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Showing results 1 to 11 of 11

	Title	Author(s)	Issue Date	Views
	Congenital Myopathies are a Group of Phenotypically and Genetically Heterogeneous Diseases Proceeding/Conference:Hong Kong Medical Journal	Chan, HSS Ho, RSL Chan, AOK Ip, JK Wong, S Ng, G Lee, H Cheng, SY Liu, KT Lee, CN Fung, ST Cherk, SW Chan, TS Lam, W Shek, WT Wong, CNV	2016	18
	Congenital myopathies: characteristic and subtypes in Hong Kong Proceeding/Conference:Neuromuscular Disorders	Chan, HSS Ho, RSL Chan, AOK Ip, JJK Wong, S Ng, GSF Lee, HCH Cheng, Y Liu, KT Lee, CN Fung, STH Cherk, SWW Chan, TSK Lam, WMW Shek, WH Wong, VCN	2015	58
	Exome sequencing in paediatric patients with movement disorders [accepted - OJRD-D-20-00713R2] Journal:Orphanet Journal of Rare Diseases	Kwong, AKY TSANG, MHY Fung, JLF Mak, CCY Chan, KLS Rodenburg, RJT Lek, M Huang, S Pajusalu, S Yau, MM Tsoi, C Fung, S Liu, KT Ma, CK Wong, S Yau, EKC Tai, SM Fung, ELW Wu, NSP Tsung, LY Smeitink, J Chung, BHY Fung, CW	2021	44
	Functional Independence Measure (WeeFIM) for Chinese children: Hong Kong Cohort. Journal:Pediatrics	Wong, V Wong, S Chan, K Wong, W	2002	125
	Klein Levin syndrome is a steroid-responsive, non-N-methyl-D-aspartate receptor-mediated encephalitis Proceeding/Conference:Hong Kong Medical Journal	Wong, S Cheung, P Wong, VCN Ma, L Chan, B	2012	25
	Klein Levin Syndrome is a steroid-responsive, non-N-methyl-D-aspartate receptor-mediated encephalitis Proceeding/Conference:Developmental Medicine and Child Neurology	Wong, S Cheung, P Wong, V Chan, B	2012	206
	Myofibrillar myopathies: a clinicopathological study of 13 cases Proceeding/Conference:Asian and Oceanian Myology Center Annual Scentific Meeting, AOMC 2016	Wong, S Lee, H Lee, CN Cheng, Y Cheung, YF Fu, M Sheung, B Ho, R Ho, LC Chang, SK Fung, S Yau, E Kan, A Chan, A Chan, HSS	2016	24
	Territory wide study of patients with dystrophinopathy in Hong Kong Proceeding/Conference:Neuromuscular Disorders	Chan, SHS Lo, IFM Cherk, S Cheng, WWS Fung, E Yeung, WL Lee, WC Wong, S Ma, CKL Tai, SM Yau, MM Ng, G Wu, SP Wong, VCN	2013	45
	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
	Use of chopsticks in Chinese children Journal:Child: Care, Health and Development	Wong, S Chan, K Wong, V Wong, W	2002

Showing results 1 to 11 of 11