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Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|September 2, 2017
Expanded newborn metabolic screening programme in Hong Kong: a three-year journeyS C Chong, L K Law, J Hui, et al.
Clinical Chemistry|December 4, 1998
Routine analysis of plasma busulfan by gas chromatography-mass fragmentographyW K Lai, C P Pang, L K Law, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 5, 1998
Rarity of debrisoquine hydroxylase gene polymorphism in Chinese patients with Parkinson's diseaseC P Pang, J Zhang, J Woo, et al.
Human Mutation|August 31, 2002
A founder mutation (R254X) of SLC22A5 (OCTN2) in Chinese primary carnitine deficiency patientsNelson L S Tang, W L Hwu, Rachel T Chan, et al.
Journal of Inherited Metabolic Disease|August 19, 2007
Deficiency of the carnitine transporter (OCTN2) with partial N-acetylglutamate synthase (NAGS) deficiencyW-L Hwu, Y-H Chien, N L S Tang, et al.
Journal of Human Hypertension|June 1, 1994
Atrial natriuretic peptide and renin-angiotensin-aldosterone system in non-insulin-dependent diabetes mellitusJ C Chan, C K Cheung, C S Cockram, et al.
Hong Kong Medical Journal = Xianggang Yi Xue Za Zhi|June 11, 2002
Primary hyperoxaluria: a rare but important cause of nephrolithiasisP N Wong, G M W Tong, K Y Lo, et al.
Peritoneal Dialysis International : Journal of the International Society for Peritoneal Dialysis|December 6, 2007
Diagnosis of primary hyperoxaluria type 1 by determination of peritoneal dialysate glycolic acid using standard organic-acids analysis methodPing-Nam Wong, Eric L K Law, Gensy M W Tong, et al.
Human Reproduction (Oxford, England)|June 4, 2002
Follicular fluid and serum concentrations of myo-inositol in patients undergoing IVF: relationship with oocyte qualityTony T Y Chiu, Michael S Rogers, Eric L K Law, et al.
Journal of Paediatrics and Child Health|February 13, 2001
Normal pulse oximeter reading in a cyanotic infantA M Li, W Wong, M H Chan, et al.
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