| Type | Title | Author(s) | Year | Views |
| Folinic acid responsive epilepsy in Ohtahara Syndrome caused by STXBP1 mutationJournal:Pediatric Neurology | Tso, WYW; Kwong, AK; Fung, CW; Wong, VCN | 2014 | 21 |
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| Lathosterolosis: A Disorder Of Cholesterol Biosynthesis Resembling Smith-lemli-opitz SyndromeJournal:Journal Of Inherited Metabolic Disease | Ho, CCA; Fung, CW; Siu, TS; Ma, OCK; Lam, CW; Tam, S; Wong, VCN | 2014 | 20 |
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| Clinical And Genetic Evaluation Of 23 Children With Infantile Onset Epileptic Encephalopathy (iee)Proceedings/Conference:The 3rd Hong Kong Neurological Congress Cum 26th Annual Scientific Meeting Of The Hong Kong Neurological Society. 2-3 November, 2013 | Ho, CCA; Kwong, KY; Fung, CW; Wong, VCN | 2013 | 10 |
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| Folinic acid responsive epilepsy in Ohtahara syndrome caused by STXBP1 mutation.Journal:Pediatric Neurology | Tso, WWY; Kwong, KY; Wong, VCN; Fung, CW | 2013 | 1 |
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| Arginase deficiency with new phenotype and a novel mutation: Contemporary SummaryJournal:Pediatric Neurology | Tsang, JPK; Poon, WL; Luk, HM; Fung, CW; Ching, CK; Mak, CM; Lam, CW; Siu, TS; Tam, S; Wong, VCN | 2012 | 68 |
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| Dravet Syndrome-Genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children.Proceedings/Conference:International Meeting for Autism Research, Toronto, Ontario, Canada, 17-19 May | Wong, VCN; Kwong, KY; Fung, CW | 2012 | 88 |
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| COG5-CDG with a Mild Neurohepatic PresentationPublisher:SSIEM and Springer-verlag Berlin Heidelberg. | Fung, CW; Matthijs, G; Sturiale, L; garozzo, D; Wong, KY; Wong, RMS; Wong, VCN; Jaeken, J | 2012 | 110 |
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| Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndromePublisher:Public Library of Science. The Journal's web site is located at http://www.plosone.org/home.action | Kwong, AKY; Fung, CW; Chan, SY; Wong, VCN | 2012 | 134 |
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| Dravet syndeome: genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese childrenProceedings/Conference:Hong Kong Medical Journal Publisher:Hong Kong Academy of Medicine Press. The Journal's web site is located at http://www.hkmj.org.hk | Wong, VCN; Kwong, A; Fung, CW | 2012 | 42 |
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| Dravet syndrome - genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese childrenProceedings/Conference:Developmental Medicine and Child Neurology Publisher:Mac Keith Press. The Journal's web site is located at http://www.mackeith.co.uk/journal.html | Wong, V; Kwong, A; Fung, CW | 2012 | 97 |
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| Paroxysmal non-epileptic movements in childhoodJournal:HK Journal of Paediatrics (new series) | Fung, CW; Wong, VCN | 2012 | 93 |
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| Spectrum of mitochondrial diseases in a tertiary referral centre in Hong KongProceedings/Conference:Developmental Medicine and Child Neurology Publisher:Mac Keith Press. The Journal's web site is located at http://www.mackeith.co.uk/journal.html | Fung, CW; Smeitenk, J; Rodenburg, R; Siu, S; Ma, O; Poon, G; Tam, S; Wong, V | 2012 | 111 |
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| Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiencyJournal:Journal of Child Neurology Publisher:Sage Publications, Inc.. The Journal's web site is located at http://jcn.sagepub.com | Yeung, WL; Wong, VCN; Chan, KY; Hui, J; Fung, CW; Yau, E; Ko, CH; Lam, CW; Mak, CM; Siu, S; Low, L | 2011 | 266 |
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| Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong (poster)Proceedings/Conference:Hospital Authority Convention 2011, Hong Kong | Wong, VCN; Fung, CW | 2011 | 68 |
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| Clinical profile of 13 children with severe myoclonic epilepsy of infancy in Hong KongProceedings/Conference:Asian & Oceanian Epilepsy Congress | Fung, CW; Wong, VCN | 2010 | 74 |
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| Kbg syndrome: Clinical features and specific dental findingsJournal:Pediatric Dentistry Publisher:American Academy of Pediatric Dentistry. The Journal's web site is located at http://www.aapd.org/publications/peddent/ | Almandey, HA; Anthonappa, RP; King, NM; Fung, CW | 2010 | 160 |
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| Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong ChineseJournal:Molecular Genetics and Metabolism Publisher:Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/ymgme | 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 | 275 |
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| Anti-NMDA receptor encephalitis with atypical brain changes on MRIJournal:Pediatric Neurology Publisher:Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/pedneu | Chan, SHS; Wong, VCN; Fung, CW; Dale, RC; Vincent, A | 2010 | 154 |
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| A study of cerebrospinal fluid neurotransmitters assay in children with undiagnosed neurological diseases in Hong KongProceedings/Conference:Proceedings of the International Symposium on Epilepsy in Neurometabolic Diseases | Fung, CW; Poon, G; Kwok, A; Cheung, PT; Low, L; Blau, N; Siu, S; Mak, C; Tam, S; Wong, V | 2010 | 160 |
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| Spectrum of mitochondrial diseases in a tertiary referral centre in Hong KongProceedings/Conference:International Symposium on Epilepsy in Neurometabolic Diseases, ISENMD 2010 | Fung, CW; Poon, G; Kwok, A; Cheung, PT; Low, L; Mak, C; Tam, S; Siu, S; Wong, V | 2010 | 178 |
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