Skip navigation
HKU Login
Guest Login
Home
Publications
Researchers
Staff
Research Postgraduates
Organizations
Grants
Datasets
Deposit Data
HKUL Research Data Management
Theses
Patents
Community Service
Browsing by Author Lun, KS
Jump to:
0-9
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
中
or enter first few letters:
Showing results 6 to 25 of 54
< previous
next >
Title
Author(s)
Issue Date
Views
Brain natriuretic peptide as a biomarker of systemic right ventricular function in patients with transposition of great arteries after atrial switch operation
Journal:
International Journal of Cardiology
Chow, Pc
Cheung, EWy
Chong, Cy
Lun, Ks
Yung, Tc
Wong, Kt
Chau, AKt
Cheung, Yf
2008
Cardiovascular symptoms and signs in evaluating cardiac murmurs in children
Journal:
Pediatrics International
Koo, S
Yung, TC
Lun, KS
Chau, AKT
Cheung, YF
2008
63
Clinical and genetic profile of catecholaminergic polymorphic ventricular tachycardia in Hong Kong Chinese children
Journal:
Hong Kong Medical Journal
Yu, TC
Yung, TC
Lun, KS
Chung, BHY
Liu, APY
2016
118
Clinical and Genetic Profile of Congenital Long QT Syndrome in Hong Kong - 18-year Experience in Paediatrics
Proceeding/Conference:
26th Annual Scientific Congress of Hong Kong College of Cardiology, 2018
Kwok, SY
Liu, APY
Chan, CYY
Lun, KS
Fung, LF
MAK, CCY
Chung, BHY
Yung, TC
2018
37
Clinical and genetic profile of congenital long QT syndrome in Hong Kong: a 20-year experience in paediatrics
Journal:
Hong Kong Medical Journal
Kwok, SY
Liu, APY
Chan, CYY
Lun, KS
Fung, LF
Mak, CCY
Chung, BHY
Yung, TC
2018
94
Differential impact of right ventricular pacing on three-dimensional global left ventricular dyssynchrony in children and young adults with congenital and acquired heart block
Proceeding/Conference:
World Congress of Paediatric Cardiology & Cardiac Surgery, WCPCCS 2009
Hong, W
Yung, TC
Lun, KS
Cheung, YF
2009
102
Differential impact of right ventricular pacing on three-dimensional global left ventricular dyssynchrony in children and young adults with congenital and acquired heart block
Proceeding/Conference:
Congress of Asian Society for Pediatric Research, ASPR 2009
Hong, W
Weng, D
Weng, D
Lun, KS
Cheung, YF
2009
Doppler tissue imaging analysis of ventricular function after surgical and transcatheter closure of atrial septal defect
Journal:
American Journal of Cardiology
Cheung, YF
Lun, KS
Chau, AKT
2004
83
Emerging roles of left ventricular assist device therapy as bridge to transplant in an Asian city with scarce heart donor
Journal:
Journal of Thoracic Disease
Wong, KL
Ho, KLC
Lee, OJ
Lun, KS
Bhatia, I
Tam, WYE
Fan, YYK
Au, TWK
2021
7
Evaluating High‐Confidence Genes in Conotruncal Cardiac Defects by Gene Burden Analyses
Journal:
Journal of the American Heart Association Cardiovascular and Cerebrovascular Disease
Chui, MMC
Mak, CCY
Yu, MHC
Wong, SYY
Lun, KS
Yung, TC
Kwong, AKY
Chow, PC
Chung, BHY
21-Feb-2023
Evolution of the management approach for pulmonary atresia with intact ventricular septum
Journal:
Heart
Mi, YP
Chau, AKT
Chiu, CSW
Yung, TC
Lun, KS
Cheung, YF
2005
130
Experience of pediatric heart transplantation in Hong Kong
Proceeding/Conference:
European Heart Journal Supplements
Lun, KS
Fan, K
Yung, TC
Wong, KT
Cheung, YF
Chau, AKT
Cheng, LC
2010
66
Fate of the unligated vertical vein after repair of supracardiac anomalous pulmonary venous connection
Journal:
Journal of Paediatrics and Child Health
Cheung, YF
Lun, KS
Chau, AKT
Chiu, CSW
2005
55
Identification of 21 novel and 3 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes
Proceeding/Conference:
Annual Congress of the Asian Society for Pediatric Research, ASPR 2006
Chung, BHY
Lam, STS
Tong, TMF
Li, YH
Lun, KS
Chan, HC
Or, SF
Lau, YL
2006
114
Identification of 21 novel and 3 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes
Proceeding/Conference:
HUGO / HUGO-AP 2006
Lun, KS
Lam, STS
Tong, TMF
Chung, BHY
Li, YH
Chan, HC
Or, SF
Lau, YL
2006
101
Identification of 22q11.2 deletion in patients from adult congenital heart disease clinic - a missed burden in the transition care
Proceeding/Conference:
European Journal of Human Genetics
Chung, B
Chow, P
Liu, A
Lee, P
Wong, V
Chan, K
Tang, M
Lun, KS
Lau, ETK
Cheung, YF
Chau, KT
Lau, YL
2013
69
Identification of 25 novel and 2 known FBN1 mutations in 66 unrelated Chinese probands with Marfan syndrome or Marfan-like phenotypes
Proceeding/Conference:
HKPS-HKPNA 2006 Joint Annual Scientific Meeting
Chung, BHY
Lam, STS
Tong, TMF
Li, YH
Lun, KS
Chan, HC
Or, SF
Lau, YL
2006
Identification of 7 novel TGFBR2 (Transforming Growth Factor-Beta Receptor 2) mutations in Chinese with Marfan syndrome (MFS) and related phenotypes using denaturing high performance liquid chromatography (DHPLC)
Proceeding/Conference:
International Congress of Pediatrics, IPA 2007
Chung, BHY
Li, YH
Lam, STS
Yang, W
Lun, KS
Lau, YL
2007
Identification of 7 novel TGFBR2 mutations in Chinese with marfan syndrome (MFS) and related phenotypes using DHPLC
Proceeding/Conference:
Congress of Asian Society for Pediatric Research, ASPR 2007
Chung, BHY
Li, YH
Lam, STS
Yang, W
Lun, KS
Lau, YL
2007
106
Identification of 7 novel transforming growth factor β receptor 2 mutations in Chinese patients with marfan syndrome
Proceeding/Conference:
Pediatrics
Chung, BHY
Li, YH
Lam, STS
Yang, W
Lun, KS
Lau, YL
2008
