Yuen YP - Search Results

1

Chan AO, Lam CW, Tong SF, Cheng MT, Yung K, Chan YW, Au KM, Yuen YP, Hung CT, Ng KP, Shek CC. Chan AO, et al. Among authors: yuen yp. Hum Genet. 2007 Apr;121(2):288. Hum Genet. 2007. PMID: 17598201 No abstract available.

2

Novel mutations in the BCHE gene in patients with no butyrylcholinesterase activity.

On-Kei Chan A, Lam CW, Tong SF, Man Tung C, Yung K, Chan YW, Au KM, Yuen YP, Hung CT, Ng KP, Shek CC. On-Kei Chan A, et al. Among authors: yuen yp. Clin Chim Acta. 2005 Jan;351(1-2):155-9. doi: 10.1016/j.cccn.2004.09.004. Clin Chim Acta. 2005. PMID: 15563885

3

Gene symbol: BCHE.

Chan AO, Lam CW, Tong SF, Tung CM, Yung K, Chan YW, Au KM, Yuen YP, Hung CT, Ng KP, Shek CC. Chan AO, et al. Among authors: yuen yp. Hum Genet. 2007 Apr;121(2):289. Hum Genet. 2007. PMID: 17598228 No abstract available.

4

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. Among authors: yuen yp. Mol Genet Metab. 2002 Jan;75(1):91-5. doi: 10.1006/mgme.2001.3267. Mol Genet Metab. 2002. PMID: 11825068

5

Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b.

Yuen YP, Cheng WF, Tong SF, Chan YT, Chan YW, Lam CW. Yuen YP, et al. Mol Genet Metab. 2002 Nov;77(3):249-51. doi: 10.1016/s1096-7192(02)00110-5. Mol Genet Metab. 2002. PMID: 12409273

6

Ethnic-specific splicing mutation of the carnitine-acylcarnitine translocase gene in a Chinese neonate presenting with sudden unexpected death.

Lam CW, Lai CK, Chow CB, Tong SF, Yuen YP, Mak YF, Chan YW. Lam CW, et al. Among authors: yuen yp. Chin Med J (Engl). 2003 Jul;116(7):1110-2. Chin Med J (Engl). 2003. PMID: 12890396 No abstract available.

7

Missense mutation Leu72Pro located on the carboxyl terminal amphipathic helix of apolipoprotein C-II causes familial chylomicronemia syndrome.

Lam CW, Yuen YP, Cheng WF, Chan YW, Tong SF. Lam CW, et al. Among authors: yuen yp. Clin Chim Acta. 2006 Feb;364(1-2):256-9. doi: 10.1016/j.cca.2005.07.025. Epub 2005 Sep 8. Clin Chim Acta. 2006. PMID: 16153625

8

WITHDRAWN: Novel missense mutation (Y24H) in the G6PT1 gene causing glycogen storage disease type 1b.

Yuen YP, Cheng WF, Tong SF, Chan YT, Chan YW, Lam CW. Yuen YP, et al. Mol Genet Metab. 2009 Mar 23. doi: 10.1016/S1096-7192(02)00057-4. Online ahead of print. Mol Genet Metab. 2009. PMID: 19321372

9

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: yuen yp. 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

10

Diagnosis of dihydropyrimidine dehydrogenase deficiency in a neonate with thymine-uraciluria.

Au KM, Lai CK, Yuen YP, Shek CC, Lam CW, Chan AY. Au KM, et al. Among authors: yuen yp. Hong Kong Med J. 2003 Apr;9(2):130-2. Hong Kong Med J. 2003. PMID: 12668826 Free article.

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

57 results

Search Page

Filters