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	Title	Author(s)	Issue Date
	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
	Mitochondrial diseases in Hong Kong: prevalence, clinical characteristics and genetic landscape Journal:Orphanet Journal of Rare Diseases	Wong, TS Belaramani, KM Chan, CK Chan, WK Chan, WLL Chang, SK Cheung, SN Cheung, KY Cheung, YF Chong, SCJ Chow, CKJ Chung, HYB Fan, SYF Fok, WMJ Fong, KW Fung, THS Hui, KF Hui, TH Hui, JN Ko, CH Kwan, MC Kwok, MKA Kwok, SSJ Lai, MS Lam, YO Lam, CW Lau, MC Law, CYE Lee, WC Lee, HCH Lee, CN Leung, KH Leung, KY Li, SH Ling, TKJ Liu, KTT Lo, FM Lui, HT Luk, CO Luk, HM Ma, CK Ma, KR Ma, KH Mew, YN Mo, AL Ng, SF Poon, WKG Rodenburg, R Sheng, B Smeitink, J Szeto, CLC Tai, SM Tse, CTA Tsung, LL Wong, HMJ Wong, WYW Wong, KK Wong, SNS Wong, CNV Wong, WSS Wong, CKF Wu, SP Wu, HFJ Yau, MM Yau, KCE Yeung, WL Yeung, HMJ Yip, KKE Young, PHT Yuan, G Yuen, YPL Yuen, CL Fung, CW	2-Mar-2023
	Lathosterolosis: A Disorder Of Cholesterol Biosynthesis Resembling Smith-lemli-opitz Syndrome Journal:Journal Of Inherited Metabolic Disease	Ho, CCA Fung, CW Siu, TS Ma, OCK Lam, CW Tam, S Wong, VCN	2014
	Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiency Journal:Journal of Child Neurology	Yeung, WL Wong, VCN Chan, KY Hui, J Fung, CW Yau, E Ko, CH Lam, CW Mak, CM Siu, S Low, L	2011
	Dystrophin staining in Duchenne and Becker muscular dystrophy Proceeding/Conference:Annual Meeting of the Hong Kong Division of the International Academy of Pathology	Leung, SY Lau, YL Wong, VCN Ho, FCS Lau, P Srivastava, G	1993
	Diagnosis of Subacute Sclerosing Panencephalitis (SSPE) - beyond EEG and measles serology Proceeding/Conference:ICNA-AOCNA 2002 Joint Congress	Chung, BHY Ip, P Wong, VCN Lo, J Nicholls, JM Khong, PL	2002
	A boy with subacute sclerosing panencephalitis (SSPE) - diagnostic challenge Proceeding/Conference:Neuropathology 2002	Wong, VCN Chung, BHY Ip, P Nicholls, JM Lo, J	2002
	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
	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
	Acute fulminant SSPE with absent measels and PCR studies in cerebrospinal fluid Proceeding/Conference:50th Anniversary Symposium on Paediatric Neurology & Neuro-Rehabilitation	Chung, BHY Ip, P Wong, VCN Lo, J Nicholls, JM Khong, PL	2005

Showing results 1 to 10 of 10