Browsing by Author Poon, GWK

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Showing results 1 to 14 of 14
TitleAuthor(s)Issue DateViews
 
6-pyruvoyl-tetrahydropterin synthase deficiency, a potentially treatable cause of dystonia
Proceeding/Conference:50th Anniversary Symposium on Paediatric Neurology & Neuro-rehabilitation
2005
72
2006
83
 
2004
90
 
Mutation analysis of the GLUT2 Gene in a Chinese Patient with Fanconi-Bickel Syndrome
Proceeding/Conference:Hong Kong Journal of Paediatrics (New Series)
2004
59
 
Mutation analysis of the GLUT2 Gene in a Chinese patient with Fanconi-Bickel Syndrome
Proceeding/Conference:Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society, APPES 2006
2006
45
 
2004
63
 
A rare cause of hepatosplenomegaly - transaldolase deficiency
Proceeding/Conference:Annual Symposium of Society for the Study of Inborn Errors of Metabolism, SSIEM 2007
2007
75
A rare cause of hepatosplenomegaly - transaldolase deficiency
Proceeding/Conference:Journal of Inherited Metabolic Disease
2007
1330
 
A rare cause of hepatosplenomegaly transaldolase deficiency
Proceeding/Conference:Joint Annual Scientific Meeting for Paediatricians & Paediatric Nurses
2007
84
 
Regional white matter anisotropy and general intelligence in preterm born children: a voxelwise analysis
Proceeding/Conference:Proceedings of The International Society for Magnetic Resonance in Medicine
2006
29
 
2004
56
 
2009
82
 
White matter volume and anisotropy in preterm children: a pilot study of neurocognitive correlates
Proceeding/Conference:Annual Congress of Asian Society for Pediatric Research
2005
40
 
2006
50