Results 1 to 20 of 43
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TypeTitleAuthor(s)YearViews
Heterogeneous mutations of the ATP2C1 gene causing Hailey-Hailey disease in Hong Kong ChineseCheng, TS; Ho, KM; Lam, CW2010194
 
Generalisation in myasthenia gravis presenting with pure ocular symptomsPang, SYY; Ho, SL; Mak, W; Cheung, RTF; Cheng, TS; Tse, CT; Chang, SK; Chan, KH2009112
 
-459C>T point mutation in 5′ non-coding region of human GJB1 gene is linked to X-linked Charcot-Marie-Tooth neuropathyLi, M; Cheng, TS; Ho, PWL; Chan, KH; Mak, W; Cheung, RTF; Ramsden, DB; Sham, PC; Song, Y; Ho, SL2009155
 
Abnormal diffusion tensor in nonsymptomatic familial amyotrophic lateral sclerosis with a causative superoxide dismutase 1 mutationNg, 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, LLY2008232
 
MR-DTI study: abnormal water diffusion pattern in asymptomatic familial amyotrophic lateral sclerosis with SOD1 mutationNg, 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, LLY2007106
 
Clinical phenotypes of a large Chinese multigenerational kindred with autosomal dominant familial ALS due to Ile149Thr SOD1 gene mutationFong, GCY; Kwok, KHH; Song, YQ; Cheng, TS; Ho, PWL; Chu, ACY; Kung, MHW; Chan, KH; Mak, W; Cheung, RTF; Ramsden, DB; Ho, SL2006121
 
Muscle-specific kinase autoantibody in acetylcholine receptor antibody-negative generalized acquired myasthenia gravisChan, KH; Mak, W; Cheung, RTF; Cheng, TS; Ho, SL200680
 
Myopia as a latent phenotype of a pleiotropic gene positively selected for facilitating neurocognitive development, and the effects of environmental factors in its expressionMak, W; Kwan, MWM; Cheng, TS; Chan, KH; Cheung, RTF; Ho, SL200668
 
An epidemiological study of motor neuron disease in Hong KongFong, 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, SL2005117
 
Clinical relevancy of severe initial hypertension in acute intracerebral haemorrhageCheng, TS; Cheung, RTF; Ho, SL200578
 
Clinical outcome between early and late settlement of high blood pressure in acute intracerebral haemorrhageCheng, TS; Cheung, RTF; Ho, SL200596
 
Cerebrospinal fluid to serum glucose ratio in non-hypoglycorrhachic neurological conditions.Mak, W; Cheng, TS; Chan, KH; Cheung, RTF; Ho, SL200574
 
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 arteriesMak, W; Cheng, TS; Chan, KH; Cheung, RTF; Ho, SL2005110
 
Wilson's disease with depression and parkinsonismChan, KH; Cheung, RTF; AuYeung, KM; Mak, W; Cheng, TS; Ho, SL2005134
 
Cerebellar degeneration and folate deficiency due to cough misture abuseAu, WY; Cheng, TS; Siu, TS; Yuen, KY2005105
 
Cerebrospinal fluid to serum glucose ratio in non-hypoglycorrhachic neurological conditionsMak, W; Cheng, TS; Chan, KH; Cheung, RTF; Ho, SL2005275
 
Bath-related headacheMak, W; Tsang, KL; Tsoi, TH; Au Yeung, KM; Chan, KH; Cheng, TS; Cheung, TFR; Ho, SL2005159
 
Natural course of patients presenting with acute myelitis.Chan, KH; Mak, W; Cheng, TS; Cheung, RTF; Ho, SL200480
 
Predictive factors for ischemic strokes complicating tuberculous meningitis.Chan, KH; Cheung, RTF; Mak, W; Fong, CY; Tsang, KL; Cheng, TS; Ho, SL200481
 
Re-exploring the cerebrospinal fluid (CSF) to serum glucose ratioMak, W; Cheng, TS; Fong, CYG; Tsang, KL; Chan, KH; Cheung, RTF; Ho, SL200470
 
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