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Showing results 210 to 229 of 472 < previous next >

Title	Author(s)	Issue Date	Views
Herpes zoster in juvenile-onset systemic lupus erythematosus: Incidence, clinical characteristics and risk factors Proceeding/Conference:Joint Annual Scientific Meeting, The Hong Kong Paediatric Society and Hong Kong Paediatric Nurses Association	Lee, PPW Lee, TL Ho, MHK Wong, WHS Lau, YL	2006	100
High frequency of spontaneous rupture of hepatoblastoma in children: a comparative analysis of Hepatoblastoma and Hepatocellular Carcinoma in a Singel Institution Proceeding/Conference:Annual Scientific Meeting of the Hong Kong Paediatric Society, HKPS 1999	Chiang, AKS Chan, GCF Chan, KL Tam, PKH Lau, YL	1999	87
Hong Kong needs a carrier screening programme for the thalassaemias Proceeding/Conference:Journal of Paediatrics and Child Health	Lau, YL Chan, LC Chan, ACL Ha, SY Waye, JS Chiu, DHK Yeung, CY	1997	84
Human herpesvirus 6 and human herpesvirus 7 infections in bone marrow transplant recipients Proceeding/Conference:International Herpesvirus Workshop	Chan, PHC Peiris, JSM Yuen, KY Liang, RHS Chen, FE Lau, YL Lo, S Cheung, CY Ng, MH	1997	129
Human monocyte derived dendritic cells infected by SARS associated coronavirus Proceeding/Conference:ICI-FOCIS 2004	Law, HKW Cheung, CY Ng, IHY Sia, SF Luk, W Nicholls, JM Peiris, JSM Lau, YL	2004	100
Hyper IgM syndrome presented as severe eosinophilia Proceeding/Conference:Journal of Paediatrics and Child Health	Leung, TNH So, LY Chow, SN Lau, YL	1997	115
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	105
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	94
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	53
Identification of 22q11.2 deletion in patients from adult congenital heart disease clinic: a missed burden in the transition care in Hong Kong Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2013	Chung, B Chow, P Liu, A Lee, P Chan, K Tang, M Lau, E Cheung, YF Chau, KT Lau, YL	2013	68
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	155
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	102
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	93
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	147
Identification of a CFTR founder mutations, c.3068T>G:p.I1023R, which causes protein trafficking defects in Chinese patients with cystic fibrosis Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Leung, KC Ying, D Mak, CCY Chen, XY Xu, W Yeung, KS Chu, WY Mok, TKG Chau, SKC McLuskey, J Ong, WPT Leong, HY Chan, YK Yang, W Chen, JH Li, AM Lau, YL Lee, SL Chung, BHY	2016	67
Identification of a novel homozygous missense mutation in ABR causing cerebellar hypoplasia with early lethality Proceeding/Conference:Asian Society for Pediatric Research & Faculty of Medicine Ramathibodi Hospital Joint Meeting, ASPR 2016	Leung, GKC Ying, D Shek, NWM Chu, WY Yeung, KS Tang, MHY Kan, SYA Chan, YK Ip, JKJ Yang, W Lau, YL Chung, BHY	2016	40
Identify a Novel Btk Splice Site Mutation in a Chinese Boy with XLA Proceeding/Conference:Hong Kong Journal of Paediatrics	Fang, P Jiang, LP Wang, JJ Wang, LJ Lau, YL Toshio, M Yang, XQ	2004	127
Identify a Novel CYBB Gene Mutation in a Chinese Boy with X-Linked Chronic Granulomer Disease and Its Carriers Proceeding/Conference:Hong Kong Journal of Paediatrics	Jiang, LP Mak, HS Wang, LJ Chan, KW Fang, P Luo, XJ Lau, YL Yang, XQ	2004	130
Identifying causal mutations for Primary Immunodeficiencies in Southeast Asian region using whole exome sequencing Proceeding/Conference:ICHG / ASHG 2011	Yang, J Yang, W Lee, PPW Zeng, S Zhang, L Sham, PC Lau, YL	2011	122
IFN-Gamma Microsatellite Region and Tuberculosis Proceeding/Conference:International Congress on Infectious Diseases	Cheng, FSK Tam, CM Lau, YL	2002	91

Showing results 210 to 229 of 472 < previous next >