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Tak-Shing Siu

Observed names: T S Siu, T. S. Siu, T.-S. Siu, T.S. Siu, T.‐S. Siu, Tak-Shing S. Siu, Tak-shing Siu
Institution: Queen Mary Hospital
OpenAlex ID: A5113678460
Determination of Mercury in Whole Blood and Urine by Inductively Coupled Plasma Mass Spectrometry
2007 · B. M. W. Fong, T. S. Siu, et al. · Journal of Analytical Toxicology · 230
Analysis of Melamine Cyanurate in Urine Using Matrix-Assisted Laser Desorption/Ionization Mass Spectrometry
2009 · Ho-Wai Tang, Kwan-Ming Ng, et al. · Analytical Chemistry · 70
Fatal viral infection-associated encephalopathy in two Chinese boys: a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants
2011 · Chloe Miu Mak, Ching-wan Lam, et al. · Journal of Human Genetics · 38
The variability of the hepatitis B virus genome: statistical analysis and biological implications.
1993 · I J Lauder, H J Lin, et al. · Molecular Biology and Evolution · 32
Lathosterolosis: A Disorder of Cholesterol Biosynthesis Resembling Smith-Lemli-Opitz Syndrome
2013 · A. C. C. Ho, C. W. Fung, et al. · JIMD Reports · 27
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Non-invasive urinary screening for aromatic l-amino acid decarboxylase deficiency in high-prevalence areas: A pilot study
2011 · Han-Chih Hencher Lee, Chi-Kong Lai, et al. · Clinica Chimica Acta · 22
Fumarylacetoacetate Hydrolase Knock-out Rabbit Model for Hereditary Tyrosinemia Type 1
2017 · Li Li, Quanjun Zhang, et al. · Journal of Biological Chemistry · 19
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Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese
2009 · C.M. Mak, C.W. Lam, et al. · Molecular Genetics and Metabolism · 18
Biochemical and molecular diagnosis of tyrosinemia type I with two novel FAH mutations in a Hong Kong chinese patient: Recommendation for expanded newborn screening in Hong Kong
2012 · Chloe Miu Mak, Ching-wan Lam, et al. · Clinical Biochemistry · 16
Role of Postmortem Genetic Testing Demonstrated in a Case of Glutaric Aciduria Type II
2010 · Han-Chih Hencher Lee, Chi-Kong Lai, et al. · Diagnostic Molecular Pathology · 11
A novel duplication at the putative DNA polymerase alpha arrest site and a founder mutation in Chinese in the IVD gene underlie isovaleric acidaemia.
2010 · Hencher H C Lee, Robert S Y Lee, et al. · PubMed · 11
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Complete recovery from acute encephalopathy of late‐onset ornithine transcarbamylase deficiency in a 3‐year‐old boy
2007 · C. M. Mak, T.‐S. Siu, et al. · Journal of Inherited Metabolic Disease · 11
Quantitation of homoharringtonine in plasma by high-performance liquid chromatography with amperometric detection
1989 · Ying-Pui M. Chan, Foo-Wing Lee, et al. · Journal of Chromatography B Biomedical Sciences and Applications · 10
Cough mixture abuse as a novel cause of folate deficiency: a prospective, community-based, controlled study
2007 · W.-y. Au, S.-K. Tsang, et al. · Haematologica · 9
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Measurement of serum aldosterone in picomolar level by LC-MS/MS using charge-tagged technique
2015 · Bonnie Mei-Wah Fong, Tak-Shing Siu, et al. · Analytical and Bioanalytical Chemistry · 8
Molecular Diagnosis for a Fatal Case of Very Long-chain Acyl-CoA Dehydrogenase Deficiency in Hong Kong Chinese With a Novel Mutation
2012 · Wai-Kwan Siu, Chloe Miu Mak, et al. · Diagnostic Molecular Pathology · 7
DNA-based diagnosis of erythropoietic protoporphyria in two families and the frequency of a low-expression FECH allele in a Chinese population
2008 · Kin-Chong Lau, Ching-Wan Lam, et al. · Clinica Chimica Acta · 7
Cerebellar degeneration and folate deficiency due to cough mixture abuse.
2005 · W Y Au, T S Cheng, et al. · PubMed · 7
A novel mutation of SLC22A12 gene causing primary renal hypouricemia in a patient with metabolic syndrome
2008 · Ching-Wan Lam, Alice P.S. Kong, et al. · Clinica Chimica Acta · 6
Novel mutations in myopathic form of carnitine palmitoyltransferase II deficiency in a Chinese patient
2013 · Sun Young Cho, Tak-Shing Siu, et al. · Clinica Chimica Acta · 4
Congee: a cause of gross but transient elevation in plasma creatinine concentration
2011 · H.C.H. Lee, M.C. Mak, et al. · British Journal of Biomedical Science · 1
A novel mutation at a ligand-binding site of hypoxanthine–guanine phosphoribosyl transferase, p.Y105C (HPRTHongKong), in a Chinese teenager with recurrent gouty arthritis
2007 · Ching-Wan Lam, Kwok-Piu, Lee, et al. · Clinica Chimica Acta · 1
Biochemical and molecular characterization of dopa-responsive dystonias in Hong Kong Chinese
2010 · C.M. Mak, T.S. Siu, et al. · Clinica Chimica Acta
Modified clinical protocol for the investigations of dystonia: NON-INVASIVE Biochemical diagnosis of aromatic L-amino acid decarboxylase deficiency in Chinese
2010 · H.H.C. Lee, C.K. Lai, et al. · Clinica Chimica Acta
A sensitive method for measuring plasma catecholamines and its application on the study of the effect of alfentanil and esmolol on intra-operative hypertension
1998 · Tak-shing Siu
Works count: 25
Citation count: 565
H-index: 11
I10-index: 13
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