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Showing results 13 to 32 of 97 < previous next >

Title	Author(s)	Issue Date	Views
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	261
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	23
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
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
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	98
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	251
Comprehensive genetic evaluation in paediatric-onset mitochondrial diseases Proceeding/Conference:Joint Annual Scientific Meeting 2019 of The Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association, & Hong Kong College of Paediatric Nursing	Tsang, MHY Kwong, AKY Fung, JLF Yu, MHC Yeung, KS Mak, CCY Rodenburg, R Smeitink, J Luk, HM Lo, FMI Chung, BHY Fung, CW	2019
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
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	100
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	58
Delineation of molecular findings by whole-exome sequencing for suspected cases of paediatric-onset mitochondrial diseases in the Southern Chinese population Journal:Human Genomics	TSANG, MHY Kwong, AKY Chan, KLS Fung, JLF YU, MHC Mak, CCY Yeung, KS Rodenburg, RJT Smeitink, JAM Chan, R Tsoi, T Hui, J Wong, SSN Tai, SM Chan, VCM Ma, CK Fung, STH Wu, SP Chak, WK Chung, BHY Fung, CW	2020	24
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
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
A diagrammatic approach to search for minimum sampling frequency and quantization resolution for digital control of power converters Proceeding/Conference:PESC Record - IEEE Annual Power Electronics Specialists Conference	Fung, CW Liu, CP Pong, MH	2007	183
Dravet syndeome: genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children Proceeding/Conference:Hong Kong Medical Journal	Wong, VCN Kwong, A Fung, CW	2012
Dravet syndrome - genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children Proceeding/Conference:Developmental Medicine and Child Neurology	Wong, V Kwong, A Fung, CW	2012	188
Dravet Syndrome-Genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children Proceeding/Conference:International Meeting for Autism Research	Wong, VCN Kwong, AKY Fung, CW	2012	161
Effect of olive oil phenol hydroxytyrosol (HT) in patient cell model with mitochondrial complex deficiency Proceeding/Conference:Joint Annual Scientific Meeting 2020 (Virtual Meeting) of The Hong Kong Paediatric Society (HKPS), Hong Kong College of Paediatricians (HKCPaed), Hong Kong Paediatric Nurses Association (HKPNA) and Hong Kong College of Paediatric Nursing (HKCPN)	Kwong, AKY Fung, CW	2020	34
Exome sequencing for paediatric-onset diseases: impact of the extensive involvement of medical geneticists in the diagnostic odyssey Journal:npj Genomic Medicine	Mak, CCY Leung, KC Mok, TKG Yeung, KS Yang, W Fung, CW Chan, HSS Lee, SL Lee, NC Pfundt, R Lau, YL Chung, BHY	2018	95
Exome sequencing identifies molecular diagnosis in children with drug-resistant epilepsy Journal:Epilepsia Open	Tsang, HY Leung, KC Ho, CCA Yeung, KS Mak, CCY Pei, LCS Yu, HC Kan, SYA Chan, YK Kwong, KL Lee, SL Yung, AWY Fung, CW Chung, BHY	2019	111

Showing results 13 to 32 of 97 < previous next >