| Title | Author(s) | Year | View Count |  | Variable response to enzyme replacement therapy in two Chinese children with infantile-onset Pompe disease in Hong Kong | Poon, GWK; Kwok, AMK; Cheung, PT; Yung, TC; Ng, YK; Tsoi, NS; Wong, KY; Low, LCK | 2009 | 149 |
 | A rare cause of hepatosplenomegaly - transaldolase deficiency | Fung, CW; Siu, S; Mak, CM; Poon, GWK; Wong, KY; Cheung, PT; Low, LCK; Tam, S; Wong, VCN | 2007 | 120 |
| A rare cause of hepatosplenomegaly - transaldolase deficiency | Fung, CW; Siu, S; Mak, C; Poon, GWK; Cheung, PT; Low, LCK; Tam, S; Wong, VCN | 2007 | 113 |
| A rare cause of hepatosplenomegaly transaldolase deficiency | Fung, CW; Siu, S; Mak, CM; Poon, GWK; Wong, KY; Cheung, PT; Low, LCK; Tam, S; Wong, VCN | 2007 | 96 |
| Regional white matter anisotropy and general intelligence in preterm born children: a voxelwise analysis | Khong, PL; Qiu, D; Yung, AWY; Poon, GWK; Leung, C; Lam, BCC | 2006 | 74 |
| White matter volume and anisotropy in very low birth weight preterm born children: association with cognitive outcome | Khong, PL; Qiu, D; Yung, AWY; Poon, GWK; Leung, C; Chua, SE; McAlonan, GM; Lam, BCC | 2006 | 87 |
| 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 |
| White matter volume and anisotropy in preterm children: a pilot study of neurocognitive correlates | Yung, AWY; Poon, GWK; Qiu, D; Chu, J; Leung, C; Lam, BCC; Goh, WHS; Khong, PL | 2005 | 75 |
| 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 |
| Reversible Myocardial Damage in a Premature Infant with Carnitine-Acylcarnitine Translocase Deficiency | Poon, GWK; Mak, CM; Wong, RMS; Wong, KY; Yung, TC; Tam, S; Siu, STS; Lee, JSK; Low, LCK | 2004 | 107 |
| 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 |
| 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 |
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