Mak CM - Search Results

1

The first pilot study of expanded newborn screening for inborn errors of metabolism and survey of related knowledge and opinions of health care professionals in Hong Kong.

Mak CM, Law EC, Lee HH, Siu WK, Chow KM, Au Yeung SK, Ngan HY, Tse NK, Kwong NS, Chan GC, Lee KW, Chan WP, Wong SF, Tang MH, Kan AS, Hui AP, So PL, Shek CC, Lee RS, Wong KY, Yau EK, Poon KH, Siu S, Poon GW, Kwok AM, Ng JW, Yim VC, Ma GG, Chu CH, Tong TY, Chong YK, Chen SP, Ching CK, Chan AO, Tam S, Lau RL, Ng WF, Lee KC, Chan AY, Lam CW. Mak CM, et al. Hong Kong Med J. 2018 Jun;24(3):226-237. doi: 10.12809/hkmj176939. Epub 2018 Jun 4. Hong Kong Med J. 2018. PMID: 29888706 Free article.

2

Genetics of familial amyloidotic polyneuropathy in a Hong Kong Chinese kindred.

Mak CM, Lam CW, Fan ST, Liu CL, Tam SC. Mak CM, et al. Acta Neurol Scand. 2003 Jun;107(6):419-22. doi: 10.1034/j.1600-0404.2003.00047.x. Acta Neurol Scand. 2003. PMID: 12757474

3

A case of 'crouching' triglyceride and 'hidden' cholesterol.

Mak CM, Pang RW, Tam S. Mak CM, et al. Br J Biomed Sci. 2004;61(3):152-3. doi: 10.1080/09674845.2004.11978137. Br J Biomed Sci. 2004. PMID: 15462264 No abstract available.

4

Serial lipoprotein electrophoresis reveals the lipid changes in L-asparaginase-induced chylomicronaemia syndrome.

Mak CM, Pang RW, Chan GC, Wong WK, Tam S. Mak CM, et al. Br J Biomed Sci. 2005;62(2):95-7. Br J Biomed Sci. 2005. PMID: 15997887 No abstract available.

5

Wilson's disease: a patient undiagnosed for 18 years.

Mak CM, Tam S, Fan ST, Liu CL, Lam CW. Mak CM, et al. Hong Kong Med J. 2006 Apr;12(2):154-8. Hong Kong Med J. 2006. PMID: 16603785 Free article. Review.

6

Complete recovery from acute encephalopathy of late-onset ornithine transcarbamylase deficiency in a 3-year-old boy.

Mak CM, Siu TS, Lam CW, Chan GC, Poon GW, Wong KY, Low LC, Tang NL, Li SK, Lau KY, Kwong NS, Tam S. Mak CM, et al. J Inherit Metab Dis. 2007 Nov;30(6):981. doi: 10.1007/s10545-007-0692-x. Epub 2007 Oct 5. J Inherit Metab Dis. 2007. PMID: 17922216

7

Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese.

Mak CM, Lam CW, Siu TS, Chan KY, Siu WK, Yeung WL, Hui J, Wong VC, Low LC, Ko CH, Fung CW, Chen SP, Yuen YP, Lee HC, Yau E, Chan B, Tong SF, Tam S, Chan YW. Mak CM, et al. Mol Genet Metab. 2010 Apr;99(4):431-3. doi: 10.1016/j.ymgme.2009.12.011. Epub 2009 Dec 21. Mol Genet Metab. 2010. PMID: 20056467

8

RYR1-related central core myopathy in a Chinese adolescent boy.

Chan B, Chen SP, Wong WC, Mak CM, Wong S, Chan KY, Chan AY. Chan B, et al. Among authors: mak cm. Hong Kong Med J. 2011 Feb;17(1):67-70. Hong Kong Med J. 2011. PMID: 21282829 Free article.

9

BAG3-related myofibrillar myopathy in a Chinese family.

Lee HC, Cherk SW, Chan SK, Wong S, Tong TW, Ho WS, Chan AY, Lee KC, Mak CM. Lee HC, et al. Among authors: mak cm. Clin Genet. 2012 Apr;81(4):394-8. doi: 10.1111/j.1399-0004.2011.01659.x. Epub 2011 Apr 4. Clin Genet. 2012. PMID: 21361913

10

Hypoglycaemia due to autoimmune insulin syndrome in a 78-year-old Chinese man.

Yeung CW, Mak CM, Lam KS, Tam S. Yeung CW, et al. Among authors: mak cm. Br J Biomed Sci. 2012;69(2):80-2. Br J Biomed Sci. 2012. PMID: 22872933 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

133 results

Search Page

Filters