Browsing by Author Fung, CW

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TitleAuthor(s)Issue DateViews
 
Clinical profile of 13 children with severe myoclonic epilepsy of infancy in Hong Kong
Proceeding/Conference:Asian & Oceanian Epilepsy Congress, AOEC 2010
2010
45
 
The clinical utility of radiologic screening in asymptomatic neurofibromatosis-1 (NF-1)
Proceeding/Conference:Annual Meeting of the Society for Pediatric Radiology, SPR 2002
2002
59
 
2012
 
Comprehensive genetic evaluation in paediatric-onset mitochondrial diseases
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
 
2007
70
 
Copy number variation in Hong Kong patients with autism spectrum disorder
Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)
2016
63
 
COQ10 deficiency due to biallelic COQ4 mutations – An early onset mitochondrial disorder common in southern Chinese due to a founder mutation
Proceeding/Conference:2nd Joint Annual Research & Scientific Meeting 2018 of the Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association and Hong Kong College of Paediatric Nursing
2018
 
2020
 
1999
44
 
1999
44
 
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
 
2012
44
Dravet syndrome - genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children
Proceeding/Conference:Developmental Medicine and Child Neurology
2012
120
Dravet Syndrome-Genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children
Proceeding/Conference:International Meeting for Autism Research
2012
98
 
2018
6
 
2019
28
 
2011
140
 
2014
 
2017
19
 
2008
80