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	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	318
	Deoxythymidylate kinase, DTYMK, is a novel gene for mitochondrial DNA depletion syndrome Journal:Clinica Chimica Acta	Lam, CW YEUNG, WL Ling, TK Wong, KC LAW, CY	2019	40
	Early-onset primary torsional dystonia in a 4-generation Chinese family with a mutation in the DYT1 gene Journal:Chinese Medical Journal	Yeung, WL Lam, CW Cheng, WT Sin, NC Wong, WK Wong, CN Tse, KM Fok, TF	2005	108
	Evidence for cerebral embolic prevention in transcatheter aortic valve implantation and thoracic endovascular aortic repair Journal:Annals of Vascular Surgery	Lam, HT Kwong, JM Lam, PL Yeung, WL Chan, YC	2019	29
	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	235
	Galactorrhea-A strong clinical clue towards the diagnosis of neurotransmitter disease Journal:Brain and Development	Yeung, WL Lam, CW Hui, J Tong, SF Wu, SP	2006	210
	Global developmental delay and intellectual disability associated with a de novo TOP2B mutation Journal:Clinica Chimica Acta	Lam, CW Yeung, WL Law, CY	2017	48
	How do laymen make sense of the law: a case study of unrepresented litigants in Hong Kong Proceeding/Conference:Hong Kong as Method (香港作為方法) International Conference	Yeung, WL	2014	24
	Intra-familial variation in clinical manifestations and response to ephedrine in siblings with congenital myasthenic syndrome caused by novel COLQ mutations Journal:Developmental Medicine and Child Neurology	Yeung, WL Lam, CW Ng, PC	2010	139
	Lay participation of common law: understanding the semiotic specificity of law through the eyes of unrepresented litigants Proceeding/Conference:Law and Society in the 21st Century Conference	Yeung, WL	2015	30
	Prevalence and Characteristics of Chinese Patients With Duchenne and Becker Muscular Dystrophy-A Territory Wide Collaborative Study in Hong Kong Journal:Child Neurology Open	Chan, SHS Lo, IFM Cherek, S Cheng, WW Fung, EL Yeung, WL Ngan, M Lee, WC Kwong, L Wong, SN Ma, CK Tai, SM Ng, SF Wu, SP Wong, VCN	2015	133
	Progesterone is more effective than dexamethasone in prolonging overall survival and preserving neurologic function in experimental animals with orthotopic glioblastoma allografts Journal:World Neurosurgery	Cheng, Y Yeung, WL Zhang, P Li, N Kiang, MY Leung, GKK	2019	54
	Removing linguistic barriers to justice: a study of official reference texts for unrepresented litigants Proceeding/Conference:International Conference on Law, Language and Discourse, LLD-2	Yeung, WL Leung, JHC	2012	46
	Removing linguistic barriers to justice: a study of official reference texts for unrepresented litigants in Hong Kong Journal:International Journal for the Semiotics of Law	Yeung, WL Leung, JHC	2015	98
	Severe congenital myasthenia gravis of the presynaptic type with choline acetyltransferase mutation in a Chinese infant with respiratory failure Journal:Neonatology	Yeung, WL Lam, CW Fung, LWE Hon, KLE Ng, PC	2009	175
	Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome. Journal:Journal of medical genetics	Lam, CW Yeung, WL Ko, CH Poon, PM Tong, SF Chan, KY Lo, IF Chan, LY Hui, J Wong, V Pang, CP Lo, YM Fok, TF	2000	175
	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	55
	Understanding the semiotic specificity of law through the eyes of unrepresented litigants Journal:Semiotica	Yeung, WL Leung, JHC	2017	70

Showing results 3 to 20 of 20 < previous