Yeung WL - Search Results

1

Telemedicine conference on a 13-year-old Chinese girl with an unusual skeletal condition.

Hui J, Yeung WL, Wong G, Fok TF, Griffith J, Cheng JC, Hjelm M, Hall C, Shaw D. Hui J, et al. Among authors: yeung wl. J Telemed Telecare. 1998;4(2):120-1. doi: 10.1258/1357633981931957. J Telemed Telecare. 1998. PMID: 9744169 No abstract available.

2

An infant with encephalitis.

Yeung WL, Ip M, Ng HK, Fok TF. Yeung WL, et al. Lancet. 1997 Nov 29;350(9091):1594. doi: 10.1016/s0140-6736(97)09514-7. Lancet. 1997. PMID: 9393339 No abstract available.

3

A Chinese girl with Leigh syndrome: effect of botulinum toxin on dystonia.

Leung TF, Hui J, Yeung WL, Goh K. Leung TF, et al. Among authors: yeung wl. J Paediatr Child Health. 1998 Oct;34(5):480-2. doi: 10.1046/j.1440-1754.1998.00275.x. J Paediatr Child Health. 1998. PMID: 9767517

4

Aplastic anaemia in association with Kearns-Sayre syndrome.

Leung TF, Hui J, Shoubridge E, Li CK, Chik KW, Shing MM, Wong GW, Yeung WL, Yuen PM. Leung TF, et al. Among authors: yeung wl. J Inherit Metab Dis. 1999 Feb;22(1):86-7. doi: 10.1023/a:1005415802893. J Inherit Metab Dis. 1999. PMID: 10070624 No abstract available.

5

Recurrent and novel mutations of GCDH gene in Chinese glutaric acidemia type I families.

Tang NL, Hui J, Law LK, Lam YY, Chan KY, Yeung WL, Chan AY, Cheung KL, Fok TF. Tang NL, et al. Among authors: yeung wl. Hum Mutat. 2000 Nov;16(5):446. doi: 10.1002/1098-1004(200011)16:5<446::AID-HUMU14>3.0.CO;2-Y. Hum Mutat. 2000. PMID: 11058907

6

Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.

Lam CW, Yeung WL, Ko CH, Poon PM, Tong SF, Chan KY, Lo IF, Chan LY, Hui J, Wong V, Pang CP, Lo YM, Fok TF. Lam CW, et al. Among authors: yeung wl. J Med Genet. 2000 Dec;37(12):E41. doi: 10.1136/jmg.37.12.e41. J Med Genet. 2000. PMID: 11106359 Free PMC article. No abstract available.

7

Red eyes as the initial presentation of systemic meningococcal infection.

Yeung WL, Yam KL, Chan WM, Hui J. Yeung WL, et al. J Paediatr Child Health. 2003 Jul;39(5):390-1. doi: 10.1046/j.1440-1754.2003.00161.x. J Paediatr Child Health. 2003. PMID: 12887674

8

Early-onset primary torsional dystonia in a 4-generation Chinese family with a mutation in the DYT1 gene.

Yeung WL, Lam CW, Cheng WT, Sin NC, Wong WK, Wong CN, Tse KM, Fok TF. Yeung WL, et al. Chin Med J (Engl). 2005 May 20;118(10):873-6. Chin Med J (Engl). 2005. PMID: 15989773 No abstract available.

9

Galactorrhea-a strong clinical clue towards the diagnosis of neurotransmitter disease.

Yeung WL, Lam CW, Hui J, Tong SF, Wu SP. Yeung WL, et al. Brain Dev. 2006 Jul;28(6):389-91. doi: 10.1016/j.braindev.2005.10.012. Epub 2006 Jan 10. Brain Dev. 2006. PMID: 16376043

10

Risk of vitamin A toxicity from candy-like chewable vitamin supplements for children.

Lam HS, Chow CM, Poon WT, Lai CK, Chan KC, Yeung WL, Hui J, Chan AY, Ng PC. Lam HS, et al. Among authors: yeung wl. Pediatrics. 2006 Aug;118(2):820-4. doi: 10.1542/peds.2006-0167. Pediatrics. 2006. PMID: 16882846

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