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	Title	Author(s)	Issue Date
	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
	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
	Novel POLG mutation in a patient with sensory ataxia, neuropathy, ophthalmoparesis and stroke Journal:Clinica Chimica Acta	Lam, CW Law, CY Siu, CWK Fung, CW Yau, MM Huen, KF Lee, HHC Mak, CM	2015
	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
	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
	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

Showing results 2 to 7 of 7 < previous