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Title	Author(s)	Issue Date	Views
17p13.3 class I microduplication in a newborn with microcephaly, aortic stenosis and dysmorphic facial features Proceeding/Conference:Hong Kong Journal of Paediatrics (new series)	Ho, A Liu, A Lun, KS Tam, T Chan, K Lau, E Tang, M Tan, T Chung, B	2011	124
A fatal case of COQ7-associated primary coenzyme Q10 deficiency Journal:JIMD Reports	Kwong, AKY Chiu, ATG TSANG, MHY Lun, KS Rodenburg, RJT Smeitink, J Chung, BHY Fung, CW	2019
Abdominal submuscular implant of subcutaneous implantable cardioverter-defibrillator in a young child Journal:EP Europace	Kwok, SY Yam, N Lun, KS Chen, RHS Au, TWK Yung, TC	2018
Achieving biventricular circulation in patients with moderate hypoplastic right ventricle in pulmonary atresia intact ventricular septum after transcatheter pulmonary valve perforation Journal:Congenital Heart Disease	Chen, HSR Chau, AKT Chow, PC Yung, TC Cheung, YF Lun, KS	2018	13
Analysis of indications for surgical closure of subarterial ventricular septal defect without associated aortic cusp prolapse and aortic regurgitation Journal:American Journal of Cardiology	Lun, KS Li, H Leung, MP Chau, AKT Yung, TC Chiu, CSW Cheung, YF	2001	85
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	35
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	53
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
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	19
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	56
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	68
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	52
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	59
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	44
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	62
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	69
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	88
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	72

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