Browsing by Author Chan, YW

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 中
Showing results 26 to 45 of 73 < previous   next >
TitleAuthor(s)Issue DateViews
 
Management of tetanus: A review of 18 cases
Journal:Journal of the Royal Society of Medicine
Sun, KOChan, YWCheung, RTFSo, PCYu, YLLi, PCK
1994
150
 
Maternally inherited leigh syndrome: An unusual cause of infantile apnea
Journal:Sleep and Breathing
Chau, CSKKwok, KLNg, DKLam, CWTong, SFChan, YWSiu, WKYuen, YP
2010
177
 
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
125
 
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
 
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
203
 
Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) triggered by valproate therapy
Journal:European Journal of Pediatrics
Lam, CWLau, CHWilliams, JCChan, YWWong, LJC
1997
105
 
Molecular characterization of the 2011 Hong Kong scarlet fever outbreak
Journal:Journal of Infectious Diseases
Tse, HBao, JYJDavies, MRMaamary, PTsoi, HWTong, AHYHo, TCCLin, CHGillen, CMBarnett, TCChen, JHKLee, MYam, WCWong, CKOng, CLYChan, YWWu, CWNg, TLim, WWLTsang, THFTse, CWSDougan, GWalker, MJLok, SYuen, KY
2012
220
 
Molecular Identification and Characterization of The Hog Cholera Virus From Hong Kong and South China
Proceeding/Conference:International Symposium of Society of Chinese Bioscientists in America
Wong, KMWu, HChan, YWLeung, FCC
1999
98
 
Molecular Identification of Hog Cholera Viruses from Southern China
Journal:Journal of Animal and Veterinary Advances
Wu, HZChan, YWWong, KMLeung, FCC
2005
99
 
Motor neuron disease in Hong Kong Chinese: Epidemiology and clinical picture
Journal:Neuroepidemiology
Fong, KYYu, YLChan, YWKay, RChan, JYang, ZKwan, MCLeung, KPLi, PCKLam, THCheung, RTF
1996
174
 
Motor Neurone Disease (MND) in Hong Kong Chinese: Neuroepidemiology and Clinical Features
Proceeding/Conference:1st Asian-Oceanian Symposium in neuroepidemiology & 2nd Wu Ho-Su Memorial Lecture
Fong, KYYu, YLChan, YWLeung, KPLi, PCKLam, THYang, ZKwan, MCKay, RChan, JCheung, RTF
1994
 
Mouse models of atherosclerosis: a historical perspective and recent advances
Journal:Lipids in Health and Disease
Lee, YTLin, HYChan, YWLi, KHTo, OTYan, BPLiu, TLi, GPWong, WTKeung, WWYTse, G
2017
113
 
MSH2 c.1452-1455delAATG Is a Founder Mutation and an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Southern Chinese Population
Journal:American Journal of Human Genetics
Chan, TLChan, YWHo, JWCChan, CChan, ASYChan, ELam, PWYTse, CWLee, KCLau, CWGwi, ELeung, SYYuen, ST
2004
134
 
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity
Journal:Journal of Human Genetics
Mak, CMLam, CWTam, SLai, CLChan, LYFan, STLau, YLLai, JYYuen, PHui, JFu, CCWong, KSMak, WLTze, KTong, SFLau, ALeung, NHui, ACheung, KMKo, CHChan, YKMa, OChau, TNChiu, AChan, YW
2008
 
Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: Identification of 17 novel mutations and its genetic heterogeneity (Journal of Human Genetics (2008) 53 (55-63) DOI: 10.1007/s10038-007-0218-2)
Journal:Journal of Human Genetics
Mak, CMLam, CWTam, SLai, CLChan, LYFan, STLau, YLLai, STYuen, PHui, JFu, CCWong, KSMak, WLTze, KTong, SFLau, ALeung, NHui, ACheung, KMKo, CHChan, YKMa, OChau, TNChiu, AChan, YW
2008
 
Non-invasive screening of HLA-DPA1 and HLA-DPB1 alleles for persistent hepatitis B virus infection: Susceptibility for vertical transmission and toward a personalized approach for vaccination and treatment
Journal:Clinica Chimica Acta
Lau, KCLam, CWLaw, CYLai, STTsang, TYSiu, CWKTo, WKLeung, KFMak, CMPoon, WTChan, PKSChan, YW
2011
150
 
Novel donor splice site mutation of ABCG5 gene in sitosterolemia
Journal:Molecular Genetics and Metabolism
Lam, CWCheng, AWFTong, SFChan, YW
2002
180
 
A novel missense mutation (P191L) in the glucose-6-phosphate translocase gene identified in a Chinese family with glycogen storage disease 1b.
Journal:Human mutation
Lam, CWChan, KYTong, SFChan, BYChan, YTChan, YW
2000
 
Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b
Journal:Molecular Genetics and Metabolism
Yuen, YPCheng, WFTong, SFChan, YTChan, YWLam, CW
2002
178
 
Novel missense mutation (Y279S) in the GLRA1 gene causing hyperekplexia [2]
Journal:Clinica Chimica Acta
Poon, WTAu, KMChan, YWChan, KYChow, CBTong, SFLam, CW
2006
178
Showing results 26 to 45 of 73 < previous   next >