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Showing results 1 to 11 of 11

	Title	Author(s)	Issue Date
	2,4-Dinitrophenol: A threat to Chinese body-conscious groups Journal:Journal of the Chinese Medical Association	Lee, HHC Law, CY Chen, ML Lam, YH Chan, AY Mak, TW	2014
	Cost-benefit analysis of Hyperphenylalaninemia Due to 6-Pyruvoyl-Tetrahydropterin Synthase (PTPS) Deficiency: For Consideration of Expanded Newborn Screening in Hong Kong Journal:Journal of Medical Screening	Lee, HHC Mak, CM Poon, WKG Wong, KY Lam, CW	2014
	Electronic chemical pathology consultation service and dried blood spot metabolic screening in hospital patients Journal:Journal of Clinical Pathology	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, AYW	2012
	Federated deep learning for detecting COVID-19 lung abnormalities in CT: a privacy-preserving multinational validation study Journal:npj Digital Medicine	Dou, Q So, TY Jiang, M Liu, Q Vardhanabhuti, V Kaissis, G Li, Z Si, W Lee, HHC Yu, K Feng, Z Dong, L Burian, E Jungmann, F Braren, R Makowski, M Kainz, B Rueckert, D Glocker, B Yu, SCH Heng, PA	2021
	Genetic basis of channelopathies and cardiomyopathies in Hong Kong Chinese patients: a 10-year regional laboratory experience Journal:Hong Kong Medical Journal	Mak, CM Chen, SPL Mok, NS Siu, WK Lee, HHC Ching, DCK Tsui, PT Fong, NC Yuen, YP Poon, DWT Law, CY Chong, YK Chan, YW Yung, TC Fan, KY Lam, CW	2018
	Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome: a treatable genetic liver disease warranting urgent diagnosis Journal:Hong Kong Medical Journal	Lee, HHC Poon, KH Lai, CK Au, KM Siu, TS Lai, JPS Mak, CM Yuen, LYP Lam, CW Chan, AYW	2014
	In search of the diagnosis, and the patient: transient galactosemia demystified after 14 years Journal:Genetic Counseling	Lee, HHC Lam, CW Yuen, YP Lai, CK Chan, KY Chan, AYW	2012
	Inborn errors of metabolism and expanded newborn screening: review and update Journal:Critical Reviews in Clinical Laboratory Sciences	Mak, CM Lee, HHC Chan, AYW Lam, CW	2013
	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, HHC Lee, RSY Lai, CK Yuen, YP Siu, TS Chan, AYW Lam, CW	2010
	Novel POLG mutation in a patient with sensory ataxia, neuropathy, ophthalmoparesis and stroke Journal:Clinica Chimica Acta	Lam, CW Law, CY Siu, CWK Fung, CW Yau, MM Huen, KF Lee, HHC Mak, CM	2015
	Young-onset Parkinsonism in a Hong Kong Chinese man with adult-onset Hallervorden-Spatz syndrome Journal:International Journal of Neuroscience	Mak, CM Sheng, B Lee, HHC Lau, KK Chan, WT Lam, CW Chan, YW	2011

Showing results 1 to 11 of 11