| Title | Author(s) | Year | View Count |
 | Mutation origin of Machado-Joseph Disease in the Australian Aboriginal Communities of Groote Eylandt and Yirrkala | Martins, S; Soong, BW; Wong, VCN; Giunti, P; Stevanin, G; Ranum, LPW; Sasaki, H; Riess, O; Tsuji, S; Countinho, P; Amorim, A; Sequeiros, J; Nicholson, GA | 2012 | 74 |
| COG5-CDG with a Mild Neurohepatic Presentation | Fung, CW; Matthijs, G; Sturiale, L; garozzo, D; Wong, KY; Wong, RMS; Wong, VCN; Jaeken, J | 2012 | 71 |
| 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 | 86 |
| Klein Levin Syndrome is a steroid-responsive, non NMDA receptor-mediated encephalitis (poster presentation) | Wong, S; Cheung, P; Wong, VCN; Ma, L; Chan, B | 2012 | 73 |
 | Autism spectrum conditions: FAQs on Autism, Asperger Syndrome and Atypical Autism answered by international experts | Wong, V | 2012 | 147 |
| Acupuncture for acute management and rehabilitation of traumatic brain injury | Wong, V; Cheuk, DKL; Lee, S; Chu, V | 2012 | 56 |
| Paroxysmal non-epileptic movements in childhood | Fung, CW; Wong, VCN | 2012 | 60 |
| 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 | 46 |
| Klein Levin Syndrome is a steriod-responsive, non-N-methyl-D-aspartate receptor-mediated encephalitis | Wong, S; Cheung, P; Wong, VCN; Chan, B | 2012 | 69 |
 | Pilot study for subgroup classification for autism spectrum disorder based on dysmorphology and physical measurements in Chinese children | Wong, PTY; Wong, VCN | 2012 | 58 |
| Pilot study for subgroup classification for autism spectrum disorder based on dysmorphology and physical measurements in Chinese children | Wong, V; Wong, P | 2012 | 53 |
| Dravet syndrome - genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children | Wong, V; Kwong, A; Fung, CW | 2012 | 51 |
| Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome | Kwong, AKY; Fung, CW; Chan, SY; Wong, VCN | 2012 | 59 |
| Dravet Syndrome-Genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children. | Wong, VCN; Kwong, KY; Fung, CW | 2012 | 58 |
| Spinal muscular atrophy in Chinese | Chan, VNY; Wong, VCN | 2012 | 35 |
| Diarrhea: Case definition and guidelines for collection, analysis, and presentation of immunization safety data | Gidudu, J; Sack, DA; Pina, M; Hudson, MJ; Kohl, KS; Bishop, P; Chatterjee, A; Chiappini, E; Compingbutra, A; Da Costa, C; Fernandopulle, R; Fischer, TK; Haber, P; Masana, W; De Menezes, MR; Kang, G; KhuriBulos, N; Killion, LA; Nair, C; Poerschke, G; Rath, B; SalazarLindo, E; Setse, R; Wenger, P; Wong, VCN; Zaman, K | 2011 | 45 |
| Gene-wide tagging study of the association between ABCC2, ABCC5 and ABCG2 genetic polymorphisms and multidrug resistance in epilepsy | Kwan, P; Wong, V; Ng, PW; Lui, CHT; Sin, NC; Wong, KS; Baum, L | 2011 | 45 |
| Value of clinical assessment in the diagnostic evaluation of Global Developmental Delay (GDD) using a Likelihood Ratio Model | Wong, VCN; Chung, B | 2011 | 270 |
| Possible effect of acupuncture in autism spectrum disorder | Rose, L; Wong, VCN | 2011 | 127 |
| 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 | 206 |
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