Results 1 to 9 of 9
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TypeTitleAuthor(s)YearViews
Removing linguistic barriers to justice: a study of official reference texts for self-represented litigants in Hong KongYeung, WL; Leung, JHC201357
 
Removing linguistic barriers to justice: a study of official reference texts for unrepresented litigantsYeung, WL; Leung, JHC201242
 
Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiencyYeung, WL; Wong, VCN; Chan, KY; Hui, J; Fung, CW; Yau, E; Ko, CH; Lam, CW; Mak, CM; Siu, S; Low, L2011218
 
Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong ChineseMak, 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, YW2010239
 
Intra-familial variation in clinical manifestations and response to ephedrine in siblings with congenital myasthenic syndrome caused by novel COLQ mutationsYeung, WL; Lam, CW; Ng, PC2010147
 
Severe congenital myasthenia gravis of the presynaptic type with choline acetyltransferase mutation in a Chinese infant with respiratory failureYeung, WL; Lam, CW; Fung, LWE; Hon, KLE; Ng, PC2009133
 
Galactorrhea-A strong clinical clue towards the diagnosis of neurotransmitter diseaseYeung, WL; Lam, CW; Hui, J; Tong, SF; Wu, SP200680
 
Early-onset primary torsional dystonia in a 4-generation Chinese family with a mutation in the DYT1 geneYeung, WL; Lam, CW; Cheng, WT; Sin, NC; Wong, WK; Wong, CN; Tse, KM; Fok, TF200580
 
Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.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, TF2000335
 
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