Browsing by Author Fung, CW

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
Showing results 13 to 32 of 88 < previous   next >
TitleAuthor(s)Issue DateViews
 
2010
239
 
Children with mesial temporal sclerosis (MTS) in an epilepsy cohort - a different clinical spectrum?
Proceeding/Conference:50th Anniversary Symposium on Paediatric Neurology & Neuro-Rehabilitation
2005
18
 
2013
52
 
Clinical profile of 13 children with severe myoclonic epilepsy of infancy in Hong Kong
Proceeding/Conference:Asian & Oceanian Epilepsy Congress, AOEC 2010
2010
61
 
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
87
 
2012
170
 
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
26
 
2007
109
 
Copy number variation in Hong Kong patients with autism spectrum disorder
Proceeding/Conference:Hong Kong Journal of Paediatrics (New series)
2016
109
 
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
48
 
1999
80
 
1999
72
 
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
106
 
2012
33
Dravet syndrome - genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children
Proceeding/Conference:Developmental Medicine and Child Neurology
2012
115
Dravet Syndrome-Genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children
Proceeding/Conference:International Meeting for Autism Research
2012
104
 
2018
83
 
2019
93
 
2011
184
 
2014
124