWS; Tse, JYY | 2005 | 114 |
 | Randomised control trial of tongue acupuncture versus sham acupuncture in improving functional outcome in cerebral palsy | Sun, JG; Ko, CH; Wong, V; Sun, XR | 2004 | 267 |
| Magnetic resonance spectroscopy and analysis of MECP2 in Rett syndrome | Khong, PL; Lam, CW; Ooi, CGC; Ko, CH; Wong, VCN | 2002 | 118 |
| Two novel CLN2 gene mutations in an Chinese patient with classical late-infantile neuronal ceroid lipofuscinosis [2] | Lam, CW; Poon, PMK; Tong, SF; Ko, CH | 2001 | 68 |
| Atypical presentation of dopa-responsive dystonia: Generalized hypotonia and proximal weakness | Kong, CK; Ko, CH; Tong, SF; Lam, CW | 2001 | 100 |
| 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 | 345 |
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