Law LK - Search Results

1

The role of spatial structure in at-risk metapopulation recoveries.

Wilson KL, Sawyer AC, Potapova A, Bailey CJ, LoScerbo D, Sweeney-Bergen EK, Hodgson EE, Pitman KJ, Seitz KM, Law LK, Warkentin L, Wilson SM, Atlas WI, Braun DC, Sloat MR, Tinker MT, Moore JW. Wilson KL, et al. Among authors: law lk. Ecol Appl. 2023 Sep;33(6):e2898. doi: 10.1002/eap.2898. Epub 2023 Jun 29. Ecol Appl. 2023. PMID: 37303288

2

Causes and prognosis of symptomatic pericardial effusions treated by pericardiocentesis in an Asian academic medical centre.

Cheong XP, Law LKP, Seow SC, Tay LWE, Tan HC, Yeo WT, Low AF, Kojodjojo P. Cheong XP, et al. Among authors: law lkp. Singapore Med J. 2020 Mar;61(3):137-141. doi: 10.11622/smedj.2019065. Epub 2019 Jul 11. Singapore Med J. 2020. PMID: 32488274 Free PMC article.

3

Expanded newborn metabolic screening programme in Hong Kong: a three-year journey.

Chong SC, Law LK, Hui J, Lai CY, Leung TY, Yuen YP. Chong SC, et al. Among authors: law lk. Hong Kong Med J. 2017 Oct;23(5):489-96. doi: 10.12809/hkmj176274. Epub 2017 Sep 1. Hong Kong Med J. 2017. PMID: 28862145 Free article.

4

One too many: intellectual disability secondary to undiagnosed phenylketonuria.

Hui J, Chong SC, Law LK, Lee LK, Chang S, Yau P, Yuen YP. Hui J, et al. Among authors: law lk. Hong Kong Med J. 2016 Oct;22(5):506-8. doi: 10.12809/hkmj144500. Hong Kong Med J. 2016. PMID: 27738300 Free article. No abstract available.

5

Inherited metabolic diseases in the Southern Chinese population: spectrum of diseases and estimated incidence from recurrent mutations.

Hui J, Tang NL, Li CK, Law LK, To KF, Yau P, Fung SL, Chong JS, Tsung L, Chiang G, Fung E, Cheung KL, Yeung WL, Fok TF. Hui J, et al. Among authors: law lk. Pathology. 2014 Aug;46(5):375-82. doi: 10.1097/PAT.0000000000000140. Pathology. 2014. PMID: 24992243 Review.

6

A novel ALDH5A1 mutation in a patient with succinic semialdehyde dehydrogenase deficiency.

Kwok JS, Yuen CL, Law LK, Tang NL, Cherk SW, Yuen YP. Kwok JS, et al. Among authors: law lk. Pathology. 2012 Apr;44(3):280-2. doi: 10.1097/PAT.0b013e32835140c2. Pathology. 2012. PMID: 22437753 No abstract available.

7

Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.

Law LK, Tang NL, Hui J, Fung SL, Ruiter J, Wanders RJ, Fok TF, Lam CW. Law LK, et al. Clin Chim Acta. 2009 Jun 27;404(2):95-9. doi: 10.1016/j.cca.2009.02.015. Epub 2009 Mar 3. Clin Chim Acta. 2009. PMID: 19265687

8

Electrospray ionisation mass spectrometry: principles and clinical applications.

Ho CS, Lam CW, Chan MH, Cheung RC, Law LK, Lit LC, Ng KF, Suen MW, Tai HL. Ho CS, et al. Among authors: law lk. Clin Biochem Rev. 2003;24(1):3-12. Clin Biochem Rev. 2003. PMID: 18568044 Free PMC article.

9

Deficiency of the carnitine transporter (OCTN2) with partial N-acetylglutamate synthase (NAGS) deficiency.

Hwu WL, Chien YH, Tang NL, Law LK, Lin CY, Lee NC. Hwu WL, et al. Among authors: law lk. J Inherit Metab Dis. 2007 Oct;30(5):816. doi: 10.1007/s10545-007-0594-y. Epub 2007 Aug 20. J Inherit Metab Dis. 2007. PMID: 17703373

10

A novel functional assay for simultaneous determination of total fatty acid beta-oxidation flux and acylcarnitine profiling in human skin fibroblasts using (2)H(31)-palmitate by isotope ratio mass spectrometry and electrospray tandem mass spectrometry.

Law LK, Tang NL, Hui J, Ho CS, Ruiter J, Fok TF, Wanders RJ, Lam CW. Law LK, et al. Clin Chim Acta. 2007 Jul;382(1-2):25-30. doi: 10.1016/j.cca.2007.03.011. Epub 2007 Mar 21. Clin Chim Acta. 2007. PMID: 17442290

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