Browsing by Author Chan, YW

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TitleAuthor(s)Issue Date
 
Application of text analytics in examining students’ qualitative feedback in relation to teaching and learning.
Proceeding/Conference:International Conference on Learning and Teaching (ICLT) 2020
Ko, WTChan, YWZhao, Y
2020
 
Beta-thromboglobulin in cerebral infarction
Journal:Journal of Neurology Neurosurgery and Psychiatry
Woo, EHuang, CYChan, VChan, YWYu, YLChan, TK
1988
 
Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese
Journal:Molecular Genetics and Metabolism
Mak, CMLam, CWSiu, TSChan, KYSiu, WKYeung, WLHui, JWong, VCNLow, LCKKo, CHFung, CWChen, SPYuen, YPLee, HCYau, EChan, BTong, SFTam, SChan, YW
2010
 
Circulating fluorocytes at the first attack of acute intermittent porphyria: A missing link in the pathogenesis
Journal:Clinica Chimica Acta
Lam, CWLau, KCMak, CMTsang, MWChan, YW
2011
 
Cloning and Identification of The Glycoprotein C Gene and Thymidine Kinase Gene of Infectious Laryngotracheitis Virus (ILTV) Beijing E2 Strain
Proceeding/Conference:International Symposium of Society of Chinese Bioscientists in America
Wu, HChan, YWLeung, FCC
1999
 
A dangerous gluteal injection
Journal:Journal of the Hong Kong Medical Association
Woo, EChan, YWKwong, YL
1986
 
Diagnosis of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes in a Chinese family by PCR/restriction enzyme analysis
Journal:Journal of Clinical Pathology - Clinical Molecular Pathology
Lam, CWJain, KChan, KYSilva, DKChan, YWWong, LJC
1995
 
DNA analysis of Huntington's disease in Southern Chinese
Journal:Journal of Medical Genetics
Chan, VYu, YLChan, TPTYip, BChang, CMWong, MTHChan, YWChan, TK
1995
 
DNA-based diagnosis of isolated sulfite oxidase deficiency by denaturing high-performance liquid chromatography
Journal:Molecular Genetics and Metabolism
Lam, CWLi, CKLai, CKTong, SFChan, KYNg, GSFYuen, YPCheng, AWFChan, YW
2002
 
DNA-based diagnosis of methylmalonic aciduria and homocystinuria, cblC type in a Chinese patient presenting with mild developmental delay
Journal:Clinica Chimica Acta
Yuen, YPLam, CWChan, KYLai, CKTong, SFChan, YW
2007
 
Electrophysiological Mechanisms of Brugada Syndrome: Insights from Pre-clinical and Clinical Studies
Journal:Frontiers in Physiology
Tse, GLiu, TLi, KHLaxton, VChan, YWKeung, WWYLi, RAYan, BP
2016
 
Electrophysiological mechanisms of long and short QT syndromes
Journal:IJC Heart & Vasculature
Tse, GChan, YWKeung, WWYYan, BP
2017
 
Encephalopathy and neuropathy following ingestion of a Chinese herbal broth containing podophyllin
Journal:Journal of the Neurological Sciences
Ng, THKChan, YWYu, YLChang, CMHo, HCLeung, SYBhut, PPH
1991
 
Epidemiological study of multiple sclerosis in Hong Kong Chinese: questionnaire survey
Lau, KKWong, LKSLi, LSWChan, YWLi, HLWong, V
2002
 
Ethnic-specific splicing mutation of the carnitine-acylcarnitine translocase gene in a Chinese neonate presenting with sudden unexpected death
Journal:Chinese Medical Journal
Lam, CWLai, CKChow, CBTong, SFYuen, YPMak, YFChan, YW
2003
 
Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience
Journal:Hong Kong Medical Journal
Mak, CMChen, SPLMok, NSSiu, WKLee, HHCChing, DCKTsui, PTFong, NCYuen, YPPoon, DWTLaw, CYChong, YKChan, YWYung, TCFan, KYLam, CW
2018
 
Germline epimutation of MLH1 in early-onset colorectal cancer
Proceeding/Conference:Cancer Research
Chan, TLTsui, WYChan, YWChan, ASYLee, TYHYuen, STLeung, SY
2008
 
Germline methylation of the MSH2 promoter as a cause of Hereditary Non-Polyposis Colorectal Cancer
Proceeding/Conference:Cancer Research
Chan, TLYuen, STHo, JWCChan, YWChan, ASYChan, EMSLeung, SY
2005
 
Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer
Journal:Nature Genetics
Chan, TLYuen, STKong, CKChan, YWChan, ASYNg, WFTsui, WYLo, MWSTam, WYLi, VSWLeung, SY
2006
 
Heritable germline epimutation of MSH2 in a hereditary nonpolyposis colorectal cancer family
Proceeding/Conference:Biennial Scientific Meeting of the International Society for Gastrointestinal Hereditary Tumours, InSiGHT 2007
Chan, TLYuen, STKong, CKChan, YWChan, ASYLeung, SY
2007
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