Browsing by Author Yuen, YP

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TitleAuthor(s)Issue DateViews
 
Chemical pathology case conference - Assessment of iron status in general practice
Journal:Hong Kong Practitioner
Mak, CMChiu, RWKLam, CWChan, AYWMak, TWLShek, AChan, MHMTai, MHLYuen, YPPoon, WTTam, S
2006
229
 
Chemical pathology case conference - Common endocrine tests
Journal:Hong Kong Practitioner
Tai, MHLMak, CMYuen, YPLam, CWChiu, RWKChan, MHMChan, AYWShek, ACCMak, TWLPoon, WTTam, S
2007
120
 
Chemical pathology case conference - Laboratory tests for diabetes mellitus
Journal:Hong Kong Practitioner
Yuen, YPMak, CMChan, AOKChan, MHMChiu, RWKLam, CWMak, TWLPoon, WTShek, ACCTai, MHLTam, SChan, AYW
2007
153
 
Chemical pathology case conference - Renal function tests
Journal:Hong Kong Practitioner
Yuen, YPTam, SChan, AKCMak, TWLLam, CWShek, ACCChiu, RWKChan, MHMTai, MHLChan, AYW
2006
145
 
Chemical pathology case conference - Serum tumour markers
Journal:Hong Kong Practitioner
Poon, WTYuen, YPMak, CMChan, AOKChan, MHMChiu, RWKLam, CWMak, TWLShek, CCTai, MHLTam, SChan, AYW
2010
147
 
Diagnosis of dihydropyrimidine dehydrogenase deficiency in a neonate with thymine-uraciluria
Journal:Hong Kong Medical Journal
Au, KMLai, CKYuen, YPShek, CCLam, CWChan, AYW
2003
117
 
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
197
 
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
185
 
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
134
 
Fatal viral infection-associated encephalopathy in two Chinese boys: A genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants
Journal:Journal of Human Genetics
Mak, CMLam, CWFong, NCSiu, WKLee, HCHSiu, TSLai, CKLaw, CYTong, SFPoon, WTLam, DSYNg, HLYuen, YPTam, SQue, TLKwong, NSChan, AYW
2011
202
 
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
61
 
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
226
 
In search of the diagnosis, and the patient: transient galactosemia demystified after 14 years
Journal:Genetic Counseling
Lee, HHCLam, CWYuen, YPLai, CKChan, KYChan, AYW
2012
62
 
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
167
 
Maternally inherited leigh syndrome: An unusual cause of infantile apnea
Journal:Sleep and Breathing
Chau, CSKKwok, KLNg, DKLam, CWTong, SFChan, YWSiu, WKYuen, YP
2010
159
 
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
183
 
Molecular basis of von Hippel-Lindau syndrome in Chinese patients
Journal:Chinese Medical Journal
Siu, WKMa, RCWLam, CWMak, CMYuen, YPLo, FMIChan, KWLam, SFLing, SCTong, SFSo, WYChow, CCTang, MHYTam, WHChan, AYW
2011
302
 
Non-invasive urinary screening for aromatic l-amino acid decarboxylase deficiency in high-prevalence areas: A pilot study
Journal:Clinica Chimica Acta
Lee, HCHLai, CKYau, KCESiu, TSMak, CMYuen, YPChan, KYTam, SLam, CWChan, AYW
2012
196
 
A novel duplication at the putative DNA polymerase alpha arrest site and a founder mutation in Chinese in the IVD gene underlie isovaleric acidaemia
Journal:Hong Kong Medical Journal
Lee, HHCLee, RSYLai, CKYuen, YPSiu, TSChan, AYWLam, CW
2010
151
 
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
172
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