Browsing by Author Fung, CW

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TitleAuthor(s)Issue DateViews
 
A rare cause of hepatosplenomegaly transaldolase deficiency
Proceeding/Conference:Joint Annual Scientific Meeting for Paediatricians & Paediatric Nurses
2007
131
 
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
109
 
Review of 17 children with cyclic vomiting syndrome
Proceeding/Conference:Chinese Paediatric Forum
1996
88
 
2015
196
 
Revisiting ischaemia and reperfusion injury as a possible cause for necrotising enterocolitis
Proceeding/Conference:Annual Scientific Meeting of the Australasian Association of Paediatric Surgeons
2001
120
 
2015
75
 
2004
141
 
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong
Proceeding/Conference:Hospital Authority Convention, HAC 2011
2011
76
 
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
121
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong
Proceeding/Conference:Developmental Medicine and Child Neurology
2012
195
 
2005
158
 
A study of cerebrospinal fluid neurotransmitters assay in children with undiagnosed neurological diseases in Hong Kong
Proceeding/Conference:International Symposium on Epilepsy in Neurometabolic Diseases, ISENMD 2010 Proceedings
2010
166
 
2009
174
 
2019
18
 
2020
35
 
The KLHL40C.1516A>C is a Chinese-specific founder mutation in causing nemaline myopathy 8
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
 
2005
179
 
Two novel mutations of SMPD1 gene from a Chinese family with Niemann Pick Disease type A (NPD-A)
Proceeding/Conference:HKPS-HKPNA 2006 Joint Annual Scientific Meeting
2006
100
 
Two novel mutations of SMPD1 gene from a Chinese family with Niemann Pick Disease Type A (NPD-A)
Proceeding/Conference:50th Anniversary Symposium on Paediatric Neurology & Neuro-Rehabilitation
2005
77
 
2005
97