Results 1 to 20 of 52
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TypeTitleAuthor(s)YearViews
Arginase deficiency with new phenotype and a novel mutation: Contemporary SummaryTsang, JPK; Poon, WL; Luk, HM; Fung, CW; Ching, CK; Mak, CM; Lam, CW; Siu, TS; Tam, S; Wong, VCN201243
 
Dravet Syndrome-Genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children.Wong, VCN; Kwong, KY; Fung, CW201271
 
COG5-CDG with a Mild Neurohepatic PresentationFung, CW; Matthijs, G; Sturiale, L; garozzo, D; Wong, KY; Wong, RMS; Wong, VCN; Jaeken, J201291
 
Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndromeKwong, AKY; Fung, CW; Chan, SY; Wong, VCN201296
 
Review of evolution of clinical, training and educational services and research program for autism spectrum disorders in Hong Kong.Wong, VCN; Fung, CW; Lee, SL2012101
 
Dravet syndeome: genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese childrenWong, VCN; Kwong, A; Fung, CW201229
 
Dravet syndrome - genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese childrenWong, V; Kwong, A; Fung, CW201275
 
Paroxysmal non-epileptic movements in childhoodFung, CW; Wong, VCN201277
 
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong KongFung, CW; Smeitenk, J; Rodenburg, R; Siu, S; Ma, O; Poon, G; Tam, S; Wong, V201274
 
Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiencyYeung, WL; Wong, VCN; Chan, KY; Hui, J; Fung, CW; Yau, E; Ko, CH; Lam, CW; Mak, CM; Siu, S; Low, L2011221
 
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong (poster)Wong, VCN; Fung, CW201154
 
Clinical profile of 13 children with severe myoclonic epilepsy of infancy in Hong KongFung, CW; Wong, VCN201063
 
Kbg syndrome: Clinical features and specific dental findingsAlmandey, HA; Anthonappa, RP; King, NM; Fung, CW2010136
 
Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong ChineseMak, 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, YW2010242
 
Anti-NMDA receptor encephalitis with atypical brain changes on MRIChan, SHS; Wong, VCN; Fung, CW; Dale, RC; Vincent, A2010125
 
A study of cerebrospinal fluid neurotransmitters assay in children with undiagnosed neurological diseases in Hong KongFung, CW; Poon, G; Kwok, A; Cheung, PT; Low, L; Blau, N; Siu, S; Mak, C; Tam, S; Wong, V2010120
 
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong KongFung, CW; Poon, G; Kwok, A; Cheung, PT; Low, L; Mak, C; Tam, S; Siu, S; Wong, V2010142
 
Infantile Convulsion Choreoathetosis Syndrome in a Hong Kong Chinese FamilyFung, CW; Chung, BHY; Ng, P; Zhao, M; Yang, W; Wong, VCN2009128
 
Anti-NMDA-R encephalitis: an encephalitis lerthargica-like illnessChan, SHS; Fung, CW; Yung, AWY; Lee, SL; Wong, VCN; Dale, RC; Vincent, A2009152
 
A study of cerebrospinal fluid neurotransmitters assay in children with undiagnosed neurological diseases in Hong KongFung, CW; Siu, S; Poon, G; Kwok, A; Cheung, PT; Low, L; Mak, C; Tam, S; Wong, VCN2009297
 
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