Siu TS - Search Results

1

Fatal viral infection-associated encephalopathy in two Chinese boys: a genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants.

Mak CM, Lam CW, Fong NC, Siu WK, Lee HC, Siu TS, Lai CK, Law CY, Tong SF, Poon WT, Lam DS, Ng HL, Yuen YP, Tam S, Que TL, Kwong NS, Chan AY. Mak CM, et al. Among authors: siu ts, siu wk. J Hum Genet. 2011 Aug;56(8):617-21. doi: 10.1038/jhg.2011.63. Epub 2011 Jun 23. J Hum Genet. 2011. PMID: 21697855

2

Novel mutations in myopathic form of carnitine palmitoyltransferase II deficiency in a Chinese patient.

Cho SY, Siu TS, Ma O, Tam S, Lam CW. Cho SY, et al. Among authors: siu ts. Clin Chim Acta. 2013 Oct 21;425:125-7. doi: 10.1016/j.cca.2013.07.018. Epub 2013 Aug 1. Clin Chim Acta. 2013. PMID: 23911907

3

Role of postmortem genetic testing demonstrated in a case of glutaric aciduria type II.

Lee HC, Lai CK, Siu TS, Yuen YP, Chan KY, Chan AY, Tam S, Mak CM, Lam CW. Lee HC, et al. Among authors: siu ts. Diagn Mol Pathol. 2010 Sep;19(3):184-6. doi: 10.1097/PDM.0b013e3181c9a8a8. Diagn Mol Pathol. 2010. PMID: 20736750

4

Analysis of inborn errors of metabolism: disease spectrum for expanded newborn screening in Hong Kong.

Lee HC, Mak CM, Lam CW, Yuen YP, Chan AO, Shek CC, Siu TS, Lai CK, Ching CK, Siu WK, Chen SP, Law CY, Tai HL, Tam S, Chan AY. Lee HC, et al. Among authors: siu ts, siu wk. Chin Med J (Engl). 2011 Apr;124(7):983-9. Chin Med J (Engl). 2011. PMID: 21542954

5

Non-invasive urinary screening for aromatic L-amino acid decarboxylase deficiency in high-prevalence areas: a pilot study.

Lee HC, Lai CK, Yau KC, Siu TS, Mak CM, Yuen YP, Chan KY, Tam S, Lam CW, Chan AY. Lee HC, et al. Among authors: siu ts. Clin Chim Acta. 2012 Jan 18;413(1-2):126-30. doi: 10.1016/j.cca.2011.09.008. Epub 2011 Sep 21. Clin Chim Acta. 2012. PMID: 21963339

6

Molecular diagnosis for a fatal case of very long-chain acyl-CoA dehydrogenase deficiency in Hong Kong Chinese with a novel mutation: a preventable death by newborn screening.

Siu WK, Mak CM, Siu SL, Siu TS, Pang CY, Lam CW, Kwong NS, Chan AY. Siu WK, et al. Among authors: siu sl, siu ts. Diagn Mol Pathol. 2012 Sep;21(3):184-7. doi: 10.1097/PDM.0b013e31825554d0. Diagn Mol Pathol. 2012. PMID: 22847164

7

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.

Mak CM, Lam CW, Chim S, Siu TS, Ng KF, Tam S. Mak CM, et al. Among authors: siu ts. Clin Biochem. 2013 Jan;46(1-2):155-9. doi: 10.1016/j.clinbiochem.2012.09.010. Epub 2012 Sep 18. Clin Biochem. 2013. PMID: 23000314

8

Persistently increased acetaminophen concentrations in a patient with acute liver failure.

Fong BM, Siu TS, Tam S. Fong BM, et al. Among authors: siu ts. Clin Chem. 2011 Jan;57(1):9-11. doi: 10.1373/clinchem.2010.144527. Clin Chem. 2011. PMID: 21189276 No abstract available.

9

Metformin-associated lactic acidosis in Chinese patients with type II diabetes.

Yeung CW, Chung HY, Fong BM, Tsai NW, Chan WM, Siu TS, Tam S, Tsui SH. Yeung CW, et al. Among authors: siu ts. Pharmacology. 2011;88(5-6):260-5. doi: 10.1159/000331867. Epub 2011 Oct 13. Pharmacology. 2011. PMID: 21996640

10

Arginase deficiency with new phenotype and a novel mutation: contemporary summary.

Tsang JP, Poon WL, Luk HM, Fung CW, Ching CK, Mak CM, Lam CW, Siu TS, Tam S, Wong VC. Tsang JP, et al. Among authors: siu ts. Pediatr Neurol. 2012 Oct;47(4):263-9. doi: 10.1016/j.pediatrneurol.2012.06.012. Pediatr Neurol. 2012. PMID: 22964440

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