| Type | Title | Author(s) | Year | Views |
| Review of evolution of clinical, training and educational services and research program for autism spectrum disorders in Hong Kong. | Wong, VCN; Fung, CW; Lee, SL | 2012 | 132 |
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| COG5-CDG with a Mild Neurohepatic Presentation | Fung, CW; Matthijs, G; Sturiale, L; garozzo, D; Wong, KY; Wong, RMS; Wong, VCN; Jaeken, J | 2012 | 100 |
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| Dravet Syndrome-Genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children. | Wong, VCN; Kwong, KY; Fung, CW | 2012 | 92 |
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| Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong | Fung, CW; Smeitenk, J; Rodenburg, R; Siu, S; Ma, O; Poon, G; Tam, S; Wong, V | 2012 | 75 |
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| Dravet syndrome - genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children | Wong, V; Kwong, A; Fung, CW | 2012 | 95 |
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| Paroxysmal non-epileptic movements in childhood | Fung, CW; Wong, VCN | 2012 | 86 |
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| Arginase deficiency with new phenotype and a novel mutation: Contemporary Summary | Tsang, JPK; Poon, WL; Luk, HM; Fung, CW; Ching, CK; Mak, CM; Lam, CW; Siu, TS; Tam, S; Wong, VCN | 2012 | 29 |
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| Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome | Kwong, AKY; Fung, CW; Chan, SY; Wong, VCN | 2012 | 101 |
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| Dravet syndeome: genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children | Wong, VCN; Kwong, A; Fung, CW | 2012 | 21 |
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| Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiency | Yeung, WL; Wong, VCN; Chan, KY; Hui, J; Fung, CW; Yau, E; Ko, CH; Lam, CW; Mak, CM; Siu, S; Low, L | 2011 | 258 |
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| Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong (poster) | Wong, VCN; Fung, CW | 2011 | 76 |
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| A study of cerebrospinal fluid neurotransmitters assay in children with undiagnosed neurological diseases in Hong Kong | Fung, CW; Poon, G; Kwok, A; Cheung, PT; Low, L; Blau, N; Siu, S; Mak, C; Tam, S; Wong, V | 2010 | 145 |
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| Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong | Fung, CW; Poon, G; Kwok, A; Cheung, PT; Low, L; Mak, C; Tam, S; Siu, S; Wong, V | 2010 | 189 |
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| Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese | Mak, CM; Lam, CW; Siu, TS; Chan, KY; Siu, WK; Yeung, WL; Hui, J; Wong, VCN; Low, LCK; Ko, CH; Fung, CW; Chen, SP; Yuen, YP; Lee, HC; Yau, E; Chan, B; Tong, SF; Tam, S; Chan, YW | 2010 | 267 |
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| Anti-NMDA receptor encephalitis with atypical brain changes on MRI | Chan, SHS; Wong, VCN; Fung, CW; Dale, RC; Vincent, A | 2010 | 169 |
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| Kbg syndrome: Clinical features and specific dental findings | Almandey, HA; Anthonappa, RP; King, NM; Fung, CW | 2010 | 164 |
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| Clinical profile of 13 children with severe myoclonic epilepsy of infancy in Hong Kong | Fung, CW; Wong, VCN | 2010 | 90 |
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| Anti-NMDA-R encephalitis: an encephalitis lerthargica-like illness | Chan, SHS; Fung, CW; Yung, AWY; Lee, SL; Wong, VCN; Dale, RC; Vincent, A | 2009 | 167 |
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| A study of cerebrospinal fluid neurotransmitters assay in children with undiagnosed neurological diseases in Hong Kong | Fung, CW; Siu, S; Poon, G; Kwok, A; Cheung, PT; Low, L; Mak, C; Tam, S; Wong, VCN | 2009 | 341 |
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| Infantile Convulsion Choreoathetosis Syndrome in a Hong Kong Chinese Family | Fung, CW; Chung, BHY; Ng, P; Zhao, M; Yang, W; Wong, VCN | 2009 | 171 |
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