Cheng TS - Search Results

1

An epidemiological study of motor neuron disease in Hong Kong.

Fong GC, Cheng TS, Lam K, Cheng WK, Mok KY, Cheung CM, Chim CS, Mak W, Chan KH, Tsang KL, Kwan MC, Tsoi TH, Cheung RT, Ho SL. Fong GC, et al. Among authors: cheng ts, cheng wk. Amyotroph Lateral Scler Other Motor Neuron Disord. 2005 Sep;6(3):164-8. doi: 10.1080/14660820510028412a. Amyotroph Lateral Scler Other Motor Neuron Disord. 2005. PMID: 16247937

2

A prevalence study of epilepsy in Hong Kong.

Fong GC, Mak W, Cheng TS, Chan KH, Fong JK, Ho SL. Fong GC, et al. Among authors: cheng ts. Hong Kong Med J. 2003 Aug;9(4):252-7. Hong Kong Med J. 2003. PMID: 12904612 Free article.

3

Bath-related headache.

Mak W, Tsang KL, Tsoi TH, Au Yeung KM, Chan KH, Cheng TS, Cheung TF, Ho SL. Mak W, et al. Among authors: cheng ts. Cephalalgia. 2005 Mar;25(3):191-8. doi: 10.1111/j.1468-2982.2004.00832.x. Cephalalgia. 2005. PMID: 15689194

4

Clinical phenotypes of a large Chinese multigenerational kindred with autosomal dominant familial ALS due to Ile149Thr SOD1 gene mutation.

Fong GC, Kwok KH, Song YQ, Cheng TS, Ho PW, Chu AC, Kung MH, Chan KH, Mak W, Cheung RT, Ramsden DB, Ho SL. Fong GC, et al. Among authors: cheng ts. Amyotroph Lateral Scler. 2006 Sep;7(3):142-9. doi: 10.1080/17482960600732412. Amyotroph Lateral Scler. 2006. PMID: 16963403

5

Wilson's disease with depression and parkinsonism.

Chan KH, Cheung RT, Au-Yeung KM, Mak W, Cheng TS, Ho SL. Chan KH, et al. Among authors: cheng ts. J Clin Neurosci. 2005 Apr;12(3):303-5. doi: 10.1016/j.jocn.2004.09.005. J Clin Neurosci. 2005. PMID: 15851088

6

A possible explanation for the racial difference in distribution of large-arterial cerebrovascular disease: ancestral European settlers evolved genetic resistance to atherosclerosis, but confined to the intracranial arteries.

Mak W, Cheng TS, Chan KH, Cheung RT, Ho SL. Mak W, et al. Among authors: cheng ts. Med Hypotheses. 2005;65(4):637-48. doi: 10.1016/j.mehy.2005.05.017. Med Hypotheses. 2005. PMID: 16006051

7

Cerebrospinal fluid to serum glucose ratio in non-hypoglycorrhachic neurological conditions.

Mak W, Cheng TS, Chan KH, Cheung RT, Ho SL. Mak W, et al. Among authors: cheng ts. Hong Kong Med J. 2005 Dec;11(6):457-62. Hong Kong Med J. 2005. PMID: 16340022 Free article.

8

Myopia as a latent phenotype of a pleiotropic gene positively selected for facilitating neurocognitive development, and the effects of environmental factors in its expression.

Mak W, Kwan MW, Cheng TS, Chan KH, Cheung RT, Ho SL. Mak W, et al. Among authors: cheng ts. Med Hypotheses. 2006;66(6):1209-15. doi: 10.1016/j.mehy.2005.11.037. Epub 2006 Jan 18. Med Hypotheses. 2006. PMID: 16413689

9

-459C>T point mutation in 5' non-coding region of human GJB1 gene is linked to X-linked Charcot-Marie-Tooth neuropathy.

Li M, Cheng TS, Ho PW, Chan KH, Mak W, Cheung RT, Ramsden DB, Sham PC, Song Y, Ho SL. Li M, et al. Among authors: cheng ts. J Peripher Nerv Syst. 2009 Mar;14(1):14-21. doi: 10.1111/j.1529-8027.2009.00201.x. J Peripher Nerv Syst. 2009. PMID: 19335535

10

Abnormal diffusion tensor in nonsymptomatic familial amyotrophic lateral sclerosis with a causative superoxide dismutase 1 mutation.

Ng MC, Ho JT, Ho SL, Lee R, Li G, Cheng TS, Song YQ, Ho PW, Fong GC, Mak W, Chan KH, Li LS, Luk KD, Hu Y, Ramsden DB, Leong LL. Ng MC, et al. Among authors: cheng ts. J Magn Reson Imaging. 2008 Jan;27(1):8-13. doi: 10.1002/jmri.21217. J Magn Reson Imaging. 2008. PMID: 18022844

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