Results 1 to 12 of 12
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TypeTitleAuthor(s)YearViews
Characteristic of patients with Duchenne Muscular Dystrophy and Becker Muscular Dystrophy in Hong Kong
Journal:
Journal of Paediatric Neurology
Chan, SHS; Lo, IFM; Cherk, S; Cheng, WW; Fung, ELW; Yeung, WL; Ngan, M; Lee, WC; Kwong, L; Wong, SN; Ma, CK; Tai, SM; Ng, SF; Wu, SP; Wong, VCN201414
 
Characteristic of patients with Duchenne Muscular Dystrophy and Becker Muscular Dystrophy in Hong Kong
Journal:
Paediatric Neurology
Chan, SHS; Lo, IFM; Cherek, S; Cheng, WW; Fung, EI; Yeung, WL; Ngan, M; Lee, WC; Kwong, L; Wong, SN; Ma, CK; Tai, SM; Ng, SF; Wu, SP; Wong, VCN201437
 
Removing linguistic barriers to justice: a study of official reference texts for self-represented litigants in Hong Kong
Journal:
Meta: Translator’s Journal
Yeung, WL; Leung, JHC201386
 
Territory wide study of patients with dystrophinopathy in Hong Kong
Proceedings/Conference:
Neuromuscular Disorders
Publisher:
Elsevier Ltd. The Journal's web site is located at http://www.elsevier.com/locate/nmd
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, VCN201345
 
Removing linguistic barriers to justice: a study of official reference texts for unrepresented litigants
Proceedings/Conference:
2nd International Conference on Law, Language and Discourse, LLD2
Yeung, WL; Leung, JHC201267
 
Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiency
Journal:
Journal of Child Neurology
Publisher:
Sage Publications, Inc.. The Journal's web site is located at http://jcn.sagepub.com
Yeung, WL; Wong, VCN; Chan, KY; Hui, J; Fung, CW; Yau, E; Ko, CH; Lam, CW; Mak, CM; Siu, S; Low, L2011297
 
Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese
Journal:
Molecular Genetics and Metabolism
Publisher:
Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/ymgme
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, YW2010307
 
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
Publisher:
Mac Keith Press. The Journal's web site is located at http://www.mackeith.co.uk/journal.html
Yeung, WL; Lam, CW; Ng, PC2010189
 
Severe congenital myasthenia gravis of the presynaptic type with choline acetyltransferase mutation in a Chinese infant with respiratory failure
Journal:
Neonatology
Publisher:
S Karger AG. The Journal's web site is located at http://www.karger.com/BON
Yeung, WL; Lam, CW; Fung, LWE; Hon, KLE; Ng, PC2009206
 
Galactorrhea-A strong clinical clue towards the diagnosis of neurotransmitter disease
Journal:
Brain and Development
Publisher:
Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/braindev
Yeung, WL; Lam, CW; Hui, J; Tong, SF; Wu, SP2006121
 
Early-onset primary torsional dystonia in a 4-generation Chinese family with a mutation in the DYT1 gene
Journal:
Chinese Medical Journal
Publisher:
Zhonghua Yixuehui. The Journal's web site is located at http://www.cmj.org/
Yeung, WL; Lam, CW; Cheng, WT; Sin, NC; Wong, WK; Wong, CN; Tse, KM; Fok, TF2005131
 
Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.
Journal:
Journal of medical genetics
Publisher:
B M J Publishing Group. The Journal's web site is located at http://jmg.bmjjournals.com/
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, TF2000377
 
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