| Title | Author(s) | Year | View Count |  | Identifying the Service Gaps in the Management of Severe Systemic Allergic Reaction/Anaphylaxis by Paediatrics Departments of the the Hospital Authority | Ho, MHK; Wong, LM; Ling, SC; Lee, KP; Cheng, WW; Hui, J; Lau, DCY; Ng, KL; Wong, D; Kwok, KL; Kwan, EYW | 2010 | 139 |
 | An update on the epidemiology of childhood diabetes in Hong Kong | Huen, KF; Low, LCK; Cheung, PT; Wong, GWK; But, WM; Kwan, EYW; Lam, YY; Lee, CY; Wong, LM; Ng, KL; Cheng, AWF; Tong, CT; Wong, WHS | 2009 | 233 |
| A family with osteoporosis pseudoglioma syndrome due to compound heterozygosity of two novel mutations in the LRP5 gene | Cheung, WMW; Jin, LY; Smith, DK; Cheung, PT; Kwan, EYW; Low, L; Kung, AWC | 2006 | 145 |
| Aldosterone synthetase (corticosterone methyloxidase) deficiency type II in a Chinese boy | Cheung, PT; Low, LCK; Kwan, EYW | 2006 | 110 |
| 6-pyruvoyl-tetrahydropterin synthase deficiency: the clinical spectrum in 3 Chinese patients | Fung, CW; Cheung, PT; Kwan, EYW; Poon, GWK; Low, LCK; Wong, VCN | 2006 | 126 |
| Mutation analysis of the GLUT2 Gene in a Chinese patient with Fanconi-Bickel Syndrome | Poon, GWK; Kwan, EYW; Cheung, PT; Low, LCK | 2006 | 88 |
| Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria | Yuen, YP; Lam, CW; Lai, CK; Tong, SF; Li, PS; Tam, S; Kwan, EYW; Chan, SY; Tsang, WK; Chan, KY; Mak, WL; Cheng, CW; Chan, YW | 2006 | 72 |
| Family with osteoporosis Pseudolioma Syndrome due to compound heterozygosity of two novel mutations of the LRP5 gene | Jin, L; Lau, HL; Smith, DK; Lau, KS; Cheung, PT; Kwan, EYW; Low, LCK; Chan, VNY; Kung, AWC | 2005 | 103 |
| A family with osteoporosis-pseudoglioma syndrome (OPG) due to compound heterozygous mutation of the LRP5 gene | Jin, L; Lau, HL; Smith, DK; Lau, KS; Cheung, PT; Kwan, EYW; Low, LCK; Chan, VNY; Kung, AWC | 2005 | 114 |
| 6-pyruvoyl-tetrahydropterin synthase deficiency, a potentially treatable cause of dystonia | Fung, CW; Cheung, PT; Kwan, EYW; Poon, GWK; Low, LCK; Wong, VCN | 2005 | 119 |
| Prenatal Diagnosis and Prospective Management of Argininosuccinic Aciduria in the Prevention of Neonatal Hyperammonaemic Coma | Poon, GWK; Lam, CW; Tang, MHY; Wong, KY; Kwan, EYW; Cheung, PT; Low, LCK | 2004 | 132 |
| A family with osteoporosis-pseudoglioma syndrome (OPG) due to compound heterozygous mutation of the LRO5 gene | Jin, L; Lau, HL; Smith, DK; Lau, KS; Cheung, PT; Kwan, EYW; Low, LCK; Kung, AWC | 2004 | 134 |
| Robust Under the Gust – 疾 風 勁 草' | Chan, GCF; Kwan, EYW; Chiu, SY | 2004 | 152 |
| Robust Under the Gust | Chan, GCF; Kwan, EYW; Chiu, SY | 2004 | 161 |
| Antenatal Diagnosis and Postnatal Management of Tetrahydrobiopterin-deficient Hyperphenyalaninemia in a Hong Kong Chinese Infant | Lee, PPW; Poon, GWK; Kwan, EYW; Wong, KY; Chan, KW; Lee, JSK; Tam, SCF; Lau, E; Tang, MHY; Gu, XF; Low, LCK; Cheung, PT | 2004 | 104 |
| Positive Corrleation of Selective IGF-I Genotypes with Idiopathic Short Stature in Chinese Children | Man, E; Tan, KCB; Chan, KW; Yeung, LPK; Kwan, EYW; Wong, WHS; Low, LCK; Cheung, PT | 2004 | 87 |
| Mutation Analysis of the GLUT2 Gene in a Chinese Patient with Fanconi-Bickel Syndrome | Poon, GWK; Cheung, PT; Chen, RT; Kwan, EYW; Low, LCK | 2004 | 97 |
| Determinants of bone mineral density in Asian men | Gu, J; Lee, KK; Kwan, EYW; Lam, KF; Ho, AYY; Tam, S; Kung, AWC | 2004 | 110 |
| A Pilot Study of the Use of Insulin Glargine in Combination with Short Acting Insulin Analogue in Adolescents with Type I Diabetes Mellitus in Hong Kong | Au, RWM; Kwan, EYW; Yeung, LPK; Cheung, PT; Low, LCK | 2004 | 95 |
| Measles-mumps-rubella Vaccination and Egg Allergy | Chow, WC; Kwan, EYW; Lau, YL | 2003 | 112 |
|
