HKU Scholars Hub: Browsing DSpace

Browsing by Author Fung, CW

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 中

or enter first few letters:

Showing results 75 to 94 of 97 < previous next >

Title	Author(s)	Issue Date	Views
SCN2A mutation in a Chinese boy with infantile spasm - response to Modified Atkins Diet Journal:Brain and Development	Wong, VCN Fung, CW Kwong, KY	2015	75
Spectrum of anticonvulsant hypersensitivity syndrome: Controversy of treatment Journal:Journal of Child Neurology	Lee, WC Leung, JLS Fung, CW Chung, BHY Wong, V	2004	158
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong Proceeding/Conference:International Symposium on Epilepsy in Neurometabolic Diseases, ISENMD 2010 Proceedings	Fung, CW Poon, G Kwok, A Cheung, PT Low, L Mak, C Tam, S Siu, S Wong, V	2010	106
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong Proceeding/Conference:Developmental Medicine and Child Neurology	Fung, CW Smeitenk, J Rodenburg, R Siu, S Ma, O Poon, G Tam, S Wong, V	2012
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong Proceeding/Conference:Hospital Authority Convention, HAC 2011	Wong, VCN Fung, CW	2011	79
Stiff child syndrome with mutation of DYT1 gene Journal:Neurology	Wong, VCN Lam, CW Fung, CW	2005
A study of cerebrospinal fluid neurotransmitters assay in children with undiagnosed neurological diseases in Hong Kong Proceeding/Conference:International Symposium on Epilepsy in Neurometabolic Diseases, ISENMD 2010 Proceedings	Fung, CW Poon, G Kwok, A Cheung, PT Low, L Blau, N Siu, S Mak, C Tam, S Wong, V	2010	155
A study of cerebrospinal fluid neurotransmitters assay in children with undiagnosed neurological diseases in Hong Kong Proceeding/Conference:Hong Kong Medical Journal	Fung, CW Siu, S Poon, G Kwok, A Cheung, PT Low, L Mak, C Tam, S Wong, VCN	2009	174
The epileptology of GNB5 encephalopathy Journal:Epilepsia	Poke, G King, C Muir, A de Valles-Ibariez, G Germano, M Moura de Souza, CF Fung, J Chung, B Fung, CW Mignot, C Ilea, A Keren, B Vermersch, AI Davis, S Stanley, T Moharir, M Kannu, P Shao, Z Malerba, N Merla, G Mefford, HC Scheffer, IE Sadleir, LG	2019	22
The KLHL40 c.1516A>C is a Chinese‐specific founder mutation causing nemaline myopathy 8: Report of six patients with pre‐ and postnatal phenotypes Journal:Molecular Genetics & Genomic Medicine	Yeung, KS Yu, FNY Fung, CW Wong, S Lee, HCH Fung, STH Fung, GPG Leung, KY Chung, WH Lee, YT Ng, VKS YU, HC Fung, JLF TSANG, MHY Chan, KYK Chan, SHS Kan, ASY Chung, BHY	2020	49
The KLHL40C.1516A>C is a Chinese-specific founder mutation in causing nemaline myopathy 8 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	Yeung, KS Yu, YN Fung, CW Wong, S Lee, HCH Fung, STH Fung, GPG Yu, MHC Fung, JLF Tsang, MHY Chan, YK Chan, HSS Kan, SYA Chung, BHY	2019
Topiramate-valproate-induced hyperammonemic encephalopathy syndrome: Case report Journal:Journal of Child Neurology	Cheung, E Wong, V Fung, CW	2005
Two novel mutations of SMPD1 gene from a Chinese family with Niemann Pick Disease type A (NPD-A) Proceeding/Conference:HKPS-HKPNA 2006 Joint Annual Scientific Meeting	Chung, BHY Fung, CW Li, YH Wong, KY Chan, GCF Wong, VCN	2006	100
Two novel mutations of SMPD1 gene from a Chinese family with Niemann Pick Disease Type A (NPD-A) Proceeding/Conference:50th Anniversary Symposium on Paediatric Neurology & Neuro-Rehabilitation	Chung, BHY Fung, CW Li, YH Wong, KY Chan, GCF Wong, VCN	2005	79
Two novel mutations of SMPD1 gene from a Chinese family with niemann pick disease type A (NPD-A) Proceeding/Conference:Hong Kong Medical Genetics Conference	Chung, BHY Fung, CW Li, S Wong, KY Chan, GCF Wong, VCN	2005	97
Unusual presentation of severe neonatal form of nemaline rod myopathy - ophthalmoplegia and ptosis Proceeding/Conference:Brain & Development	Lee, S Wong, VCN Fung, CW Ip, P Leung, SY	2002	105
Urine organic acid as the first clue towards aromatic L-amino acid decarboxylase (AADC) deficiency in a high prevalence area Journal:Clinica Chimica Acta	Ling, TK Wong, KC Chan, CY Lau, NKC Law, CY Lee, HCH Lai, CK Chong, YK Yau, KCE Cheung, KM Ko, CH Fung, CW Lee, LK Wong, SSN Mak, CM Chan, AYW Tam, S Lam, CW	2021	23
Use of chromosomal microarray in Hong Kong patients with autism spectrum disorder - implication of a copy number variation involving DPP10 Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2016	Chung, BHY Mak, SL Chiu, TA Leung, KC Mak, CCY Chu, WY Mok, TKG Chan, YK Kan, SYA Tang, MHY Lau, ETK Fung, CW Lee, SL	2016	45
Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving DPP10 Journal:Molecular Autism	Mak, ASL Chiu, TA Leung, KC Mak, CCY Chu, WY Mok, TKG Tang, WF Chan, YK Tang, MHY Lau, ETK So, KW Tao, QV Fung, CW Wong, CNV Uddin, M Lee, SL Marshall, CR Scherer, SW Kan, ASY Chung, BHY	2017	181
Use of clinical chromosomal microarray in Hong Kong Chinese patients with autism spectrum disorder - implication of a copy number variation involving DPP10 Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Chu, YWY Leung, KC Mak, ASL Chiu, TA Mak, CCY Mok, TKG Tang, WF Chan, YK Tang, MHY Lau, ETK So, KW Tao, QV Fung, CW Wong, VCN Lee, SL Marshall, C Scherer, S Kan, SYA Chung, BHY	2016	84

Showing results 75 to 94 of 97 < previous next >