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Browsing "Paediatrics & Adolescent Medicine: Conference papers" by Author wong, ky
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Showing results 1 to 17 of 17
Title
Author(s)
Issue Date
Views
Antenatal diagnosis and postnatal management of tetrahydrobiopterin-deficient hyperphenyalaninemia in a Hong Kong Chinese Infant
Proceeding/Conference:
Hong Kong Journal of Paediatrics (New Series)
Lee, PPW
Poon, GWK
Kwan, EYW
Wong, KY
Chan, KW
Lee, JSK
Tam, SCF
Lau, E
Tang, MHY
Gu, XF
Low, LCK
Cheung, PT
2004
130
Changes in epidemioloyg of extremely low birth weight infants (ELBW): implications for resource use
Proceeding/Conference:
Asian Pacific Congress of Pediatrics
Ting, JY
Wong, MSC
Wong, RMS
Wong, KY
2009
122
Coinfection of multiple strains of Epstein-Barr Virus in normal immunocompetent individuals
Proceeding/Conference:
Blood
Chiang, AKS
Wong, KY
Chan, GCF
Ha, SY
Lau, YL
Srivastava, G
1999
Delection of ROMK Gene in a pair of siblings with antenatal bartter Syndrome
Proceeding/Conference:
Hong Kong Journal of Paediatrics (New Series)
Lee, PPW
Wong, KY
Chan, KW
Chim, S
Low, LCK
Cheung, PT
2004
Identification of epigenetic alterations in imprinting growth disorders
Proceeding/Conference:
HKU Department of Paediatrics & Adolescent Medicine Golden Jubilee Scientific Meeting
Wong, WL
Chu, WY
Yeung, KS
Mak, CCY
Wong, KY
Li, RHW
Tang, MHY
Chung, BHY
2014
Neonatal and early neuro-developmental outcomes of extreme-low-birth-weight (ELBW) infants from single and multiple pregnancies
Proceeding/Conference:
The 7th Guangdong-Hong Kong and 1st Hong Kong-Guangdong-Shanghai-Chongqing Paediatric Exchange Meeting
Ting, JY
Wong, KY
2008
24
Neonatal and early neurodevelopmental outcomes of small-for-gestational age (SGA) extreme-low-birth-weight (ELBW) infants
Proceeding/Conference:
Guangdong-Hong Kong and 1st Guangdong-Hong Kong-Chongqing-Shanghai Paediatric Exchange Meeting
Ting, JY
Wong, KY
2008
101
Partial deletion of the gene encoding inwardly-rectifying potassium channel (ROM-K) causing antenatal bartter syndrome in a child born to consanguinous parents
Proceeding/Conference:
Annual Meeting of the Endocrine Society, ENDO 2000
Cheung, PT
Wong, KY
Chan, KW
Lam, BCC
Tang, MHY
Low, LCK
2000
Prenatal diagnosis and prospective management of argininosuccinic aciduria in the prevention of neonatal hyperammonaemic coma
Proceeding/Conference:
Hong Kong Journal of Paediatrics
Poon, GWK
Lam, CW
Tang, MHY
Wong, KY
Kwan, EYW
Cheung, PT
Low, LCK
2004
170
A rare cause of hepatosplenomegaly - transaldolase deficiency
Proceeding/Conference:
Journal of Inherited Metabolic Disease
Fung, CW
Siu, S
Mak, CM
Poon, GWK
Wong, KY
Cheung, PT
Low, LCK
Tam, S
Wong, VCN
2007
156
A rare cause of hepatosplenomegaly transaldolase deficiency
Proceeding/Conference:
Joint Annual Scientific Meeting for Paediatricians & Paediatric Nurses
Fung, CW
Siu, S
Mak, CM
Poon, GWK
Wong, KY
Cheung, PT
Low, LCK
Tam, S
Wong, VCN
2007
Reversible Myocardial Damage in a Premature Infant with Carnitine-Acylcarnitine Translocase Deficiency
Proceeding/Conference:
Hong Kong Journal of Paediatrics
Poon, GWK
Mak, CM
Wong, RMS
Wong, KY
Yung, TC
Tam, S
Siu, STS
Lee, JSK
Low, LCK
2004
Selective abortion for congenital disorders: Discordance in attitudes among professionals and laymen
Proceeding/Conference:
HKPS-HKPNA 2004 Joint Annual Scientific Meeting
Chan, GCF
Ng, MW
Lam, WWT
Fong, DYT
Lau, TTH
Wong, KY
Fielding, R
2004
169
Treatment of Paediatric Extracranial Germ Cell Tumour
Proceeding/Conference:
The 14th Asia Pacific Cancer Conference & 4th Hong Kong International Cancer Congress
Lee, ACW
Ha, SY
Wong, KY
Cheng, MY
Fung, AWC
Tsui, KY
Chan, GCF
Lau, YL
1997
82
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
Chung, BHY
Fung, CW
Li, YH
Wong, KY
Chan, GCF
Wong, VCN
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
Chung, BHY
Fung, CW
Li, YH
Wong, KY
Chan, GCF
Wong, VCN
2005
79
Two novel mutations of SMPD1 gene from a Chinese family with niemann pick disease type A (NPD-A)
Proceeding/Conference:
Hong Kong Medical Genetics Conference
Chung, BHY
Fung, CW
Li, S
Wong, KY
Chan, GCF
Wong, VCN
2005
97