Search Results - "Fong, Gardian C.Y"

An epidemiological study of epilepsy in Hong Kong SAR, China by Fong, Gardian C.Y, Kwan, Patrick, Hui, Andrew C.F, Lui, Colin H.T, Fong, Jason K.Y, Wong, Virginia

“…Summary Background Several specialist clinic-based epidemiology studies suggested low prevalence in Hong Kong Special Administrative Region (HKSAR) of China…”
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Knowledge of stroke in Hong Kong Chinese by Cheung, R T, Li, L S, Mak, W, Tsang, K L, Lauder, I J, Chan, K H, Fong, G C

“…A random telephone survey on knowledge of stroke was conducted in 1, 238 Hong Kong Chinese. Most respondents realized that effective treatment was available,…”
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A Genetic Locus for Adolescent Idiopathic Scoliosis Linked to Chromosome 19p13.3 by Chan, Vivian, Fong, Gardian C.Y., Luk, Keith D.K., Yip, Ben, Lee, Miu-Kuen, Wong, Man-Sim, Lu, David D.S., Chan, Tai-Kwong

“…Adolescent idiopathic scoliosis (AIS) is one of the most common orthopedic disorders, affecting up to 4% of schoolchildren worldwide. We studied seven…”
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An update of the Hong Kong Epilepsy Guideline: consensus statement on the use of antiepileptic drugs in Hong Kong by Fong, J Ky, Chan, E Ly, Leung, H, Chan, I, Chang, R Sk, Fong, G Cy, Fung, E Lw, Lui, C Ht, Fung, B Bh, Poon, T L, Siu, D, Wong, H T, Yeung, E, Yung, A Wy, Zhu, C Xl

“…New information about antiepileptic drugs has arisen since the publication of the Hong Kong Epilepsy Guideline in 2009. This article set out to fill the…”
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Burkitt lymphoma presenting as posterior reversible encephalopathy syndrome secondary to hypercalcaemia by Ma, Edmond S. K., Chiu, Edmond K. W., Fong, Gardian C. Y., Li, Fu‐Keung, Wong, Chris L. P.

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Clinical phenotypes of a large Chinese multigenerational kindred with autosomal dominant familial ALS due to Ile149Thr SOD1 gene mutation by Fong, Gardian C. Y., Kwok, Ken H. H., Song, Y. Q., Cheng, T. S., Ho, Philip W. L., Chu, Andrew C. Y., Kung, Michelle H. W., Chan, K. H., Mak, Windsor, Cheung, Raymond T. F., Ramsden, David B., Ho, S. L.

“…About 10% of amyotrophic lateral sclerosis (ALS) cases are familial. We identified a five-generation Chinese family with autosomal dominant familial ALS…”
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An ex-intravenous drug addict with confusion and apathy by Chan, Koon H, Cheung, Raymond T F, Fong, Gardian C Y, Ho, Shu L

“…Wernicke's encephalopathy is an acute neurological disease, which is the result of thiamine deficiency. Cases in people who are not alcoholics are increasingly…”
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