Results 1 to 20 of 54
Page 1 of 3  Next >
TypeTitleAuthor(s)YearViews
Folinic acid responsive epilepsy in Ohtahara Syndrome caused by STXBP1 mutation
Journal:
Pediatric Neurology
Tso, WYW; Kwong, AK; Fung, CW; Wong, VCN201431
 
Lathosterolosis: A Disorder Of Cholesterol Biosynthesis Resembling Smith-lemli-opitz Syndrome
Journal:
Journal Of Inherited Metabolic Disease
Ho, CCA; Fung, CW; Siu, TS; Ma, OCK; Lam, CW; Tam, S; Wong, VCN201437
 
Clinical And Genetic Evaluation Of 23 Children With Infantile Onset Epileptic Encephalopathy (iee)
Proceedings/Conference:
The 3rd Hong Kong Neurological Congress Cum 26th Annual Scientific Meeting Of The Hong Kong Neurological Society. 2-3 November, 2013
Ho, CCA; Kwong, KY; Fung, CW; Wong, VCN201320
 
Arginase deficiency with new phenotype and a novel mutation: Contemporary Summary
Journal:
Pediatric Neurology
Tsang, JPK; Poon, WL; Luk, HM; Fung, CW; Ching, CK; Mak, CM; Lam, CW; Siu, TS; Tam, S; Wong, VCN201274
 
Dravet Syndrome-Genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children.
Proceedings/Conference:
International Meeting for Autism Research, Toronto, Ontario, Canada, 17-19 May
Wong, VCN; Kwong, KY; Fung, CW201299
 
COG5-CDG with a Mild Neurohepatic Presentation
Journal:
JIMD Reports
Publisher:
SSIEM and Springer-verlag Berlin Heidelberg.
Fung, CW; Matthijs, G; Sturiale, L; garozzo, D; Wong, KY; Wong, RMS; Wong, VCN; Jaeken, J2012118
 
Dravet syndeome: genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children
Proceedings/Conference:
Hong Kong Medical Journal
Publisher:
Hong Kong Academy of Medicine Press. The Journal's web site is located at http://www.hkmj.org.hk
Wong, VCN; Kwong, A; Fung, CW201251
 
Dravet syndrome - genetic analysis of SCN1A and PCDH19 mutations for 17 Chinese children
Proceedings/Conference:
Developmental Medicine and Child Neurology
Publisher:
Mac Keith Press. The Journal's web site is located at http://www.mackeith.co.uk/journal.html
Wong, V; Kwong, A; Fung, CW2012118
 
Paroxysmal non-epileptic movements in childhood
Journal:
HK Journal of Paediatrics (new series)
Fung, CW; Wong, VCN2012104
 
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong
Proceedings/Conference:
Developmental Medicine and Child Neurology
Publisher:
Mac Keith Press. The Journal's web site is located at http://www.mackeith.co.uk/journal.html
Fung, CW; Smeitenk, J; Rodenburg, R; Siu, S; Ma, O; Poon, G; Tam, S; Wong, V2012135
 
Identification of SCN1A and PCDH19 mutations in Chinese children with Dravet syndrome
Journal:
PLoS ONE
Publisher:
Public Library of Science. The Journal's web site is located at http://www.plosone.org/home.action
Kwong, AKY; Fung, CW; Chan, SY; Wong, VCN2012158
 
Expanding phenotype and clinical analysis of tyrosine hydroxylase deficiency
Journal:
Journal of Child Neurology
Publisher:
Sage Publications, Inc.. The Journal's web site is located at http://jcn.sagepub.com
Yeung, WL; Wong, VCN; Chan, KY; Hui, J; Fung, CW; Yau, E; Ko, CH; Lam, CW; Mak, CM; Siu, S; Low, L2011297
 
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong
Proceedings/Conference:
Hospital Authority Convention 2011
Wong, VCN; Fung, CW201177
 
Clinical profile of 13 children with severe myoclonic epilepsy of infancy in Hong Kong
Proceedings/Conference:
Asian & Oceanian Epilepsy Congress
Fung, CW; Wong, VCN201078
 
Kbg syndrome: Clinical features and specific dental findings
Journal:
Pediatric Dentistry
Publisher:
American Academy of Pediatric Dentistry. The Journal's web site is located at http://www.aapd.org/publications/peddent/
Almandey, HA; Anthonappa, RP; King, NM; Fung, CW2010183
 
Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese
Journal:
Molecular Genetics and Metabolism
Publisher:
Academic Press. The Journal's web site is located at http://www.elsevier.com/locate/ymgme
Mak, CM; Lam, CW; Siu, TS; Chan, KY; Siu, WK; Yeung, WL; Hui, J; Wong, VCN; Low, LCK; Ko, CH; Fung, CW; Chen, SP; Yuen, YP; Lee, HC; Yau, E; Chan, B; Tong, SF; Tam, S; Chan, YW2010306
 
Anti-NMDA receptor encephalitis with atypical brain changes on MRI
Journal:
Pediatric Neurology
Publisher:
Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/pedneu
Chan, SHS; Wong, VCN; Fung, CW; Dale, RC; Vincent, A2010171
 
A study of cerebrospinal fluid neurotransmitters assay in children with undiagnosed neurological diseases in Hong Kong
Proceedings/Conference:
Proceedings of the International Symposium on Epilepsy in Neurometabolic Diseases
Fung, CW; Poon, G; Kwok, A; Cheung, PT; Low, L; Blau, N; Siu, S; Mak, C; Tam, S; Wong, V2010178
 
Spectrum of mitochondrial diseases in a tertiary referral centre in Hong Kong
Proceedings/Conference:
International Symposium on Epilepsy in Neurometabolic Diseases, ISENMD 2010
Publisher:
ISENMD.
Fung, CW; Poon, G; Kwok, A; Cheung, PT; Low, L; Mak, C; Tam, S; Siu, S; Wong, V2010200
 
Infantile Convulsion Choreoathetosis Syndrome in a Hong Kong Chinese Family
Proceedings/Conference:
ASHG 2009 Annual Meeting, Hawaii, Honolulu, 20-24 October 2009
Fung, CW; Chung, BHY; Ng, P; Zhao, M; Yang, W; Wong, VCN2009150
 
Page 1 of 3  Next >
Export Records
Step 1: Select content and export format
  • Citation only
Step 2: Select export method
  • Download