| Title | Author(s) | Year | View Count |
 | Malignant insulinoma with hepatoid differentiation: A unique case with alpha-fetoprotein production | Lam, KY; Lo, CY; Wat, MS; Fan, ST | 2001 | 106 |
 | Adrenal pheochromocytoma remains a frequently overlooked diagnosis | Lo, CY; Lam, KY; Wat, MS; Lam, KS | 2000 | 87 |
 | Clinical significance of Arg306 mutations of factor V gene [7] | Liang, R; Lee, CK; Wat, MS; Kwong, YL; Lam, CK; Liu, HW | 1998 | 160 |
 | Pharmacokinetics, pharmacodynamics, long-term efficacy and safety of oral 1-deamino-8-D-arginine vasopressin in adult patients with central diabetes insipidus | Lam, KSL; Wat, MS; Choi, KL; Ip, TP; Pang, RWC; Kumana, CR | 1996 | 308 |
 | Apolipoprotein (a) levels and phenotypes in NIDDM patients with microalbuminuria and albuminuria | Lam, KSL; Pang, RWC; Wat, MS; Lauder, IJ; Janus, ED | 1996 | 276 |
 | Pharmacokinetics, pharmacodynamics, long-term efficiency and safety of oral 1-deamino-8-anginine vasopressin in adult patients with central diabetes insipidus | Lam, KSL; Wat, MS; Choi, KL; Ip, TP; Kung, AWC; Kumana, CR | 1996 | 86 |
 | Clinico-pathological correlation of glucagon-positive pancreatic endocrine tumours: A presentation of five cases | Wat, MS; Lam, KY; Lam, KSL | 1995 | 100 |
 | Phaeochromocytoma associated with Myasthenia Graves' precipitated by propranolol treatment | Choi, KL; Wat, MS; Ip, TP; Kung, AWC; Lam, KSL | 1995 | 97 |
 | Aldose reductase gene polymorphism and diabetic retinopathy in NIDDM patients | Ko, CB; Lam, KSL; Chung, SSM; Wat, MS | 1995 | 75 |
 | Phaeochromocytoma associated with myasthenia gravis precipitated by propranolol treatment [1] | Choi, KL; Wat, MS; Ip, TP; Kung, AWC; Lam, KSL | 1995 | 51 |
 | Increased cholesteryl ester transfer activity in non-insulin-dependents | Tan, KCB; Lam, KSL; Wat, MS; Pang, RWC; Janus, ED | 1995 | 69 |
 | Increased cholesteryl ester transfer activity in non-insulin-dependent diabetics with and without microalbuminuria | Tan, KCB; Lam, KSL; Wat, MS; Pang, RWC; Janus, ED | 1994 | 69 |
 | Glucokinase gene mutation in a Chinese MODY family | Wat, MS; Chung, SSM; Ko, BCB; Lam, KSL | 1994 | 50 |
 | The role of polyal pathway in diabetic complications | Lee, YW; Ko, CB; Lam, KSL; Wat, MS; Chung, SK; Chung, SSM | 1994 | 100 |
 | Identification of (Pro664 -> Leu) mutation in low density lipoprotein receptor gene in Chinese patients with familial hypercholesterolaemia (Abstract) | Wong, KK; Srivastava, G; Janus, ED; Wat, MS; Lam, KSL; Ho, FCS | 1994 | 62 |
 | A case of lambert eaton myasthenic syndrome with good clinical response to 3, 4 - Diaminopyridine | Cheung, RTF; Wat, MS; Chang, PCM; Ip, MSM; Yu, YL | 1993 | 87 |
 | Childhood acute lymphoblastic leukaemia presenting with relapsing hypoplastic anaemia: Progression of the same abnormal clone | Liang, R; Cheng, G; Wat, MS; Ha, SY; Chan, LC | 1993 | 66 |
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