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Results: 1-25 | 26-27
Results: 1-25/27
MOLECULAR DIAGNOSTICS FOR CARDIOVASCULAR-DISEASE
Authors: PANG CP
Citation: Cp. Pang, MOLECULAR DIAGNOSTICS FOR CARDIOVASCULAR-DISEASE, CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 36(8), 1998, pp. 605-614
CGG REPEAT INTERRUPTIONS IN THE FMR1 GENE IN PATIENTS WITH INFANTILE-AUTISM
Authors: POON PMK CHEN QL LAI KYC WONG CK PANG CP
Citation: Pmk. Poon et al., CGG REPEAT INTERRUPTIONS IN THE FMR1 GENE IN PATIENTS WITH INFANTILE-AUTISM, CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 36(8), 1998, pp. 649-653
MUTATIONS IN THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE IN CHINESE FAMILIAL HYPERCHOLESTEROLEMIA PATIENTS
Authors: MAK YT PANG CP TOMLINSON B ZHANG J CHAN YS MAK TWL MASAREI JRL
Citation: Yt. Mak et al., MUTATIONS IN THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE IN CHINESE FAMILIAL HYPERCHOLESTEROLEMIA PATIENTS, Arteriosclerosis, thrombosis, and vascular biology, 18(10), 1998, pp. 1600-1605
POSSIBLE COMMON MUTATIONS IN THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE IN CHINESE
Authors: MAK YT ZHANG J CHAN YS MAK TWL TOMLINSON B MASAREI JRL PANG CP
Citation: Yt. Mak et al., POSSIBLE COMMON MUTATIONS IN THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE IN CHINESE, Human mutation, 1998, pp. 310-313
DETERMINATION OF THE RISK FOR FAMILIAL DISEASE IN RET MUTATION-NEGATIVE PATIENTS WITH MEDULLARY-THYROID CANCER
Authors: TANG NLS YEUNG VTF COCKRAM CS PANG CP
Citation: Nls. Tang et al., DETERMINATION OF THE RISK FOR FAMILIAL DISEASE IN RET MUTATION-NEGATIVE PATIENTS WITH MEDULLARY-THYROID CANCER, Journal of internal medicine, 244(2), 1998, pp. 185-187
RANDOMIZED TRIAL OF THE EFFECT OF SUPPLEMENTATION ON THE COGNITIVE FUNCTION OF OLDER-PEOPLE WITH SUBNORMAL COBALAMIN LEVELS
Authors: KWOK T TANG C WOO J LAI WK LAW LK PANG CP
Citation: T. Kwok et al., RANDOMIZED TRIAL OF THE EFFECT OF SUPPLEMENTATION ON THE COGNITIVE FUNCTION OF OLDER-PEOPLE WITH SUBNORMAL COBALAMIN LEVELS, International journal of geriatric psychiatry, 13(9), 1998, pp. 611-616
RARITY OF DEBRISOQUINE HYDROXYLASE GENE POLYMORPHISM IN CHINESE PATIENTS WITH PARKINSONS-DISEASE
Authors: PANG CP ZHANG J WOO J CHAN D LAW LK TONG SF KWOK T KAY R
Citation: Cp. Pang et al., RARITY OF DEBRISOQUINE HYDROXYLASE GENE POLYMORPHISM IN CHINESE PATIENTS WITH PARKINSONS-DISEASE, Movement disorders, 13(3), 1998, pp. 529-532
LOW-DENSITY-LIPOPROTEIN RECEPTOR-RELATED PROTEIN GENE AMPLIFICATION AND 766T POLYMORPHISM IN ASTROCYTOMAS
Authors: BAUM L DONG ZY CHOY KW PANG CP NG HK
Citation: L. Baum et al., LOW-DENSITY-LIPOPROTEIN RECEPTOR-RELATED PROTEIN GENE AMPLIFICATION AND 766T POLYMORPHISM IN ASTROCYTOMAS, Neuroscience letters, 256(1), 1998, pp. 5-8
LOW-DENSITY-LIPOPROTEIN RECEPTOR-RELATED PROTEIN GENE EXON-3 POLYMORPHISM ASSOCIATION WITH ALZHEIMERS-DISEASE IN CHINESE
Authors: BAUM L CHEN L NG HK CHAN YS MAK YT WOO J CHIU HFK PANG CP
Citation: L. Baum et al., LOW-DENSITY-LIPOPROTEIN RECEPTOR-RELATED PROTEIN GENE EXON-3 POLYMORPHISM ASSOCIATION WITH ALZHEIMERS-DISEASE IN CHINESE, Neuroscience letters, 247(1), 1998, pp. 33-36
NO ASSOCIATION DETECTED BETWEEN VERY-LOW-DENSITY LIPOPROTEIN RECEPTOR(VLDL-R) AND LATE-ONSET ALZHEIMERS-DISEASE IN HONG-KONG CHINESE
Authors: CHEN L BAUM L NG HK CHAN YS MAK YT WOO J CHIU H PANG CP
Citation: L. Chen et al., NO ASSOCIATION DETECTED BETWEEN VERY-LOW-DENSITY LIPOPROTEIN RECEPTOR(VLDL-R) AND LATE-ONSET ALZHEIMERS-DISEASE IN HONG-KONG CHINESE, Neuroscience letters, 241(1), 1998, pp. 33-36
GENETIC AND ENVIRONMENTAL RISK-FACTORS FOR PARKINSONS-DISEASE IN A CHINESE POPULATION
Authors: CHAN DKY WOO J HO SC PANG CP LAW LK NG PW HUNG WT KWOK T HUI E ORR K LEUNG MF KAY R
Citation: Dky. Chan et al., GENETIC AND ENVIRONMENTAL RISK-FACTORS FOR PARKINSONS-DISEASE IN A CHINESE POPULATION, Journal of Neurology, Neurosurgery and Psychiatry, 65(5), 1998, pp. 781-784
FAMILIAL HYPERCHOLESTEROLEMIA IN HONG-KONG
Authors: TOMLINSON B LAN W MAK YT CHAN YS MAK TWL CRITCHLEY JAJH MASEREI JRL PANG CP
Citation: B. Tomlinson et al., FAMILIAL HYPERCHOLESTEROLEMIA IN HONG-KONG, Atherosclerosis, 136, 1998, pp. 49-49
INVESTIGATION OF MUTATIONS AND POLYMORPHISMS IN THE LIPOPROTEIN-LIPASE GENE
Authors: CHAN YS TOMLINSON B MAK YT MAK TWL PANG CP
Citation: Ys. Chan et al., INVESTIGATION OF MUTATIONS AND POLYMORPHISMS IN THE LIPOPROTEIN-LIPASE GENE, Atherosclerosis, 136, 1998, pp. 82-82
A NOVEL DRAL POLYMORPHISM IN THE 3'-UNTRANSLATED REGION OF HUMAN GLUCOSE-6-PHOSPHATASE GENE - USEFUL FOR CARRIER DETECTION AND PRENATAL-DIAGNOSIS OF GLYCOGEN-STORAGE-DISEASE TYPE 1A
Authors: LAM CW LIANG MH PANG CP TONG SF WONG LJC
Citation: Cw. Lam et al., A NOVEL DRAL POLYMORPHISM IN THE 3'-UNTRANSLATED REGION OF HUMAN GLUCOSE-6-PHOSPHATASE GENE - USEFUL FOR CARRIER DETECTION AND PRENATAL-DIAGNOSIS OF GLYCOGEN-STORAGE-DISEASE TYPE 1A, Clinical genetics, 53(6), 1998, pp. 502-503
GLUCOSE-6-PHOSPHATASE GENE (727G-]T) SPLICING MUTATION IS PREVALENT IN HONG-KONG CHINESE PATIENTS WITH GLYCOGEN-STORAGE-DISEASE TYPE 1A
Authors: LAM CW BUT WM SHEK CC TONG SF CHAN YS CHOY KW TSE WY PANG CP HJELM NM
Citation: Cw. Lam et al., GLUCOSE-6-PHOSPHATASE GENE (727G-]T) SPLICING MUTATION IS PREVALENT IN HONG-KONG CHINESE PATIENTS WITH GLYCOGEN-STORAGE-DISEASE TYPE 1A, Clinical genetics, 53(3), 1998, pp. 184-190
VERY-LOW-DENSITY LIPOPROTEIN RECEPTOR (VLDLR) POLYMORPHISM IN HONG-KONG CHINESE WITH LATE-ONSET ALZHEIMERS-DISEASE (AD)
Authors: CHEN L BAUM L NG HK PANG CP
Citation: L. Chen et al., VERY-LOW-DENSITY LIPOPROTEIN RECEPTOR (VLDLR) POLYMORPHISM IN HONG-KONG CHINESE WITH LATE-ONSET ALZHEIMERS-DISEASE (AD), Brain pathology, 7(4), 1997, pp. 1095-1095
LIPID-PEROXIDATION IN CORD-BLOOD AT BIRTH - A MARKER OF FETAL HYPOXIADURING LABOR
Authors: ROGERS MS WANG W MONGELLI M PANG CP DULEY JA CHANG AMZ
Citation: Ms. Rogers et al., LIPID-PEROXIDATION IN CORD-BLOOD AT BIRTH - A MARKER OF FETAL HYPOXIADURING LABOR, Gynecologic and obstetric investigation, 44(4), 1997, pp. 229-233
BIOCHEMICAL INVESTIGATION OF YOUNG HOSPITALIZED CHINESE CHILDREN - RESULTS OVER A 7-YEAR PERIOD
Authors: PANG CP LAW LK MAK YT SHEK CC CHEUNG KL MAK TWL LAM CW CHAN AYW FOK TF
Citation: Cp. Pang et al., BIOCHEMICAL INVESTIGATION OF YOUNG HOSPITALIZED CHINESE CHILDREN - RESULTS OVER A 7-YEAR PERIOD, American journal of medical genetics, 72(4), 1997, pp. 417-421
AN UNUSUAL CASE OF MULTIPLE CARBOXYLASE DEFICIENCY PRESENTING AS GENERALIZED PUSTULAR PSORIASIS IN A CHINESE BOY
Authors: LAW LK LAU CY PANG CP LAM WY SWEETMAN L FOK TF HJELM M
Citation: Lk. Law et al., AN UNUSUAL CASE OF MULTIPLE CARBOXYLASE DEFICIENCY PRESENTING AS GENERALIZED PUSTULAR PSORIASIS IN A CHINESE BOY, Journal of inherited metabolic disease, 20(1), 1997, pp. 106-107
RAPID SCREENING FOR ALPHA(1)-ANTITRYPSIN Z-MUTATION AND S-MUTATION
Authors: LAM CWK PANG CP POON PMK YIN CH BHARATHI G
Citation: Cwk. Lam et al., RAPID SCREENING FOR ALPHA(1)-ANTITRYPSIN Z-MUTATION AND S-MUTATION, Clinical chemistry, 43(2), 1997, pp. 403-404
A NOVEL FRAMESHIFT MUTATION IN GLUCOSE-6-PHOSPHATASE GENE CAUSING VON-GIERKE-DISEASE IN CHINESE
Authors: LAM CW BUT WM CHOY KW SHEK CC PANG CP HJELM NM
Citation: Cw. Lam et al., A NOVEL FRAMESHIFT MUTATION IN GLUCOSE-6-PHOSPHATASE GENE CAUSING VON-GIERKE-DISEASE IN CHINESE, American journal of human genetics, 61(4), 1997, pp. 2311-2311
HYPERHOMOCYSTEINAEMIA AND PREMATURE CORONARY-ARTERY DISEASE IN THE CHINESE
Authors: LOLIN YI SANDERSON JE CHENG SK CHAN CF PANG CP WOO KS MASAREI JRL
Citation: Yi. Lolin et al., HYPERHOMOCYSTEINAEMIA AND PREMATURE CORONARY-ARTERY DISEASE IN THE CHINESE, HEART, 76(2), 1996, pp. 117-122
URINARY D-GLUCARIC ACID EXCRETION IN IDIOPATHIC NEONATAL JAUNDICE
Authors: SUNG RYT PANG CP LYON A LOONG PL DAVIES DP
Citation: Ryt. Sung et al., URINARY D-GLUCARIC ACID EXCRETION IN IDIOPATHIC NEONATAL JAUNDICE, Chinese medical journal, 109(3), 1996, pp. 201-205
APOLIPOPROTEIN-E GENOTYPE AND ALZHEIMERS-DISEASE IN HONG-KONG ELDERLYCHINESE
Authors: MAK YT CHIU H WOO J KAY R CHAN YS HUI E SZE KH LUM C KWOK T PANG CP
Citation: Yt. Mak et al., APOLIPOPROTEIN-E GENOTYPE AND ALZHEIMERS-DISEASE IN HONG-KONG ELDERLYCHINESE, Neurology, 46(1), 1996, pp. 146-149
CORD-BLOOD BIOCHEMISTRY AND IDIOPATHIC NEONATAL JAUNDICE
Authors: LAW LK PANG CP CHEUNG KL FOK TF
Citation: Lk. Law et al., CORD-BLOOD BIOCHEMISTRY AND IDIOPATHIC NEONATAL JAUNDICE, Clinical chemistry, 42(10), 1996, pp. 1716-1717
Risultati: 1-25 | 26-27