Results 1 to 20 of 101
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TypeTitleAuthor(s)YearViews
The clinical significance of aldosterone synthase deficiency: report of a novel mutation in the CYP11B2 gene.
Journal:
BMC Endocrine Disorder.
Hui, YLE; Yeung, MC; Cheung, PT; Kwan, EYW; Tan, KCB; Lam, KSL; Chan, AOK201421
 
Identifying the Service Gaps in the Management of Severe Systemic Allergic Reaction/Anaphylaxis by Paediatrics Departments of the the Hospital Authority
Journal:
Hong Kong Journal of Paediatrics (new series)
Ho, MHK; Wong, LM; Ling, SC; Lee, KP; Cheng, WW; Hui, J; Lau, DCY; Ng, KL; Wong, D; Kwok, KL; Kwan, EYW2010173
 
An update on the epidemiology of childhood diabetes in Hong Kong
Journal:
Hong Kong Journal of Paediatrics
Publisher:
Medcom Limited. The Journal's web site is located at http://www.hkjpaed.org/index.asp
Huen, KF; Low, LCK; Cheung, PT; Wong, GWK; But, WM; Kwan, EYW; Lam, YY; Lee, CY; Wong, LM; Ng, KL; Cheng, AWF; Tong, CT; Wong, WHS2009396
 
Mutation analysis of the GLUT2 Gene in a Chinese patient with Fanconi-Bickel Syndrome
Proceedings/Conference:
4th Biennial Scientific Meeting of the Asia Pacific PaediatricEndocrine Society, Pattaya, Thailand, 1-4 November
Poon, GWK; Kwan, EYW; Cheung, PT; Low, LCK2006111
 
Aldosterone synthetase (corticosterone methyloxidase) deficiency type II in a Chinese boy
Proceedings/Conference:
4th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society, Pattaya, Thailand, 1 - 4 November
Cheung, PT; Low, LCK; Kwan, EYW2006101
 
6-pyruvoyl-tetrahydropterin synthase deficiency: the clinical spectrum in 3 Chinese patients
Proceedings/Conference:
10th International Child Neurology Congress, Montreal, Canada, 11-16 June, 2006 (Abstract published in Neuropediatrics)
Fung, CW; Cheung, PT; Kwan, EYW; Poon, GWK; Low, LCK; Wong, VCN2006168
 
Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria
Journal:
Kidney International
Publisher:
Nature Publishing Group. The Journal's web site is located at http://www.nature.com/ki/index.html
Yuen, YP; Lam, CW; Lai, CK; Tong, SF; Li, PS; Tam, S; Kwan, EYW; Chan, SY; Tsang, WK; Chan, KY; Mak, WL; Cheng, CW; Chan, YW2006186
 
A family with osteoporosis pseudoglioma syndrome due to compound heterozygosity of two novel mutations in the LRP5 gene
Journal:
Bone
Publisher:
Elsevier Inc. The Journal's web site is located at http://www.elsevier.com/locate/bone
Cheung, WMW; Jin, LY; Smith, DK; Cheung, PT; Kwan, EYW; Low, L; Kung, AWC2006193
 
A family with osteoporosis-pseudoglioma syndrome (OPG) due to compound heterozygous mutation of the LRP5 gene
Proceedings/Conference:
HKU 10th Medical Research Conference
Jin, L; Lau, HL; Smith, DK; Lau, KS; Cheung, PT; Kwan, EYW; Low, LCK; Chan, VNY; Kung, AWC2005146
 
Family with osteoporosis Pseudolioma Syndrome due to compound heterozygosity of two novel mutations of the LRP5 gene
Proceedings/Conference:
6th Regional Osteoporosis Conference, 21-22 May 2005, Hong Kong
Jin, L; Lau, HL; Smith, DK; Lau, KS; Cheung, PT; Kwan, EYW; Low, LCK; Chan, VNY; Kung, AWC2005138
 
6-pyruvoyl-tetrahydropterin synthase deficiency, a potentially treatable cause of dystoniaFung, CW; Cheung, PT; Kwan, EYW; Poon, GWK; Low, LCK; Wong, VCN2005185
 
Prenatal Diagnosis and Prospective Management of Argininosuccinic Aciduria in the Prevention of Neonatal Hyperammonaemic Coma
Proceedings/Conference:
Ruby Jubilee Scientific Meeting, HK, 24-26 September 2004 (Abstract in Hong Kong Journal of Paediatrics (new series)
Publisher:
Medcom Limited.
Poon, GWK; Lam, CW; Tang, MHY; Wong, KY; Kwan, EYW; Cheung, PT; Low, LCK2004159
 
Determinants of bone mineral density in Asian men
Proceedings/Conference:
26th Annual Meeting of the American Society for Bone & Mineral Research, October 1-5, 2004, Seattle, USA. Journal of Bone and Mineral Research
Gu, J; Lee, KK; Kwan, EYW; Lam, KF; Ho, AYY; Tam, S; Kung, AWC2004138
 
Robust Under the Gust – 疾 風 勁 草'Chan, GCF; Kwan, EYW; Chiu, SY2004167
 
Robust Under the GustChan, GCF; Kwan, EYW; Chiu, SY2004181
 
Antenatal Diagnosis and Postnatal Management of Tetrahydrobiopterin-deficient Hyperphenyalaninemia in a Hong Kong Chinese Infant
Proceedings/Conference:
Ruby Jubilee Scientific Meeting, HK, 24-26 September 2004 (Abstract in Hong Kong Journal of Paediatrics (new series)
Publisher:
Medcom Limited.
Lee, PPW; Poon, GWK; Kwan, EYW; Wong, KY; Chan, KW; Lee, JSK; Tam, SCF; Lau, E; Tang, MHY; Gu, XF; Low, LCK; Cheung, PT2004181
 
A family with osteoporosis-pseudoglioma syndrome (OPG) due to compound heterozygous mutation of the LRO5 gene
Proceedings/Conference:
26th Annual Meeting of the American Society for Bone & Mineral Research, October 1-5, 2004, Seattle, USA. Journal of Bone and Mineral Research
Jin, L; Lau, HL; Smith, DK; Lau, KS; Cheung, PT; Kwan, EYW; Low, LCK; Kung, AWC2004143
 
Mutation Analysis of the GLUT2 Gene in a Chinese Patient with Fanconi-Bickel Syndrome
Proceedings/Conference:
Ruby Jubilee Scientific Meeting, HK, 24-26 September 2004 (Abstract in Hong Kong Journal of Paediatrics (new series)
Publisher:
Medcom Limited.
Poon, GWK; Cheung, PT; Chen, RT; Kwan, EYW; Low, LCK2004117
 
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 Kong
Journal:
Hong Kong Journal of Paediatrics
Publisher:
Medcom Limited.
Au, RWM; Kwan, EYW; Yeung, LPK; Cheung, PT; Low, LCK2004121
 
Positive Corrleation of Selective IGF-I Genotypes with Idiopathic Short Stature in Chinese Children
Proceedings/Conference:
ENDO 2004, New Orleans, USA, 16-19 June 2004
Man, E; Tan, KCB; Chan, KW; Yeung, LPK; Kwan, EYW; Wong, WHS; Low, LCK; Cheung, PT2004132
 
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