Browsing "Paediatrics & Adolescent Medicine: Conference papers" by Author fung, cw

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TitleAuthor(s)Issue DateViews
 
2012
23
Dravet syndrome - genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children
Proceeding/Conference:Developmental Medicine and Child Neurology
2012
164
Dravet Syndrome-Genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children
Proceeding/Conference:International Meeting for Autism Research
2012
144
 
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
34
 
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
33
 
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
18
 
Infantile Convulsion Choreoathetosis Syndrome in a Hong Kong Chinese Family
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009
2009
168
 
Infantile convulsion choreoathetosis syndrome in a Hong Kong Chinese Family
Proceeding/Conference:ACGA-HKSMG 2008 International Conference
2008
124
 
Infantile convulsion choreoathetosis syndrome in a Hong Kong Chinese family
Proceeding/Conference:Asian & Oceanian Epilepsy Congress, AOEC 2008
2008
128
 
Mutation of the LDHD gene in a Chinese girl with global developmental delay, transient hepatomegaly, hyperlactataemia and mitochondrial complex IV deficiency
Proceeding/Conference:The 16th Conference of Asian Society for Mitochondrial Research and Medicine (ASMRM) & The 19th Conference of Japanese Society of Mitochondrial Research and Medicine (J-mit), 2019
2019
23
 
Neuromuscular involvement in children with mitochondrial disease: A single centre experience
Proceeding/Conference:14th Asian and Oceanian Congress of Child Neurology
2017
26
2007
148
 
A rare cause of hepatosplenomegaly - transaldolase deficiency
Proceeding/Conference:Annual Symposium of Society for the Study of Inborn Errors of Metabolism, SSIEM 2007
2007
120
A rare cause of hepatosplenomegaly - transaldolase deficiency
Proceeding/Conference:Journal of Inherited Metabolic Disease
2007
137
 
A rare cause of hepatosplenomegaly transaldolase deficiency
Proceeding/Conference:Joint Annual Scientific Meeting for Paediatricians & Paediatric Nurses
2007
107
 
A rare presentation of 6-pyruvoyl tetrahydropterin synthase (PTPS) deficiency - Dopa Responsive Dystronia (DRD)
Proceeding/Conference:Joint Annual Scientific Meeting for Paediatricians & Paediatric Nurses
2007
98
 
Review of 17 children with cyclic vomiting syndrome
Proceeding/Conference:Chinese Paediatric Forum
1996
82
 
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong
Proceeding/Conference:International Symposium on Epilepsy in Neurometabolic Diseases, ISENMD 2010 Proceedings
2010
98
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong
Proceeding/Conference:Developmental Medicine and Child Neurology
2012
168
 
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong
Proceeding/Conference:Hospital Authority Convention, HAC 2011
2011
72