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Results: 1-22 |
Results: 22
Prevalence and genotype distribution of TT virus in various specimen typesfrom thalassaemic patients
Authors: Chan, PKS Chik, KW Li, CK Tang, NLS Ming, MSK Cheung, JLK Ng, KC Yuen, PMP Cheng, AF
Citation: Pks. Chan et al., Prevalence and genotype distribution of TT virus in various specimen typesfrom thalassaemic patients, J VIRAL HEP, 8(4), 2001, pp. 304-309
Association between mu opioid receptor gene polymorphisms and Chinese heroin addicts
Authors: Szeto, CYK Tang, NLS Lee, DTS Stadlin, A
Citation: Cyk. Szeto et al., Association between mu opioid receptor gene polymorphisms and Chinese heroin addicts, NEUROREPORT, 12(6), 2001, pp. 1103-1106
A polymorphism in the coding region of interleukin-13 gene is associated with atopy but not asthma in Chinese children
Authors: Leung, TF Tang, NLS Chan, IHS Li, AM Ha, G Lam, CWK
Citation: Tf. Leung et al., A polymorphism in the coding region of interleukin-13 gene is associated with atopy but not asthma in Chinese children, CLIN EXP AL, 31(10), 2001, pp. 1515-1521
Somatic beta-catenin mutation in gastric carcinoma - an infrequent event that is not specific for microsatellite instability
Authors: Tong, JHM To, KF Ng, EKW Lau, JYW Lee, TL Lo, KW Leung, WK Tang, NLS Chan, FKL Sung, JJY Chung, SCS
Citation: Jhm. Tong et al., Somatic beta-catenin mutation in gastric carcinoma - an infrequent event that is not specific for microsatellite instability, CANCER LETT, 163(1), 2001, pp. 125-130
Reversible renal failure in paroxysmal nocturnal hemoglobinuria
Authors: Chow, KM Lai, FMM Wang, AYM Chan, YL Tang, NLS Li, PKT
Citation: Km. Chow et al., Reversible renal failure in paroxysmal nocturnal hemoglobinuria, AM J KIDNEY, 37(2), 2001, pp. NIL_95-NIL_100
Pathology of fatal human infection associated with avian influenza A H5N1 virus
Authors: To, KF Chan, PKS Chan, KF Lee, WK Lam, WY Wong, KF Tang, NLS Tsang, DNC Sung, RYT Buckley, TA Tam, JS Cheng, AF
Citation: Kf. To et al., Pathology of fatal human infection associated with avian influenza A H5N1 virus, J MED VIROL, 63(3), 2001, pp. 242-246
Prevalence of breast cancer predisposition gene mutations in Chinese womenand guidelines for genetic testing
Authors: Tang, NLS Choy, KW Pang, CP Yeo, W Johnson, PJ
Citation: Nls. Tang et al., Prevalence of breast cancer predisposition gene mutations in Chinese womenand guidelines for genetic testing, CLIN CHIM A, 313(1-2), 2001, pp. 179-185
Overview of common inherited metabolic diseases in a Southern Chinese population of Hong Kong
Authors: Tang, NLS Hui, J Law, LK To, KF Mak, TWL Cheung, KL Vreken, P Wanders, RJA Fok, TF
Citation: Nls. Tang et al., Overview of common inherited metabolic diseases in a Southern Chinese population of Hong Kong, CLIN CHIM A, 313(1-2), 2001, pp. 195-201
Congenital hypertrophy of the retinal pigment epithelium and APC mutationsin two Chinese families with familial adenomatous polyposis
Authors: Pang, CP Keung, JWY Tang, NLS Fan, DSP Lau, JWY Lam, DSC
Citation: Cp. Pang et al., Congenital hypertrophy of the retinal pigment epithelium and APC mutationsin two Chinese families with familial adenomatous polyposis, EYE, 14, 2000, pp. 18-22
Primary carnitine deficiency in the Chinese
Authors: Tang, NLS Hui, J Law, LK To, KF Cheung, KI Magnus, HN Yuen, PMP Fok, TF
Citation: Nls. Tang et al., Primary carnitine deficiency in the Chinese, CHIN MED J, 113(4), 2000, pp. 376-380
Characterization of early IgA nephropathy
Authors: Lai, FMM Szeto, CC Choi, PCL Li, PKT Chan, AWH Tang, NLS Lui, SF Wang, AYM To, KF
Citation: Fmm. Lai et al., Characterization of early IgA nephropathy, AM J KIDNEY, 36(4), 2000, pp. 703-708
Outcome of IgA nephropathy in adults graded by chronic histological lesions
Authors: To, KF Choi, PCL Szeto, CC Li, PKT Tang, NLS Leung, CB Wang, AYM Ho, KKL Wong, TYH Lui, SF Lai, FMM
Citation: Kf. To et al., Outcome of IgA nephropathy in adults graded by chronic histological lesions, AM J KIDNEY, 35(3), 2000, pp. 392-400
New features of renal lesion induced by stroma free hemoglobin
Authors: Chan, WL Tang, NLS Yim, CCW Lai, FM Tam, MSC
Citation: Wl. Chan et al., New features of renal lesion induced by stroma free hemoglobin, TOX PATHOL, 28(5), 2000, pp. 635-642
Application of urine magnesium/creatinine ratio as an indicator for insufficient magnesium intake
Authors: Tang, NLS Chan, YK Hui, E Woo, J
Citation: Nls. Tang et al., Application of urine magnesium/creatinine ratio as an indicator for insufficient magnesium intake, CLIN BIOCH, 33(8), 2000, pp. 675-678
A new recommendation for maternal weight gain in Chinese women
Authors: Wong, W Tang, NLS Lau, TK Wong, TW
Citation: W. Wong et al., A new recommendation for maternal weight gain in Chinese women, J AM DIET A, 100(7), 2000, pp. 791-796
Prevalence of mutations in the BRCA1 gene among Chinese patients with breast cancer
Authors: Tang, NLS Pang, CP Yeo, W Choy, KW Lam, PK Suen, M Law, LK King, WWK Johnson, P Hjelm, M
Citation: Nls. Tang et al., Prevalence of mutations in the BRCA1 gene among Chinese patients with breast cancer, J NAT CANC, 91(10), 1999, pp. 882-885
Classical galactosaemia in Chinese: A case report and review of disease incidence
Authors: Cheung, KL Tang, NLS Hsiao, KJ Law, LK Wong, W Ng, PC Pang, CP Applegarth, DA Fok, TF Hjelm, NM
Citation: Kl. Cheung et al., Classical galactosaemia in Chinese: A case report and review of disease incidence, J PAEDIAT C, 35(4), 1999, pp. 399-400
Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency (vol 8, pg 655, 1999)
Authors: Tang, NLS Ganapathy, V Wu, X Hui, J Seth, P Yuen, PMP Wanders, RJA Fok, TF Hjelm, NM
Citation: Nls. Tang et al., Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency (vol 8, pg 655, 1999), HUM MOL GEN, 8(5), 1999, pp. 943-943
Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency
Authors: Tang, NLS Ganapathy, V Wu, X Hui, J Seth, P Yuen, PMP Fok, TF Hjelm, NM
Citation: Nls. Tang et al., Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency, HUM MOL GEN, 8(4), 1999, pp. 655-660
Severe hypokalemic myopathy in Gitelman's syndrome
Authors: Tang, NLS Hui, J To, KF Ng, HK Hjelm, NM Fok, TF
Citation: Nls. Tang et al., Severe hypokalemic myopathy in Gitelman's syndrome, MUSCLE NERV, 22(4), 1999, pp. 545-547
Detection of fetal-derived paternally inherited X-chromosome polymorphismsin maternal plasma
Authors: Tang, NLS Leung, TN Zhang, J Lau, TK Lo, YMD
Citation: Nls. Tang et al., Detection of fetal-derived paternally inherited X-chromosome polymorphismsin maternal plasma, CLIN CHEM, 45(11), 1999, pp. 2033-2035
Avoiding cardiopulmonary bypass in multivessel CABG reduces cytokine response and myocardial injury
Authors: Wan, S Izzat, MB Lee, TW Wan, IYP Tang, NLS Yim, APC
Citation: S. Wan et al., Avoiding cardiopulmonary bypass in multivessel CABG reduces cytokine response and myocardial injury, ANN THORAC, 68(1), 1999, pp. 52-56
Risultati: 1-22 |