Results 1 to 8 of 8
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Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome: a treatable genetic liver disease warranting urgent diagnosis
Hong Kong Med J
Lee, HHC; Poon, KH; Lai, CK; Au, KM; Siu, TS; Lai, JP; Mak, CM; Yuen, YP; Lam, CW; Chan, AYW20145
2,4-Dinitrophenol: A threat to Chinese body-conscious groups
J Chin Med Assoc
Lee, HHC; Law, CY; Chen, ML; Lam, YH; Chan, AY; Mak, TW20144
Cost-benefit analysis of Hyperphenylalaninemia Due to 6-Pyruvoyl-Tetrahydropterin Synthase (PTPS) Deficiency: For Consideration of Expanded Newborn Screening in Hong Kong
J Med Screen
Lee, HHC; Mak, CM; Poon, WKG; Wong, KY; Lam, CW20148
Inborn errors of metabolism and expanded newborn screening: review and update
Crit Rev Clin Lab Sci
Mak, CM; Lee, HHC; Chan, AYW; Lam, CW20135
Electronic chemical pathology consultation service and dried blood spot metabolic screening in hospital patients
Journal of Clinical Pathology
BMJ Publishing Group. The Journal's web site is located at
Mak, CM; Siu, WK; Law, CY; Wong, CK; Lee, HK; Yeung, S; Sham, CO; Tse, K; Lee, HHC; Chen, SPL; Ching, CK; Au, CK; Poon, WT; Lam, CW; Kwong, NS; Chan, AYW2012150
In search of the diagnosis, and the patient: transient galactosemia demystified after 14 years
Genetic Counseling
Editions Medecine et Hygiene. The Journal's web site is located at
Lee, HHC; Lam, CW; Yuen, YP; Lai, CK; Chan, KY; Chan, AYW201294
Young-onset Parkinsonism in a Hong Kong Chinese man with adult-onset Hallervorden-Spatz syndrome
International Journal of Neuroscience
Informa Healthcare. The Journal's web site is located at
Mak, CM; Sheng, B; Lee, HHC; Lau, KK; Chan, WT; Lam, CW; Chan, YW2011231
A novel duplication at the putative DNA polymerase alpha arrest site and a founder mutation in Chinese in the IVD gene underlie isovaleric acidaemia
Hong Kong Medical Journal
Hong Kong Medical Association. The Journal's web site is located at
Lee, HHC; Lee, RSY; Lai, CK; Yuen, YP; Siu, TS; Chan, AYW; Lam, CW2010315
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