Browsing by Author Chan, YW

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TitleAuthor(s)Issue DateViews
 
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
81
 
Electrophysiological mechanisms of long and short QT syndromes
Journal:IJC Heart & Vasculature
Tse, GChan, YWKeung, WWYYan, BP
2017
88
 
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
194
 
Epidemiological study of multiple sclerosis in Hong Kong Chinese: questionnaire survey
Lau, KKWong, LKSLi, LSWChan, YWLi, HLWong, V
2002
195
 
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
125
 
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
87
 
Germline epimutation of MLH1 in early-onset colorectal cancer
Proceeding/Conference:Cancer Research
Chan, TLTsui, WYChan, YWChan, ASYLee, TYHYuen, STLeung, SY
2008
142
 
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
96
 
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
138
 
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
95
 
Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria
Journal:Kidney International
Yuen, YPLam, CWLai, CKTong, SFLi, PSTam, SKwan, EYWChan, SYTsang, WKChan, KYMak, WLCheng, CWChan, YW
2006
218
 
High-performance thin-layer chromatography of free porphyrins for diagnosis of porphyria
Journal:Clinical Chemistry
Lai, CKLam, CWChan, YW
1994
132
 
Huntington's disease in Hong Kong Chinese: epidemiology and clinical picture.
Journal:Clinical and experimental neurology
Chang, CMYu, YLFong, KYWong, MTHChan, YWNg, THLeung, CMChan, V
1994
288
 
Immunohistochemical staining on tissue microarray of colorectal cancers constitutes a convenient means to rapidly screen for MMR deficiency
Proceeding/Conference:Biennial Scientific Meeting of the International Society for Gastrointestinal Hereditary Tumours, InSiGHT 2007
Chan, TLGuo, DYuen, STChan, YWChan, ASYLeung, SY
2007
116
 
Juvenile-onset glycogen storage disease type II with novel mutations in acid α-glucosidase gene
Journal:Neurology
Lam, CWYuen, YPChan, KYTong, SFLai, CKChow, TCLee, KCChan, YWMartiniuk, F
2003
168
 
Management of tetanus: A review of 18 cases
Journal:Journal of the Royal Society of Medicine
Sun, KOChan, YWCheung, RTFSo, PCYu, YLLi, PCK
1994
137
 
Maternally inherited leigh syndrome: An unusual cause of infantile apnea
Journal:Sleep and Breathing
Chau, CSKKwok, KLNg, DKLam, CWTong, SFChan, YWSiu, WKYuen, YP
2010
166
 
Measuring Longitudinal Gains in Student Learning: A Comparison of Rasch Scoring and Summative Scoring Approaches
Journal:Research in Higher Education
Zhao, YHUEN, MYJChan, YW
2017
107
 
Microsatellite instability and novel mismatch repair gene mutations in northern Chinese population with hereditary non-polyposis colorectal cancer.
Journal:Chinese journal of digestive diseases
Sheng, JQChan, TLChan, YWHuang, JSChen, JGZhang, MZGuo, XLMu, HChan, ASLi, SRYuen, STLeung, SY
2006
151
 
Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome
Journal:Clinica Chimica Acta
Lam, CWYuen, YPCheng, WFChan, YWTong, SF
2006
191
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