| Title | Author(s) | Year | View Count |  | Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3 | Cheung, CL; Lau, KS; Ho, AYY; Lee, KK; Tiu, SC; Lau, EYF; Leung, J; Tsang, MW; Chan, KW; Yeung, CY; Woo, YC; Cheung, EYN; Hung, VHF; Pang, HK; Hung, CS; Sham, PC; Kung, AWC | 2012 | 62 |
| Circulating fluorocytes at the first attack of acute intermittent porphyria: A missing link in the pathogenesis | Lam, CW; Lau, KC; Mak, CM; Tsang, MW; Chan, YW | 2011 | 196 |
| Engineered Amp C β-lactamase as a fluorescent screening tool for class C β-lactamase inhibitors | Tsang, MW; Chan, PH; So, PK; Ma, DL; Tsang, CW; Wong, KY; Leung, YC | 2011 | 60 |
| Genetic and clinical characteristics of maturity-onset diabetes of the young in Chinese patients | Xu, JY; Dan, QH; Chan, V; Wat, NMS; Tam, S; Tiu, SC; Lee, KF; Siu, SC; Tsang, MW; Fung, LM; Chan, KW; Lam, KSL | 2005 | 125 |
 | Genetic and clinical characteristics of maturity-onset diabetes of the young in Chinese patient | Xu, J; Dan, Q; Chan, VNY; Wat, NMS; Tam, S; Tiu, SC; Lee, KF; Siu, SC; Tsang, MW; Fung, LM; Chan, KW; Lam, KSL | 2004 | 100 |
| Regulation of epididymal principal cell functions by basal cells: Role of transient receptor potential (Trp) proteins and cyclooxygenase-1 (COX-1) | Leung, GPH; Cheung, KH; Leung, CT; Tsang, MW; Wong, PYD | 2004 | 46 |
| Pathogenic mutations of the lipoprotein lipase gene in Chinese patients with hypertriglyceridemic type 2 diabetes. | Yang, T; Pang, CP; Tsang, MW; Lam, CW; Poon, PM; Chan, LY; Wu, XQ; Tomlinson, B; Baum, L | 2003 | 87 |
| Mutation-function analysis in the lipoprotein lipase gene of Chinese patients with hypertriglyceridemic type 2 diabetes | Yang, T; Lam, CW; Tsang, MW; Chan, LY; Poon, PM; Huang, SZ; Pang, CP | 2003 | 102 |
| Genotype-phenotype studies of six novel LPL mutations in Chinese patients with hypertriglyceridemia. | Chan, LY; Lam, CW; Mak, YT; Tomlinson, B; Tsang, MW; Baum, L; Masarei, JR; Pang, CP | 2002 | 89 |
| Homoplasmic 3316G-->A in the ND1 gene of the mitochondrial genome: a pathogenic mutation or a neutral polymorphism? | Lam, CW; Yang, T; Tsang, MW; Pang, CP | 2001 | 51 |
| Novel single nucleotide polymorphisms (3203A>G and 3204C>T) in the 3' end of the mitochondrial 16S rRNA gene. | Yang, T; Lam, CW; Tsang, MW; Tong, SF; Chan, LY; Kam, GY; Poon, PM; Wu, XQ; Pang, CP | 2000 | 54 |
 | Acarbose in NIDDM patients with poor control on conventional oral agents: A 24-week placebo-controlled study | Lam, KSL; Tiu, SC; Tsang, MW; Ip, TP; Tam, SCF | 1998 | 366 |
| An open multicentre study evaluating the use of Novopenr3 for insulin requiring diabetic patients. | So, TMY; Jorgensen, LN; Lam, KSL; Cockram, CS; Cheung, KO; Lau, IT; Lo, KW; Siu, SC; Tiu, SC; Tsang, MW | 1996 | 83 |
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