Lam CW - Search Results

1

Diagnostic yield of array CGH in patients with autism spectrum disorder in Hong Kong.

Siu WK, Lam CW, Mak CM, Lau ET, Tang MH, Tang WF, Poon-Mak RS, Lee CC, Hung SF, Leung PW, Kwong KL, Yau EK, Ng GS, Fong NC, Chan KY. Siu WK, et al. Among authors: lam cw. Clin Transl Med. 2016 Dec;5(1):18. doi: 10.1186/s40169-016-0098-1. Epub 2016 May 16. Clin Transl Med. 2016. PMID: 27271878 Free PMC article.

2

DNA-based diagnosis of isolated sulfite oxidase deficiency by denaturing high-performance liquid chromatography.

Lam CW, Li CK, Lai CK, Tong SF, Chan KY, Ng GS, Yuen YP, Cheng AW, Chan YW. Lam CW, et al. Mol Genet Metab. 2002 Jan;75(1):91-5. doi: 10.1006/mgme.2001.3267. Mol Genet Metab. 2002. PMID: 11825068

3

Allele dropout in PCR-based diagnosis of Wilson disease: mechanisms and solutions.

Lam CW, Mak CM. Lam CW, et al. Clin Chem. 2006 Mar;52(3):517-20. doi: 10.1373/clinchem.2005.060491. Clin Chem. 2006. PMID: 16510432

4

Cardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope.

Mok NS, Lam CW, Fong NC, Hui YW, Choi YC, Chan KY. Mok NS, et al. Among authors: lam cw. Chin Med J (Engl). 2006 Dec 20;119(24):2129-33. Chin Med J (Engl). 2006. PMID: 17199967 No abstract available.

5

Identification of a novel TTR Gly67Glu mutant and the first case series of familial transthyretin amyloidosis in Hong Kong Chinese.

Mak CM, Kwong YL, Lam CW, Chan SC, Lo CM, Fan ST, Chang CM, Lau YK, U LS, Tam S. Mak CM, et al. Among authors: lam cw. Amyloid. 2007 Dec;14(4):293-7. doi: 10.1080/13506120701616532. Amyloid. 2007. PMID: 17968690

6

Mutational analysis of 65 Wilson disease patients in Hong Kong Chinese: identification of 17 novel mutations and its genetic heterogeneity.

Mak CM, Lam CW, Tam S, Lai CL, Chan LY, Fan ST, Lau YL, Lai JY, Yuen P, Hui J, Fu CC, Wong KS, Mak WL, Tze K, Tong SF, Lau A, Leung N, Hui A, Cheung KM, Ko CH, Chan YK, Ma O, Chau TN, Chiu A, Chan YW. Mak CM, et al. Among authors: lam cw. J Hum Genet. 2008;53(1):55-63. doi: 10.1007/s10038-007-0218-2. Epub 2007 Nov 22. J Hum Genet. 2008. PMID: 18034201

7

Diagnostic accuracy of serum ceruloplasmin in Wilson disease: determination of sensitivity and specificity by ROC curve analysis among ATP7B-genotyped subjects.

Mak CM, Lam CW, Tam S. Mak CM, et al. Among authors: lam cw. Clin Chem. 2008 Aug;54(8):1356-62. doi: 10.1373/clinchem.2008.103432. Epub 2008 Jun 12. Clin Chem. 2008. PMID: 18556333

8

Diagnosis of Wilson's disease: a comprehensive review.

Mak CM, Lam CW. Mak CM, et al. Among authors: lam cw. Crit Rev Clin Lab Sci. 2008;45(3):263-90. doi: 10.1080/10408360801991055. Crit Rev Clin Lab Sci. 2008. PMID: 18568852 Review.

9

Rapid diagnosis of Wilson disease by a 28-mutation panel: real-time amplification refractory mutation system in diagnosing acute Wilsonian liver failure.

Mak CM, Lam CW, Lai ST, Hui Y, Tam S. Mak CM, et al. Among authors: lam cw. Clin Chim Acta. 2008 Dec;398(1-2):39-42. doi: 10.1016/j.cca.2008.08.002. Epub 2008 Aug 8. Clin Chim Acta. 2008. PMID: 18760268

10

A fast modified protocol for random-access ultra-high density whole-genome scan: a tool for personalized genomic medicine, positional mapping, and cytogenetic analysis.

Lau KC, Mak CM, Leung KY, Tsoi TH, Tang HY, Lee P, Lam CW. Lau KC, et al. Among authors: lam cw. Clin Chim Acta. 2009 Aug;406(1-2):31-5. doi: 10.1016/j.cca.2009.05.005. Epub 2009 May 13. Clin Chim Acta. 2009. PMID: 19445911

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