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TypeTitleAuthor(s)YearViews
Identifying the Service Gaps in the Management of Severe Systemic Allergic Reaction/Anaphylaxis by Paediatrics Departments of the the Hospital AuthorityHo, MHK; Wong, LM; Ling, SC; Lee, KP; Cheng, WW; Hui, J; Lau, DCY; Ng, KL; Wong, D; Kwok, KL; Kwan, EYW2010119
 
An update on the epidemiology of childhood diabetes in Hong KongHuen, KF; Low, LCK; Cheung, PT; Wong, GWK; But, WM; Kwan, EYW; Lam, YY; Lee, CY; Wong, LM; Ng, KL; Cheng, AWF; Tong, CT; Wong, WHS2009289
 
Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuriaYuen, YP; Lam, CW; Lai, CK; Tong, SF; Li, PS; Tam, S; Kwan, EYW; Chan, SY; Tsang, WK; Chan, KY; Mak, WL; Cheng, CW; Chan, YW2006106
 
A family with osteoporosis pseudoglioma syndrome due to compound heterozygosity of two novel mutations in the LRP5 geneCheung, WMW; Jin, LY; Smith, DK; Cheung, PT; Kwan, EYW; Low, L; Kung, AWC2006123
 
Mutation analysis of the GLUT2 Gene in a Chinese patient with Fanconi-Bickel SyndromePoon, GWK; Kwan, EYW; Cheung, PT; Low, LCK200673
 
Aldosterone synthetase (corticosterone methyloxidase) deficiency type II in a Chinese boyCheung, PT; Low, LCK; Kwan, EYW200677
 
6-pyruvoyl-tetrahydropterin synthase deficiency: the clinical spectrum in 3 Chinese patientsFung, CW; Cheung, PT; Kwan, EYW; Poon, GWK; Low, LCK; Wong, VCN2006116
 
A family with osteoporosis-pseudoglioma syndrome (OPG) due to compound heterozygous mutation of the LRP5 geneJin, L; Lau, HL; Smith, DK; Lau, KS; Cheung, PT; Kwan, EYW; Low, LCK; Chan, VNY; Kung, AWC200595
 
Family with osteoporosis Pseudolioma Syndrome due to compound heterozygosity of two novel mutations of the LRP5 geneJin, L; Lau, HL; Smith, DK; Lau, KS; Cheung, PT; Kwan, EYW; Low, LCK; Chan, VNY; Kung, AWC200594
 
6-pyruvoyl-tetrahydropterin synthase deficiency, a potentially treatable cause of dystoniaFung, CW; Cheung, PT; Kwan, EYW; Poon, GWK; Low, LCK; Wong, VCN2005126
 
Prenatal Diagnosis and Prospective Management of Argininosuccinic Aciduria in the Prevention of Neonatal Hyperammonaemic ComaPoon, GWK; Lam, CW; Tang, MHY; Wong, KY; Kwan, EYW; Cheung, PT; Low, LCK2004108
 
Determinants of bone mineral density in Asian menGu, J; Lee, KK; Kwan, EYW; Lam, KF; Ho, AYY; Tam, S; Kung, AWC200494
 
Robust Under the Gust – 疾 風 勁 草'Chan, GCF; Kwan, EYW; Chiu, SY2004139
 
Robust Under the GustChan, GCF; Kwan, EYW; Chiu, SY2004149
 
Antenatal Diagnosis and Postnatal Management of Tetrahydrobiopterin-deficient Hyperphenyalaninemia in a Hong Kong Chinese InfantLee, PPW; Poon, GWK; Kwan, EYW; Wong, KY; Chan, KW; Lee, JSK; Tam, SCF; Lau, E; Tang, MHY; Gu, XF; Low, LCK; Cheung, PT2004114
 
A family with osteoporosis-pseudoglioma syndrome (OPG) due to compound heterozygous mutation of the LRO5 geneJin, L; Lau, HL; Smith, DK; Lau, KS; Cheung, PT; Kwan, EYW; Low, LCK; Kung, AWC2004103
 
A Pilot Study of the Use of Insulin Glargine in Combination with Short Acting Insulin Analogue in Adolescents with Type I Diabetes Mellitus in Hong KongAu, RWM; Kwan, EYW; Yeung, LPK; Cheung, PT; Low, LCK200477
 
Positive Corrleation of Selective IGF-I Genotypes with Idiopathic Short Stature in Chinese ChildrenMan, E; Tan, KCB; Chan, KW; Yeung, LPK; Kwan, EYW; Wong, WHS; Low, LCK; Cheung, PT200480
 
Mutation Analysis of the GLUT2 Gene in a Chinese Patient with Fanconi-Bickel SyndromePoon, GWK; Cheung, PT; Chen, RT; Kwan, EYW; Low, LCK200481
 
Measles-mumps-rubella Vaccination and Egg AllergyChow, WC; Kwan, EYW; Lau, YL2003101
 
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