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Title	Author(s)	Issue Date	Views
6-pyruvoyl-tetrahydropterin synthase deficiency, a potentially treatable cause of dystonia Proceeding/Conference:50th Anniversary Symposium on Paediatric Neurology & Neuro-rehabilitation	Fung, CW Cheung, PT Kwan, EYW Poon, GWK Low, LCK Wong, VCN	2005	62
6-pyruvoyl-tetrahydropterin synthase deficiency: the clinical spectrum in 3 Chinese patients Proceeding/Conference:Neuropediatrics	Fung, CW Cheung, PT Kwan, EYW Poon, GWK Low, LCK Wong, VCN	2006	63
A simple blood test expedites the diagnosis of GLUT1 deficiency syndrome Journal:Annals of Neurology	Gras, D Cousin, C Kappeler, C Fung, CW Auvin, S Essid, N Chung, BHY Dacosta, L Hainque, E Luton, M Petit, V Vuillaumier, S Tanguy, OB Flamand-roze, E Mochel, F	2017	21
Analysis of mutations in 7 genes associated with neuronal excitability and synaptic transmission in a cohort of children with non-syndromic Infantile Epileptic Encephalopathy Journal:PLoS One	Kwong, AKY Ho, CCA Fung, CW Wong, VCN	2015	33
Anti-NMDA receptor encephalitis with atypical brain changes on MRI Journal:Pediatric Neurology	Chan, SHS Wong, VCN Fung, CW Dale, RC Vincent, A	2010	73
Anti-NMDA-R encephalitis: an encephalitis lerthargica-like illness Proceeding/Conference:Hong Kong Medical Journal	Chan, SHS Fung, CW Yung, AWY Lee, SL Wong, VCN Dale, RC Vincent, A	2009	93
Anti-NMDAR encephalitis: An encephalitis lethargica like illness Proceeding/Conference:International Child Neurology Congress (ICNC)	Chan, SHS Wong, VCN Fung, CW Dale, RC Vincent, A Yung, AWY Lee, SL	2010	42
Arginase deficiency with new phenotype and a novel mutation: Contemporary Summary Journal:Pediatric Neurology	Tsang, JPK Poon, WL Luk, HM Fung, CW Ching, CK Mak, CM Lam, CW Siu, TS Tam, S Wong, VCN	2012	46
Avoidance of Left Ventricularof Dyssnchrony Detected by Tissue Doppler Echocardiography by Permanent Right Ventricular Septal Pacing in Patients with High-Grade atrioventricular block Proceeding/Conference:Journal of the American College of Cardiology	Tse, HF Lam, YM Tang, MO Tsang, V Fung, CW Lau, CP	2006	59
Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese Journal:Molecular Genetics and Metabolism	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	165
Children with mesial temporal sclerosis (MTS) in an epilepsy cohort - a different clinical spectrum? Proceeding/Conference:50th Anniversary Symposium on Paediatric Neurology & Neuro-Rehabilitation	Fung, CW Wong, VCN	2005	7
Clinical and genetic evaluation of 23 children with infantile onset epileptic encephalopathy Proceeding/Conference:Hong Kong Medical Journal	Ho, ACC Kwong, AKY Fung, CW Wong, VCN	2013	34
Clinical profile of 13 children with severe myoclonic epilepsy of infancy in Hong Kong Proceeding/Conference:Asian & Oceanian Epilepsy Congress, AOEC 2010	Fung, CW Wong, VCN	2010	31
The clinical utility of radiologic screening in asymptomatic neurofibromatosis-1 (NF-1) Proceeding/Conference:Annual Meeting of the Society for Pediatric Radiology, SPR 2002	Khong, PL Goh, WHS Wong, VCN Fung, CW Ooi, CGC	2002	50
COG5-CDG with a Mild Neurohepatic Presentation Journal:JIMD Reports	Fung, CW Matthijs, G Sturiale, L garozzo, D Wong, KY Wong, RMS Wong, VCN Jaeken, J	2012	80
Comprehensive Paediatric Epilepsy Program in Hong Kong West Cluster: Queen Mary Hospital/Duchess of Kent Children's Hospital - Development of Paediatric Epilepsy Surgery Program 1997-2007 Proceeding/Conference:National Child Neurology Congress	Yung, AWY Hung, KN Khong, PL Ho, WY Fung, CW Leung, CSY Fan, YW Wong, VCN	2007	61
Copy number variation in Hong Kong patients with autism spectrum disorder Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)	Mak, ASL Leung, GKC Mak, CCY Chu, YWY Mok, GTK Tang, TWF Chan, KYK Kan, ASY Tang, MHY Lau, ETK So, KW Tao, QV Fung, CW Wong, VCN Lee, SL Chung, BHY	2016	68
COQ10 deficiency due to biallelic COQ4 mutations – An early onset mitochondrial disorder common in southern Chinese due to a founder mutation Proceeding/Conference:2nd Joint Annual Research & Scientific Meeting 2018 of the Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association and Hong Kong College of Paediatric Nursing	YU, HC TSANG, HY Pei, LCS Chan, VCM Rodenburg, RJT Smeitink, J Lee, NNC Fung, CW Chung, BHY	2018	7
Demonstration of nitric oxide generation during renal ischemia-reperfusion injury Proceeding/Conference:Transplantation Proceedings	Lui, SL Zhang, XH Zhu, W Lo, CY Chan, DTM Fung, CW Lai, KN	1999	38
Demonstration of nitric oxide generation during renal ischemia-reperfusion injury using paramagnetic resonnance spectroscopy Journal:Transplantation Proceedings	Lui, SL Zhang, XH Zhu, W Lo, CY Chan, DTM Fung, CW Lai, KN	1999	42

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