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
134
 
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
104
 
Review of 17 children with cyclic vomiting syndrome
Proceeding/Conference:Chinese Paediatric Forum
1996
82
 
2015
164
 
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
112
 
2015
74
 
2004
133
 
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong
Proceeding/Conference:Hospital Authority Convention, HAC 2011
2011
74
 
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
127
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong
Proceeding/Conference:Developmental Medicine and Child Neurology
2012
171
 
2005
141
 
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
160
 
2009
177
 
2019
15
 
2020
28
 
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
22
 
2005
159
 
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
95
 
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
72
 
2005
87