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Results: 1-25/103
PAI-1 PLASMA-LEVELS IN A GENERAL-POPULATION WITHOUT CLINICAL-EVIDENCEOF ATHEROSCLEROSIS - RELATION TO ENVIRONMENTAL AND GENETIC-DETERMINANTS
Authors: MARGAGLIONE M CAPPUCCI G DADDEDDA M COLAIZZO D GIULIANI N VECCHIONE G MASCOLO G GRANDONE E DIMINNO G
Citation: M. Margaglione et al., PAI-1 PLASMA-LEVELS IN A GENERAL-POPULATION WITHOUT CLINICAL-EVIDENCEOF ATHEROSCLEROSIS - RELATION TO ENVIRONMENTAL AND GENETIC-DETERMINANTS, Arteriosclerosis, thrombosis, and vascular biology, 18(4), 1998, pp. 562-567
THE PAI-1 GENE LOCUS 4G 5G POLYMORPHISM IS ASSOCIATED WITH A FAMILY HISTORY OF CORONARY-ARTERY DISEASE/
Authors: MARGAGLIONE M CAPPUCCI G COLAIZZO D GIULIANI N VECCHIONE G GRANDONE E PENNELLI O DIMINNO G
Citation: M. Margaglione et al., THE PAI-1 GENE LOCUS 4G 5G POLYMORPHISM IS ASSOCIATED WITH A FAMILY HISTORY OF CORONARY-ARTERY DISEASE/, Arteriosclerosis, thrombosis, and vascular biology, 18(2), 1998, pp. 152-156
FIBRINOGEN PLASMA-LEVELS IN AN APPARENTLY HEALTHY GENERAL-POPULATION - RELATION TO ENVIRONMENTAL AND GENETIC-DETERMINANTS
Authors: MARGAGLIONE M CAPPUCCI G COLAIZZO D PIRRO L VECCHIONE G GRANDONE E DIMINNO G
Citation: M. Margaglione et al., FIBRINOGEN PLASMA-LEVELS IN AN APPARENTLY HEALTHY GENERAL-POPULATION - RELATION TO ENVIRONMENTAL AND GENETIC-DETERMINANTS, Thrombosis and haemostasis, 80(5), 1998, pp. 805-810
RETINAL VEIN OCCLUSION AND INHERITED CONDITIONS PREDISPOSING TO THROMBOPHILIA
Authors: ALBISINNI R COPPOLA A LOFFREDO M CERBONE AM DIMINNO G GRECO GM
Citation: R. Albisinni et al., RETINAL VEIN OCCLUSION AND INHERITED CONDITIONS PREDISPOSING TO THROMBOPHILIA, Thrombosis and haemostasis, 80(4), 1998, pp. 702-703
THE METHYLENETETRAHYDROFOLATE REDUCTASE TT677 GENOTYPE IS ASSOCIATED WITH VENOUS THROMBOSIS INDEPENDENTLY OF THE COEXISTENCE OF THE FV LEIDEN AND THE PROTHROMBIN A(20210) MUTATION
Authors: MARGAGLIONE M DANDREA G DADDEDDA M GIULIANI N CAPPUCCI G IANNACCONE L VECCHIONE G GRANDONE E BRANCACCIO V DIMINNO G
Citation: M. Margaglione et al., THE METHYLENETETRAHYDROFOLATE REDUCTASE TT677 GENOTYPE IS ASSOCIATED WITH VENOUS THROMBOSIS INDEPENDENTLY OF THE COEXISTENCE OF THE FV LEIDEN AND THE PROTHROMBIN A(20210) MUTATION, Thrombosis and haemostasis, 79(5), 1998, pp. 907-911
METHYLENE TETRAHYDROFOLATE REDUCTASE (MTHFR) 677T-]C MUTATION AND UNEXPLAINED EARLY-PREGNANCY LOSS
Authors: GRANDONE E MARGAGLIONE M COLAIZZO D DADDEDDA M DANDREA G PAVONE G DIMINNO G
Citation: E. Grandone et al., METHYLENE TETRAHYDROFOLATE REDUCTASE (MTHFR) 677T-]C MUTATION AND UNEXPLAINED EARLY-PREGNANCY LOSS, Thrombosis and haemostasis, 79(5), 1998, pp. 1056-1057
INFLUENCE OF CARDIOVASCULAR RISK-FACTORS ON RELATION BETWEEN ANGIOTENSIN-CONVERTING ENZYME-GENE POLYMORPHISM AND BLOOD-PRESSURE IN ARTERIAL-HYPERTENSION
Authors: CELENTANO A MANCINI FP CRIVARO M PALMIERI V DESTEFANO V FERRARA LA DIMINNO G DESIMONE G
Citation: A. Celentano et al., INFLUENCE OF CARDIOVASCULAR RISK-FACTORS ON RELATION BETWEEN ANGIOTENSIN-CONVERTING ENZYME-GENE POLYMORPHISM AND BLOOD-PRESSURE IN ARTERIAL-HYPERTENSION, Journal of hypertension, 16(7), 1998, pp. 985-991
IDENTIFYING HUMAN PLATELET GLYCOPROTEINS IIB AND IIIA BY CAPILLARY-ELECTROPHORESIS
Authors: VECCHIONE G MARGAGLIONE M GRANDONE E COLAIZZO D CAPPUCCI G GIULIANI N DADDEDDA M DANDREA G NOBILE M AMORIELLO A DIMINNO G
Citation: G. Vecchione et al., IDENTIFYING HUMAN PLATELET GLYCOPROTEINS IIB AND IIIA BY CAPILLARY-ELECTROPHORESIS, Electrophoresis, 19(8-9), 1998, pp. 1468-1474
INCREASED THROMBOTIC RISK FOR PATIENTS WITH ASSOCIATED 844INS68 MUTATION OF THE CBS GENE AND THE 677C-]T MUTATION OF THE MTHFR GENE
Authors: DEFRANCHIS R BUONINCONTI A FERMO I SEBASTIO G SPERANDEO MP MAZZOLA G CERBONE AM SORIENTE L OREFICE G DIMINNO G DANGELO A ANDRIA G
Citation: R. Defranchis et al., INCREASED THROMBOTIC RISK FOR PATIENTS WITH ASSOCIATED 844INS68 MUTATION OF THE CBS GENE AND THE 677C-]T MUTATION OF THE MTHFR GENE, Thrombosis research, 91(3), 1998, pp. 1-1
HYPERHOMOCYSTEINEMIA, VITAMIN STATUS AND HOMOZYGOUS C677T MUTATION OFTHE 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) GENE IN PATIENTSWITH EARLY-ONSET THROMBOTIC EVENTS
Authors: MADONNA P COPPOLA A PAGANO A FERMO I MAZZOLA G CERBONE AM CIRILLO F DANGELO SV DANGELO A DIMINNO G
Citation: P. Madonna et al., HYPERHOMOCYSTEINEMIA, VITAMIN STATUS AND HOMOZYGOUS C677T MUTATION OFTHE 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) GENE IN PATIENTSWITH EARLY-ONSET THROMBOTIC EVENTS, Thrombosis research, 91(3), 1998, pp. 184-184
RAISED IN-VIVO THROMBOXANE BIOSYNTHESIS IN HETEROZYGOTES FOR CYSTATHIONINE-BETA-SYNTHASE DEFICIENCY - SIMILARITIES AND HOMOZYGOUS STATE
Authors: COPPOLA A DAVI G PIEMONTINO U ALBISINNI R GAROFANO T PATRONO C DIMINNO G
Citation: A. Coppola et al., RAISED IN-VIVO THROMBOXANE BIOSYNTHESIS IN HETEROZYGOTES FOR CYSTATHIONINE-BETA-SYNTHASE DEFICIENCY - SIMILARITIES AND HOMOZYGOUS STATE, Thrombosis research, 91(3), 1998, pp. 185-185
VITAMIN-E AND PROBUCOL-SENSITIVE MECHANISMS IN THE ABNORMALLY HIGH THROMBOXANE BIOSYNTHESIS IN HOMOCYSTINURIA DUE TO HOMOZYGOUS CYSTATIONINE-BETA-SYNTHASE DEFICIENCY
Authors: COPPOLA A CERBONE AM GUIOTTO G RUGIADA F DELLAVALLE P DANGELO A DAVI G DIMINNO G PATRONO C
Citation: A. Coppola et al., VITAMIN-E AND PROBUCOL-SENSITIVE MECHANISMS IN THE ABNORMALLY HIGH THROMBOXANE BIOSYNTHESIS IN HOMOCYSTINURIA DUE TO HOMOZYGOUS CYSTATIONINE-BETA-SYNTHASE DEFICIENCY, Thrombosis research, 91(3), 1998, pp. 186-186
HYPERCOAGULABLE STATE AND RETINAL VEIN-THROMBOSIS - A ROLE FOR FACTOR-V-LEIDEN AND THE G20210 MUTATION OF THE PROTHROMBIN GENE
Authors: ALBISINNI R COPPOLA A CIRILLO F GAROFANO T RUGIADA F GRECO GM CERBONE AM DIMINNO G
Citation: R. Albisinni et al., HYPERCOAGULABLE STATE AND RETINAL VEIN-THROMBOSIS - A ROLE FOR FACTOR-V-LEIDEN AND THE G20210 MUTATION OF THE PROTHROMBIN GENE, Thrombosis research, 91(3), 1998, pp. 187-187
HYPERHOMOCYSTEINEMIA AND HOMOZYGOUS C677 MUTATION OF THE 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE GENE IN EARLY-ONSET ISCHEMIC STROKE
Authors: SORIENTE L COPPOLA A MADONNA P CIRILLO F MAZZOLA G DESTEFANO V CERBONE AM OREFICE G DANGELO A DIMINNO G
Citation: L. Soriente et al., HYPERHOMOCYSTEINEMIA AND HOMOZYGOUS C677 MUTATION OF THE 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE GENE IN EARLY-ONSET ISCHEMIC STROKE, Thrombosis research, 91(3), 1998, pp. 188-188
ENDOTHELIN ABNORMALITIES IN PATIENTS WITH PULMONARY-EMBOLISM
Authors: ALBISINNI R SOFIA M MICCO A SORIENTE L FARAONE S ALIFANO M CERBONE AM DIMINNO G
Citation: R. Albisinni et al., ENDOTHELIN ABNORMALITIES IN PATIENTS WITH PULMONARY-EMBOLISM, Thrombosis research, 91(3), 1998, pp. 189-189
METHIONINE INTOLERANCE IS AN INDEPENDENT RISK FACTOR FOR EARLY-ONSET VENOUS THROMBOEMBOLIC DISEASES
Authors: DANGELO A FERMO I MAZZOLA G PARONI R DIMINNO G CRIPPA L VIGANODANGELO S
Citation: A. Dangelo et al., METHIONINE INTOLERANCE IS AN INDEPENDENT RISK FACTOR FOR EARLY-ONSET VENOUS THROMBOEMBOLIC DISEASES, Thrombosis research, 91(3), 1998, pp. 194-194
PERSISTENT TOTAL PLASMA HOMOCYSTEINE REDUCTION AND FOLATE ACCUMULATION FOLLOWING ONE MONTH COURSE OF METHYLTETRAHYDROFOLATE (PREFOLIC(R)) ADMINISTRATION IN PATIENTS WITH MODERATE HYPERHOMOCYSTEINEMIA, THROMBOSIS, AND THE THERMOLABILE MTHFR VARIANT
Authors: DANGELO A COPPOLA A FERMO I MAZZOLA G SORIENTE L GUIOTTO G PARONI R CERBONE AM CRIPPA L DIMINNO G
Citation: A. Dangelo et al., PERSISTENT TOTAL PLASMA HOMOCYSTEINE REDUCTION AND FOLATE ACCUMULATION FOLLOWING ONE MONTH COURSE OF METHYLTETRAHYDROFOLATE (PREFOLIC(R)) ADMINISTRATION IN PATIENTS WITH MODERATE HYPERHOMOCYSTEINEMIA, THROMBOSIS, AND THE THERMOLABILE MTHFR VARIANT, Thrombosis research, 91(3), 1998, pp. 195-195
FROZEN-THAWED PLATELET-DERIVED PHOSPHOLIPIDS AS A CONFIRMATORY TEST FOR THE DIAGNOSIS OF LUPUS ANTICOAGULANTS
Authors: CAPPUCCI G GRANDONE E GIULIANI N VECCHIONE G COLAIZZO D DANDREA G DELPOPOLO A MARGAGLIONE M DIMINNO G
Citation: G. Cappucci et al., FROZEN-THAWED PLATELET-DERIVED PHOSPHOLIPIDS AS A CONFIRMATORY TEST FOR THE DIAGNOSIS OF LUPUS ANTICOAGULANTS, Thrombosis research, 91(3), 1998, pp. 218-218
CLINICAL-FEATURES IN HOMOZYGOUS FOR FACTOR-V-LEIDEN OR PROTHROMBIN A(20210) ALLELE
Authors: BRANCACCIO V DANDREA G IANNACCONE L CIAMPA A CAPPUCCI G COLAIZZO D VECCHIONE G DELPOPOLO A GIULIANI N MARGAGLIONE M DIMINNO G
Citation: V. Brancaccio et al., CLINICAL-FEATURES IN HOMOZYGOUS FOR FACTOR-V-LEIDEN OR PROTHROMBIN A(20210) ALLELE, Thrombosis research, 91(3), 1998, pp. 219-219
UNEXPLAINED EARLY-PREGNANCY LOSS AND METHYLENE TETHRAHYDROFOLATE REDUCTASE (MTHFR) GENE 677T-GREATER-THAN-C MUTATION
Authors: COLAIZZO D GRANDONE E DANDREA G CAPPUCCI G VECCHIONE G GIULIANI N MONTANARO S CHECOLA G CIAVARELLA G PAVONE G MARGAGLIONE M DIMINNO G
Citation: D. Colaizzo et al., UNEXPLAINED EARLY-PREGNANCY LOSS AND METHYLENE TETHRAHYDROFOLATE REDUCTASE (MTHFR) GENE 677T-GREATER-THAN-C MUTATION, Thrombosis research, 91(3), 1998, pp. 220-220
PREVALENCE OF THE 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE MUTATION IN ITALIAN FAMILIES IN WHICH A NEURAL-TUBE DEFECT OCCURS
Authors: COLAIZZO D GRANDONE E CAPPUCCI G GIULIANI N VECCHIONE G PELLEGRINO M ZELANTE L MARTINELLI P SALVIATI M MARGAGLIONE M DIMINNO G
Citation: D. Colaizzo et al., PREVALENCE OF THE 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE MUTATION IN ITALIAN FAMILIES IN WHICH A NEURAL-TUBE DEFECT OCCURS, Thrombosis research, 91(3), 1998, pp. 221-221
IDENTIFICATION OF 3 NOVEL MUTATIONS IN HEREDITARY PROTEIN-S DEFICIENCY
Authors: DANDREA G IANNACCONE L GRANDONE E CAPPUCCI G GIULIANI N BRANCACCIO V MARGAGLIONE M DIMINNO G
Citation: G. Dandrea et al., IDENTIFICATION OF 3 NOVEL MUTATIONS IN HEREDITARY PROTEIN-S DEFICIENCY, Thrombosis research, 91(3), 1998, pp. 222-222
DETECTION OF A NEW POLYMORPHISM IN THE HUMAN PROTHROMBIN GENE
Authors: DANDREA G IANNACCONE L ELVIRA G CAPPUCCI G GIULIANI N BRANCACCIO V MARGAGLIONE M DIMINNO G
Citation: G. Dandrea et al., DETECTION OF A NEW POLYMORPHISM IN THE HUMAN PROTHROMBIN GENE, Thrombosis research, 91(3), 1998, pp. 223-223
ALLELE AND GENOTYPE FREQUENCIES OF GENETIC POLYMORPHISMS OF A SERIES OF PROTEINS INVOLVED IN BLOOD-COAGULATION AND ATHEROSCLEROSIS IN A LARGE ITALIAN GENERAL-POPULATION
Authors: DELPOPOLO A CAPPUCCI G COLAIZZO D DANDREA G GIULIANI N GENNARO V SERIPA D ELVIRA G MARGAGLIONE M DIMINNO G
Citation: A. Delpopolo et al., ALLELE AND GENOTYPE FREQUENCIES OF GENETIC POLYMORPHISMS OF A SERIES OF PROTEINS INVOLVED IN BLOOD-COAGULATION AND ATHEROSCLEROSIS IN A LARGE ITALIAN GENERAL-POPULATION, Thrombosis research, 91(3), 1998, pp. 224-224
COEXISTENCE OF FACTOR-V-LEIDEN AND PROTHROMBIN A20210 MUTATIONS AS ANINFREQUENT BUT A HIGH-RISK CONDITION FOR VENOUS THROMBOEMBOLISM
Authors: GIULIANI N DANDREA G IANNACCONE L GRANDONE E CAPPUCCI G COLAIZZO D VECCHIONE G DELPOPOLO A BRANCACCIO V MARGAGLIONE M DIMINNO G
Citation: N. Giuliani et al., COEXISTENCE OF FACTOR-V-LEIDEN AND PROTHROMBIN A20210 MUTATIONS AS ANINFREQUENT BUT A HIGH-RISK CONDITION FOR VENOUS THROMBOEMBOLISM, Thrombosis research, 91(3), 1998, pp. 225-225
Risultati: 1-25 | 26-50 | 51-75 | 76-100 | >>