Results 1 to 14 of 14
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TypeTitleAuthor(s)YearViews
Variable response to enzyme replacement therapy in two Chinese children with infantile-onset Pompe disease in Hong KongPoon, GWK; Kwok, AMK; Cheung, PT; Yung, TC; Ng, YK; Tsoi, NS; Wong, KY; Low, LCK2009124
 
A rare cause of hepatosplenomegaly - transaldolase deficiencyFung, CW; Siu, S; Mak, CM; Poon, GWK; Wong, KY; Cheung, PT; Low, LCK; Tam, S; Wong, VCN2007141
 
A rare cause of hepatosplenomegaly - transaldolase deficiencyFung, CW; Siu, S; Mak, C; Poon, GWK; Cheung, PT; Low, LCK; Tam, S; Wong, VCN200798
 
A rare cause of hepatosplenomegaly transaldolase deficiencyFung, CW; Siu, S; Mak, CM; Poon, GWK; Wong, KY; Cheung, PT; Low, LCK; Tam, S; Wong, VCN200798
 
Regional white matter anisotropy and general intelligence in preterm born children: a voxelwise analysisKhong, PL; Qiu, D; Yung, AWY; Poon, GWK; Leung, C; Lam, BCC200662
 
White matter volume and anisotropy in very low birth weight preterm born children: association with cognitive outcomeKhong, PL; Qiu, D; Yung, AWY; Poon, GWK; Leung, C; Chua, SE; McAlonan, GM; Lam, BCC200664
 
Mutation analysis of the GLUT2 Gene in a Chinese patient with Fanconi-Bickel SyndromePoon, GWK; Kwan, EYW; Cheung, PT; Low, LCK200673
 
6-pyruvoyl-tetrahydropterin synthase deficiency: the clinical spectrum in 3 Chinese patientsFung, CW; Cheung, PT; Kwan, EYW; Poon, GWK; Low, LCK; Wong, VCN2006115
 
White matter volume and anisotropy in preterm children: a pilot study of neurocognitive correlatesYung, AWY; Poon, GWK; Qiu, D; Chu, J; Leung, C; Lam, BCC; Goh, WHS; Khong, PL200569
 
6-pyruvoyl-tetrahydropterin synthase deficiency, a potentially treatable cause of dystoniaFung, CW; Cheung, PT; Kwan, EYW; Poon, GWK; Low, LCK; Wong, VCN2005122
 
Prenatal Diagnosis and Prospective Management of Argininosuccinic Aciduria in the Prevention of Neonatal Hyperammonaemic ComaPoon, GWK; Lam, CW; Tang, MHY; Wong, KY; Kwan, EYW; Cheung, PT; Low, LCK2004108
 
Reversible Myocardial Damage in a Premature Infant with Carnitine-Acylcarnitine Translocase DeficiencyPoon, GWK; Mak, CM; Wong, RMS; Wong, KY; Yung, TC; Tam, S; Siu, STS; Lee, JSK; Low, LCK2004103
 
Antenatal Diagnosis and Postnatal Management of Tetrahydrobiopterin-deficient Hyperphenyalaninemia in a Hong Kong Chinese InfantLee, PPW; Poon, GWK; Kwan, EYW; Wong, KY; Chan, KW; Lee, JSK; Tam, SCF; Lau, E; Tang, MHY; Gu, XF; Low, LCK; Cheung, PT2004113
 
Mutation Analysis of the GLUT2 Gene in a Chinese Patient with Fanconi-Bickel SyndromePoon, GWK; Cheung, PT; Chen, RT; Kwan, EYW; Low, LCK200479
 
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