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Results: 1-25 | 26-29
Results: 1-25/29
COEXISTENCE OF ANTITHROMBIN DEFICIENCY, FACTOR-V-LEIDEN AND HYPERHOMOCYSTEINEMIA IN A THROMBOTIC FAMILY
Authors: GEMMATI D SERINO ML MORATELLI S MARI R BALLERINI G SCAPOLI GL
Citation: D. Gemmati et al., COEXISTENCE OF ANTITHROMBIN DEFICIENCY, FACTOR-V-LEIDEN AND HYPERHOMOCYSTEINEMIA IN A THROMBOTIC FAMILY, Blood coagulation & fibrinolysis, 9(2), 1998, pp. 173-176
A MODIFIED FUNCTIONAL GLOBAL TEST TO MEASURE PROTEIN-C, PROTEIN-S ACTIVITIES AND THE ACTIVATED PROTEIN C-RESISTANCE PHENOTYPE
Authors: GEMMATI D SERINO ML SCAPOLI GL
Citation: D. Gemmati et al., A MODIFIED FUNCTIONAL GLOBAL TEST TO MEASURE PROTEIN-C, PROTEIN-S ACTIVITIES AND THE ACTIVATED PROTEIN C-RESISTANCE PHENOTYPE, Thrombosis research, 92(3), 1998, pp. 141-148
LOW FOLATE LEVELS AND THERMOLABILE MTHFR AS PRIMARY DETERMINANT OF MILD HYPERHOMOCYSTEINEMIA IN NORMAL AND THROMBOEMBOLIC SUBJECTS
Authors: GEMMATI D SERINO ML MORATELLI S MARI R FIORINI S BIGNARDI M SCAPOLI GL
Citation: D. Gemmati et al., LOW FOLATE LEVELS AND THERMOLABILE MTHFR AS PRIMARY DETERMINANT OF MILD HYPERHOMOCYSTEINEMIA IN NORMAL AND THROMBOEMBOLIC SUBJECTS, Thrombosis research, 91(3), 1998, pp. 120-120
A MODIFIED FUNCTIONAL GLOBAL TEST TO MEASURE PC, PS ACTIVITIES AND THE APC-RESISTANCE PHENOTYPE
Authors: GEMMATI D SERINO ML MARI R MORATELLI S BIGNARDI M FIORINI S SCAPOLI GL
Citation: D. Gemmati et al., A MODIFIED FUNCTIONAL GLOBAL TEST TO MEASURE PC, PS ACTIVITIES AND THE APC-RESISTANCE PHENOTYPE, Thrombosis research, 91(3), 1998, pp. 121-121
DIFFERENT ANTICOAGULANT RESPONSE TO ACTIVATED PROTEIN-C (APC TEST) AND TO AGKISTRODON CONTORTIX VENOM (ACV TEST) IN A FAMILY WITH FV-R506Q SUBSTITUTION
Authors: GEMMATI D SERINO ML MARI R VERZOLA I MORATELLI S BALLERINI G
Citation: D. Gemmati et al., DIFFERENT ANTICOAGULANT RESPONSE TO ACTIVATED PROTEIN-C (APC TEST) AND TO AGKISTRODON CONTORTIX VENOM (ACV TEST) IN A FAMILY WITH FV-R506Q SUBSTITUTION, Clinical and applied thrombosis/hemostasis, 3(3), 1997, pp. 168-173
RESISTANCE TO ACTIVATED PROTEIN-C AND LOW-LEVELS OF PROTEIN-S ACTIVITY IN 9 THROMBOPHILIC FAMILIES - A CORRECT DIAGNOSIS
Authors: GEMMATI D SERINO ML VERZOLA I MARI R MORATELLI S BALLERINI G
Citation: D. Gemmati et al., RESISTANCE TO ACTIVATED PROTEIN-C AND LOW-LEVELS OF PROTEIN-S ACTIVITY IN 9 THROMBOPHILIC FAMILIES - A CORRECT DIAGNOSIS, Blood coagulation & fibrinolysis, 8(2), 1997, pp. 118-123
DIFFERENT ANTICOAGULANT RESPONSE TO ACTIVATED PROTEIN-C (APC-TEST) AND TO AGKISTRODON CONTORTIX VENOM (ACV-TEST) IN A FAMILY WITH FV-R506Q SUBSTITUTION
Authors: GEMMATI D VERZOLA I MARI R SERINO ML MORATELLI S BALLERINI G
Citation: D. Gemmati et al., DIFFERENT ANTICOAGULANT RESPONSE TO ACTIVATED PROTEIN-C (APC-TEST) AND TO AGKISTRODON CONTORTIX VENOM (ACV-TEST) IN A FAMILY WITH FV-R506Q SUBSTITUTION, Thrombosis and haemostasis, 1997, pp. 86-86
A DE-NOVO ANTITHROMBIN MUTATION FOUND IN A PATIENT WITH DEEP-VEIN THROMBOSIS AND VASCULAR ABNORMALITIES
Authors: DIIASIO MG GEMMATI D MICHELETTI F SERINO ML MORATELLI S BALLERINI G BERNARDI F
Citation: Mg. Diiasio et al., A DE-NOVO ANTITHROMBIN MUTATION FOUND IN A PATIENT WITH DEEP-VEIN THROMBOSIS AND VASCULAR ABNORMALITIES, Thrombosis and haemostasis, 1997, pp. 1761-1761
COEXISTENCE OF ANTITRHOMBIN DEFICIENCY, FACTOR-V-LEIDEN AND HEREDITARY HYPERHOMOCYST(E)INEMIA IN A THROMBOTIC FAMILY
Authors: GEMMATI D MARI R VERZOLA I MORATELLI S BALLERINI G SERINO ML
Citation: D. Gemmati et al., COEXISTENCE OF ANTITRHOMBIN DEFICIENCY, FACTOR-V-LEIDEN AND HEREDITARY HYPERHOMOCYST(E)INEMIA IN A THROMBOTIC FAMILY, Thrombosis and haemostasis, 1997, pp. 2164-2164
DETECTION OF NEW POLYMORPHIC MARKERS IN THE FACTOR-V GENE - ASSOCIATION WITH FACTOR-V LEVELS IN PLASMA
Authors: LUNGHI B IACOVIELLO L GEMMATI D DILASIO MG CASTOLDI E PINOTTI M CASTAMAN G REDAELLI R MARIANI G MARCHETTI G BERNARDI F
Citation: B. Lunghi et al., DETECTION OF NEW POLYMORPHIC MARKERS IN THE FACTOR-V GENE - ASSOCIATION WITH FACTOR-V LEVELS IN PLASMA, Thrombosis and haemostasis, 75(1), 1996, pp. 45-48
A NOVEL MUTATION (LEU817PRO) CAUSING TYPE 2A VON-WILLEBRAND DISEASE
Authors: GEMMATI D SERINO ML MORATELLI S BALLERINI G FURBETTA M LUNGHI B MARCHETTI G BERNARDI F
Citation: D. Gemmati et al., A NOVEL MUTATION (LEU817PRO) CAUSING TYPE 2A VON-WILLEBRAND DISEASE, British Journal of Haematology, 92(1), 1996, pp. 241-243
ANTICARDIOLIPIN ANTIBODY-RELATED THROMBOCYTOPENIA - PERSISTENT REMISSION AFTER SPLENECTOMY
Authors: BALLERINI G GEMMATI D MORATELLI S MORELLI P SERINO ML
Citation: G. Ballerini et al., ANTICARDIOLIPIN ANTIBODY-RELATED THROMBOCYTOPENIA - PERSISTENT REMISSION AFTER SPLENECTOMY, Haematologica, 80(3), 1995, pp. 248-251
INCREASED SUSCEPTIBILITY TO PROTEASES IN TYPE-2A VON-WILLEBRAND DISEASE-ASSOCIATED WITH 2 NOVEL MUTATIONS (VAL867GLU, PRO864HIS)
Authors: CASONATO A GEMMATI D LUNGHI B BIZZARO N GIROLAMI A VERZOLA I BERNARDI F
Citation: A. Casonato et al., INCREASED SUSCEPTIBILITY TO PROTEASES IN TYPE-2A VON-WILLEBRAND DISEASE-ASSOCIATED WITH 2 NOVEL MUTATIONS (VAL867GLU, PRO864HIS), Thrombosis and haemostasis, 73(6), 1995, pp. 1171-1171
AN ITALIAN FAMILY WITH A NOVEL MUTATION CAUSING TYPE-2A VW DISEASE AND WITH REDUCED LEVELS OF VWF NOT LINKED WITH THE VWF GENE
Authors: GEMMATI D SERINO ML MORATELLI S BALLERINI G FURBETTA M LUNGHI B MARCHETTI G BERNARDI F
Citation: D. Gemmati et al., AN ITALIAN FAMILY WITH A NOVEL MUTATION CAUSING TYPE-2A VW DISEASE AND WITH REDUCED LEVELS OF VWF NOT LINKED WITH THE VWF GENE, Thrombosis and haemostasis, 73(6), 1995, pp. 1171-1171
DETECTION OF NEW POLYMORPHIC MARKERS IN THE FACTOR-V GENE
Authors: BERNARDI F LUNGHI B DILASIO MG CASTOLDI E PINOTTI M GEMMATI D MARCHETTI G
Citation: F. Bernardi et al., DETECTION OF NEW POLYMORPHIC MARKERS IN THE FACTOR-V GENE, Thrombosis and haemostasis, 73(6), 1995, pp. 1366-1366
A PHOTOMETRIC-METHOD FOR THE DOSAGE OF FACTOR-XIII APPLIED TO THE STUDY OF CHRONIC HEPATOPATHIES
Authors: BALLERINI G GEMMATI D MORATELLI S MORELLI P SERINO ML
Citation: G. Ballerini et al., A PHOTOMETRIC-METHOD FOR THE DOSAGE OF FACTOR-XIII APPLIED TO THE STUDY OF CHRONIC HEPATOPATHIES, Thrombosis research, 78(5), 1995, pp. 451-456
MOLECULAR DEFECTS IN CRM-VII DEFICIENCIES - MODELING OF MISSENSE MUTATIONS IN THE CATALYTIC DOMAIN OF FVII( FACTOR)
Authors: BERNARDI F LINEY DL PATRACCHINI P GEMMATI D LEGNANI C ARCIERI P PINOTTI M REDAELLI R BALLERINI G PEMBERTON S WACEY AI MARIANI G TUDDENHAM EGD MARCHETTI G
Citation: F. Bernardi et al., MOLECULAR DEFECTS IN CRM-VII DEFICIENCIES - MODELING OF MISSENSE MUTATIONS IN THE CATALYTIC DOMAIN OF FVII( FACTOR), British Journal of Haematology, 86(3), 1994, pp. 610-618
IN-FRAME DELETION OF VONWILLEBRAND FACTOR-A DOMAINS IN A DOMINANT TYPE OF VONWILLEBRAND DISEASE
Authors: BERNARDI F PATRACCHINI P GEMMATI D PINOTTI M SCHWIENBACHER C BALLERINI G MARCHETTI G
Citation: F. Bernardi et al., IN-FRAME DELETION OF VONWILLEBRAND FACTOR-A DOMAINS IN A DOMINANT TYPE OF VONWILLEBRAND DISEASE, Human molecular genetics, 2(5), 1993, pp. 545-548
MOLECULAR ANALYSIS OF FACTOR-VII DEFICIENCY IN ITALY - A FREQUENT MUTATION (FVII-LAZIO) IN A REPEATED INTRONIC REGION
Authors: BERNARDI F PATRACCHINI P GEMMATI D FERRATI M ARCIERI P PAPACCHINI M REDAELLI R BAUDO F MARIANI G MARCHETTI G
Citation: F. Bernardi et al., MOLECULAR ANALYSIS OF FACTOR-VII DEFICIENCY IN ITALY - A FREQUENT MUTATION (FVII-LAZIO) IN A REPEATED INTRONIC REGION, Human genetics, 92(5), 1993, pp. 446-450
TYPE-II PROTEIN-C DEFICIENCY CAUSED BY A MISSENSE MUTATION (GLY 381 GREATER-THAN SER) IN THE SUBSTRATE-BINDING POCKET
Authors: MARCHETTI G PATRACCHINI P GEMMATI D CASTAMAN G RODEGHIERO F WACEY A COOPER DN TUDDENHAM EGD BERNARDI F
Citation: G. Marchetti et al., TYPE-II PROTEIN-C DEFICIENCY CAUSED BY A MISSENSE MUTATION (GLY 381 GREATER-THAN SER) IN THE SUBSTRATE-BINDING POCKET, Thrombosis and haemostasis, 69(6), 1993, pp. 722-722
DETECTION OF A PROTEIN-C GENE MUTATION PRESENT IN THE ASYMPTOMATIC AND NOT IN THE THROMBOSIS-PRONE LINEAGE
Authors: GEMMATI D PATRACCHINI P MARCHETTI G SERINO ML MORATELLI S GUERRA S BALLERINI G BERNARDI F
Citation: D. Gemmati et al., DETECTION OF A PROTEIN-C GENE MUTATION PRESENT IN THE ASYMPTOMATIC AND NOT IN THE THROMBOSIS-PRONE LINEAGE, Thrombosis and haemostasis, 69(6), 1993, pp. 1253-1253
MOLECULAR DEFECTS IN CONGENITAL FACTOR-VII DEFICIENCIES
Authors: BERNARDI F PATRACCHINI P GEMMATI D PINOTTI M BAUDO F DEROSA V MARIANI G MARCHETTI G
Citation: F. Bernardi et al., MOLECULAR DEFECTS IN CONGENITAL FACTOR-VII DEFICIENCIES, Thrombosis and haemostasis, 69(6), 1993, pp. 1292-1292
DELETION OF EXONS 26-34 (DOMAIN D3-A3) OF VONWILLEBRAND-FACTOR GENE IN THE VONWILLEBRAND DISEASE TYPE-II
Authors: PATRACCHINI P MARCHETTI G GEMMATI D SERINO ML BALLERINI G BERNARDI F
Citation: P. Patracchini et al., DELETION OF EXONS 26-34 (DOMAIN D3-A3) OF VONWILLEBRAND-FACTOR GENE IN THE VONWILLEBRAND DISEASE TYPE-II, Thrombosis research, 70, 1993, pp. 19-19
DETECTION AND CHARACTERIZATION OF POLYMORPHIC MARKERS IN THE FACTOR-VII GENE
Authors: GEMMATI D MARCHETTI G PATRACCHINI P PAPACCHINI P PINOTTI M ARCIERI P MARIANI G BERNARDI F
Citation: D. Gemmati et al., DETECTION AND CHARACTERIZATION OF POLYMORPHIC MARKERS IN THE FACTOR-VII GENE, Thrombosis research, 70, 1993, pp. 19-19
CHARACTERIZATION OF MOLECULAR LESIONS CAUSING PROTEIN-C DEFICIENCY (TYPE-I AND TYPE-II)
Authors: MARCHETTI G GEMMATI D PATRACCHINI P CASTAMAN G MORATELLI S PALARETI G RODEGHIERO F BALLERINI G BERNARDI F
Citation: G. Marchetti et al., CHARACTERIZATION OF MOLECULAR LESIONS CAUSING PROTEIN-C DEFICIENCY (TYPE-I AND TYPE-II), Thrombosis research, 70, 1993, pp. 20-20
Risultati: 1-25 | 26-29