Browsing by Author Fung, CW

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TitleAuthor(s)Issue DateViews
 
2020
14
 
1999
129
 
1999
100
 
A diagrammatic approach to search for minimum sampling frequency and quantization resolution for digital control of power converters
Proceeding/Conference:PESC Record - IEEE Annual Power Electronics Specialists Conference
2007
184
 
2012
37
Dravet syndrome - genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children
Proceeding/Conference:Developmental Medicine and Child Neurology
2012
184
Dravet Syndrome-Genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children
Proceeding/Conference:International Meeting for Autism Research
2012
173
 
Effect of olive oil phenol hydroxytyrosol (HT) in patient cell model with mitochondrial complex deficiency
Proceeding/Conference:Joint Annual Scientific Meeting 2020 (Virtual Meeting) of The Hong Kong Paediatric Society (HKPS), Hong Kong College of Paediatricians (HKCPaed), Hong Kong Paediatric Nurses Association (HKPNA) and Hong Kong College of Paediatric Nursing (HKCPN)
2020
17
 
2018
89
 
2019
96
 
2021
24
 
2011
243
 
2014
133
 
2017
63
 
2008
179
 
High diagnostic yield by whole exome sequencing in a cohort of patients with movement disorders and/or progressive spasticity – possible targeted treatment implications and a way to precison medicine
Proceeding/Conference:Joint Annual Scientific Meeting 2019 of The Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association, & Hong Kong College of Paediatric Nursing
2019
24
 
2012
90
 
Improving genetic diagnosis by whole exome sequencing in rare hereditary peripheral neuropathies
Proceeding/Conference:Hong Kong College of Paediatricians 4th Annual Scientific Meeting cum 5th HK-Guangdong-Shanghai-Chongquing Paediatric Exchange Meeting
2016
20
 
Infantile convulsion choreoathetosis syndrome in a Hong Kong Chinese family
Proceeding/Conference:Asian & Oceanian Epilepsy Congress, AOEC 2008
2008
165
 
Infantile Convulsion Choreoathetosis Syndrome in a Hong Kong Chinese Family
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009
2009
192