| Title | Author(s) | Year | View Count |
 | Heterogeneous mutations of the ATP2C1 gene causing Hailey-Hailey disease in Hong Kong Chinese | Cheng, TS; Ho, KM; Lam, CW | 2010 | 199 |
| -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, PWL; Chan, KH; Mak, W; Cheung, RTF; Ramsden, DB; Sham, PC; Song, Y; Ho, SL | 2009 | 109 |
 | Generalisation in myasthenia gravis presenting with pure ocular symptoms | Pang, SYY; Ho, SL; Mak, W; Cheung, RTF; Cheng, TS; Tse, CT; Chang, SK; Chan, KH | 2009 | 114 |
| 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, PWL; Fong, GCY; Mak, W; Chan, KH; Li, LSW; Luk, KDK; Hu, Y; Ramsden, DB; Leong, LLY | 2008 | 223 |
| MR-DTI study: abnormal water diffusion pattern in asymptomatic familial amyotrophic lateral sclerosis with SOD1 mutation | Ng, MC; Ho, JT; Ho, SL; Lee, R; Li, G; Cheng, TS; Song, YQ; Kwok, HH; Ho, WL; Chu, CYA; Fong, CY; Chan, KH; Cheung, RTF; Li, LSW; Yang, ES; Luk, KDK; Hu, Y; Ramsden, DB; Leong Fung, LLY | 2007 | 121 |
| Clinical phenotypes of a large Chinese multigenerational kindred with autosomal dominant familial ALS due to Ile149Thr SOD1 gene mutation | Fong, GCY; Kwok, KHH; Song, YQ; Cheng, TS; Ho, PWL; Chu, ACY; Kung, MHW; Chan, KH; Mak, W; Cheung, RTF; Ramsden, DB; Ho, SL | 2006 | 124 |
| 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, MWM; Cheng, TS; Chan, KH; Cheung, RTF; Ho, SL | 2006 | 53 |
| Muscle-specific kinase autoantibody in acetylcholine receptor antibody-negative generalized acquired myasthenia gravis | Chan, KH; Mak, W; Cheung, RTF; Cheng, TS; Ho, SL | 2006 | 80 |
| Wilson's disease with depression and parkinsonism | Chan, KH; Cheung, RTF; AuYeung, KM; Mak, W; Cheng, TS; Ho, SL | 2005 | 115 |
| 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, RTF; Ho, SL | 2005 | 108 |
| Bath-related headache | Mak, W; Tsang, KL; Tsoi, TH; Au Yeung, KM; Chan, KH; Cheng, TS; Cheung, TFR; Ho, SL | 2005 | 157 |
| An epidemiological study of motor neuron disease in Hong Kong | Fong, GCY; Cheng, TS; Lam, K; Cheng, WK; Mok, KY; Cheung, CM; Chim, CS; Mak, W; Chan, KH; Tsang, KL; Kwan, MC; Tsoi, TH; Cheung, RTF; Ho, SL | 2005 | 81 |
| Cerebellar degeneration and folate deficiency due to cough misture abuse | Au, WY; Cheng, TS; Siu, TS; Yuen, KY | 2005 | 100 |
| Clinical outcome between early and late settlement of high blood pressure in acute intracerebral haemorrhage | Cheng, TS; Cheung, RTF; Ho, SL | 2005 | 83 |
| Clinical relevancy of severe initial hypertension in acute intracerebral haemorrhage | Cheng, TS; Cheung, RTF; Ho, SL | 2005 | 67 |
| Cerebrospinal fluid to serum glucose ratio in non-hypoglycorrhachic neurological conditions. | Mak, W; Cheng, TS; Chan, KH; Cheung, RTF; Ho, SL | 2005 | 76 |
 | Cerebrospinal fluid to serum glucose ratio in non-hypoglycorrhachic neurological conditions | Mak, W; Cheng, TS; Chan, KH; Cheung, RTF; Ho, SL | 2005 | 278 |
| Predictive factors for ischemic strokes complicating tuberculous meningitis | Chan, KH; Cheung, RTF; Mak, W; Fong, CYG; Tsang, KL; Cheng, TS; Ho, SL | 2004 | 136 |
| Clinical relevance of severe initial hypertension in acute intracerebral haemorrhage | Cheng, TS; Mak, W; Fong, GCY; Chan, KH; Ho, SL; Cheung, RTF | 2004 | 137 |
| Clinical relevance of severe initial hypertension in acute intracerebral haemorrhage. | Cheng, TS; Mak, W; Fong, CY; Chan, KH; Ho, SL; Cheung, RTF | 2004 | 63 |
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