HKU Scholars Hub: Browsing DSpace

Browsing by Author rp01586

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 4 to 23 of 33 < previous next >

Title	Author(s)	Issue Date
A case of early-onset obesity, hypocortisolism, and skin pigmentation problem due to a novel homozygous mutation in the proopiomelanocortin (POMC) gene in an Indian boy Journal:Journal of Pediatric Endocrinology & Metabolism	Hung, CN Poon, DWT Lee, CY Law, CY Chan, AYW	2012
Cells that produce deleterious autoreactive antibodies are vulnerable to suicide Journal:Journal of Immunology	Niu, H Leung, DTM Chun, HM Law, ECY Tam, FCH Lim, PL	2008
Clinical whole-exome sequencing reveals a novel missense pathogenic variant of GNAO1 in a patient with infantile-onset epilepsy Journal:Clinica Chimica Acta	Law, CY Chang, T Cho, SY Yau, EK Ng, GS Fong, NC Lam, CW	2015
Difference in the Metabolome between Escherichia Coli Isolated from Patients with Pyelonephritis and Cholangitis Proceeding/Conference:Annual International Conference of the Metabolomics Society	To, KKW Lam, CW Lee, KC Yung, KY Law, CY Leung, KF Lau, KC Chan, SF	2013
Electronic chemical pathology consultation service and dried blood spot metabolic screening in hospital patients Journal:Journal of Clinical Pathology	Mak, CM Siu, WK Law, CY Wong, CK Lee, HK Yeung, S Sham, CO Tse, K Lee, HHC Chen, SPL Ching, CK Au, CK Poon, WT Lam, CW Kwong, NS Chan, AYW	2012
Fatal viral infection-associated encephalopathy in two Chinese boys: A genetically determined risk factor of thermolabile carnitine palmitoyltransferase II variants Journal:Journal of Human Genetics	Mak, CM Lam, CW Fong, NC Siu, WK Lee, HCH Siu, TS Lai, CK Law, CY Tong, SF Poon, WT Lam, DSY Ng, HL Yuen, YP Tam, S Que, TL Kwong, NS Chan, AYW	2011
Genetic diagnosis of severe myoclonic epilepsy of infancy (Dravet syndrome) with SCN1A mutations in the Hong Kong Chinese patients Journal:Hong Kong Medical Journal	Mak, CM Chan, KY Yau, EKC Chen, SPL Siu, WK Law, CY Lam, CW Chan, AYW	2011
Higher SARS-CoV-2 viral loads correlated with smaller thyroid volumes on ultrasound among male COVID-19 survivors Journal:Endocrine	Lui, DTW Fung, MMH Chiu, WHK Lee, CH Chow, WS Lee, ACH Tam, AR Pang, P Ho, TY Fong, CHY Loong, CHN Wong, WW Lee, CYY Law, CY To, KKW Lam, CW Tan, KCB Woo, YC Hung, IFN Lam, KSL Lang, BHH	2021
Identifying the disease gene for a new locus of congenital myasthenic syndrome Proceeding/Conference:Annual International Conference of the Metabolomics Society	Lam, CW Law, CY	2014
Lipid mediators of inflammation as novel plasma biomarkers to identify patients with bacteremia Journal:Journal of Infection	To, KKW Lee, KC Wong, SSY Lo, KC Lui, YM Akhee, SJ Wu, L Ke, Y Law, CY Sze, KH Lau, SKP Woo, PCY Lam, CW Yuen, KY	2015
Lipid metabolites as potential diagnostic and prognostic biomarkers for acute community acquired pneumonia Journal:Diagnostic Microbiology and Infectious Disease	To, KKW Lee, KC Wong, SSY Sze, KH Ke, Y Lui, YM Tang, BS Li, WS Lau, SKP Hung, FNI Law, CY Lam, CW Yuen, KY	2016
New lights in light's criteria Proceeding/Conference:RCPA Pathology Update Conference	Law, CY Lam, CW	2015
New lights in light's criteria Proceeding/Conference:Pathology	Law, CY Lam, CW	2015
NMR-based metabolomic urinalysis: A rapid screening test for urinary tract infection Journal:Clinica Chimica Acta	Lam, CW Law, CY To, KKW Cheung, SKK Lee, KC Sze, KH Leung, KF Yuen, KY	2014
NMR-based urinalysis for beta-ketothiolase deficiency Journal:Clinica Chimica Acta	Law, CY Lam, CW Ching, DCK Yau, KC Ho, TW Lai, CK Mak, CM	2015
NMR-based urinalysis for rapid diagnosis of inborn errors of metabolism Proceeding/Conference:RCPA Pathology Update Conference	Law, CY Lam, CW	2015
NMR-based urinalysis for rapid diagnosis of inborn errors of metabolism Proceeding/Conference:Pathology	Law, CY Lam, CW	2015
NMR-based urinalysis for rapid diagnosis of β-ureidopropionase deficiency in a patient with Dravet syndrome Journal:Clinica Chimica Acta	Lam, CW Law, CY Leung, KF Lai, CK Chen, SPL Chan, B Chan, KY Yuen, LYP Mak, CM Chan, AYW	2015
Non-invasive screening of HLA-DPA1 and HLA-DPB1 alleles for persistent hepatitis B virus infection: Susceptibility for vertical transmission and toward a personalized approach for vaccination and treatment Journal:Clinica Chimica Acta	Lau, KC Lam, CW Law, CY Lai, ST Tsang, TY Siu, CWK To, WK Leung, KF Mak, CM Poon, WT Chan, PKS Chan, YW	2011
Novel large deletion in AVPR2 gene causing copy number variation in a patient with X-linked nephrogenic diabetes insipidus Journal:Clinica Chimica Acta	Cho, SY Law, CY Ng, KL Lam, CW	2016

Showing results 4 to 23 of 33 < previous next >