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KALAFATIS M
LUNGHI B
SIMIONI P
IOANNOU PA
PETIO M
GIROLAMI A
MANN KG
BERNARDI F
Citation: E. Castoldi et al., MOLECULAR-BASES OF PSEUDO-HOMOZYGOUS APC RESISTANCE - THE COMPOUND HETEROZYGOSITY FOR FV R506Q AND A FV NULL MUTATION RESULTS IN THE EXCLUSIVE PRESENCE OF FV LEIDEN MOLECULES IN PLASMA, Thrombosis and haemostasis, 80(3), 1998, pp. 403-406
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LUNGHI B
CASTOLDI E
MINGOZZI F
BERNARDI F
CASTAMAN G
Citation: B. Lunghi et al., A NOVEL FACTOR-V NULL MUTATION DETECTED IN A THROMBOPHILIC PATIENT WITH PSEUDO-HOMOZYGOUS APC RESISTANCE AND IN AN ASYMPTOMATIC UNRELATED SUBJECT, Blood, 92(4), 1998, pp. 1463-1464
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LUNGHI B
CASTOLDI E
MINGOZZI F
BERNARDI F
Citation: B. Lunghi et al., A NEW FACTOR-V GENE POLYMORPHISM (HIS-1254-ARG) PRESENT IN SUBJECTS OF AFRICAN ORIGIN MIMICS THE R2 POLYMORPHISM (HIS-1299-ARG), Blood, 91(1), 1998, pp. 364-365
Authors:
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CELLI A
LUNGHI B
RAUGEI G
MODESTI A
TREVES C
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Citation: C. Legnani et al., ACTIVATED PROTEIN-C RESISTANCE (APCR) ASSESSMENT IN SAMPLES OF PATIENTS WITH LUPUS ANTICOAGULANT (LAC), Thrombosis and haemostasis, 1997, pp. 89-89
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CASTOLDI E
LUNGHI B
CASTAMAN G
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Citation: F. Bernardi et al., A FACTOR-V GENETIC COMPONENT OTHER THAN THE LEIDEN MUTATION IS ASSOCIATED WITH APC RESISTANCE, Thrombosis and haemostasis, 1997, pp. 670-670
Authors:
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FIORINI S
LUNGHI B
MARCHETTI G
LONGO G
MORFINI M
BERNARDI F
Citation: S. Cinotti et al., A NEW HOMOZYGOUS MUTATION (GLU19ALA) IN THE GLA DOMAIN CAUSES A CRMRED SYMPTOMATIC FACTOR-X DEFICIENCY, Thrombosis and haemostasis, 1997, pp. 1616-1616
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KALAFATIS M
SIMIONI P
LUNGHI B
MANN KG
GIROLAMI A
BERNARDI F
Citation: D. Tormene et al., FACTOR-V AND FACTOR-V MESSENGER-RNA IN PSEUDO-HOMOZYGOUS ACTIVATED PROTEIN-C (APC) RESISTANCE, Thrombosis and haemostasis, 1997, pp. 2440-2440
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LUNGHI B
MARCHETTI G
BERNARDI F
Citation: E. Castoldi et al., NEW POLYMORPHIC MARKERS IN THE FACTOR-V GENE DEFINE A SINGLE AND RAREHAPLOTYPE UNDERLYING THE LEIDEN MUTATION IN THE ITALIAN POPULATION, Thrombosis and haemostasis, 1997, pp. 2511-2511
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LUNGHI B
MINGOZZI F
IOANNOU P
MARCHETTI G
BERNARDI F
Citation: E. Castoldi et al., NEW COAGULATION-FACTOR-V GENE POLYMORPHISMS DEFINE A SINGLE AND INFREQUENT HAPLOTYPE UNDERLYING THE FACTOR-V-LEIDEN MUTATION IN MEDITERRANEAN POPULATIONS AND INDIANS, Thrombosis and haemostasis, 78(3), 1997, pp. 1037-1041
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LUNGHI B
MISSIAGLIA E
BERNARDI F
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Citation: G. Castaman et al., PHENOTYPIC HOMOZYGOUS ACTIVATED PROTEIN-C RESISTANCE-ASSOCIATED WITH COMPOUND HETEROZYGOSITY FOR ARG506GLN (FACTOR-V-LEIDEN) AND HIS1299ARGSUBSTITUTIONS IN FACTOR-V, British Journal of Haematology, 99(2), 1997, pp. 257-261
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BERNARDI F
FAIONI EM
CASTOLDI E
LUNGHI B
CASTAMAN G
SACCHI E
MANNUCCI PM
Citation: F. Bernardi et al., A FACTOR-V GENETIC COMPONENT DIFFERING FROM FACTOR-V R506Q CONTRIBUTES TO THE ACTIVATED PROTEIN-C RESISTANCE PHENOTYPE, Blood, 90(4), 1997, pp. 1552-1557
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LUNGHI B
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FORMIGLI L
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LEGNANI C
MICHELETTI F
LUNGHI B
FERRARESI P
PALARETI G
BIAGI R
MARCHETTI G
Citation: F. Bernardi et al., A HEPARIN-COFACTOR-II MUTATION (HCII RIMINI) COMBINED WITH FACTOR-V LEIDEN OR TYPE-I PROTEIN-C DEFICIENCY IN 2 UNRELATED THROMBOPHILIC SUBJECTS, Thrombosis and haemostasis, 76(4), 1996, pp. 505-509
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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
Citation: M. Stio et al., EFFECT OF 1,25-DIHYDROXYVITAMIN D-3 ON PROLIFERATION IN SENESCENT IMR-90 HUMAN FIBROBLASTS, Mechanism of ageing and development, 91(1), 1996, pp. 23-36
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FRISO S
MANZATO F
GRAZIOLI S
BERNARDI F
LUNGHI B
GIRELLI D
AZZINI M
BROCCO G
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CORROCHER R
Citation: O. Olivieri et al., RESISTANCE TO ACTIVATED PROTEIN-C, ASSOCIATED WITH ORAL-CONTRACEPTIVES USE EFFECT OF FORMULATIONS, DURATION OF ASSUMPTION, AND DOSES OF OESTRO-PROGESTINS, Contraception, 54(3), 1996, pp. 149-152
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MORATELLI S
BALLERINI G
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LUNGHI B
MARCHETTI G
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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
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COCCHERI S
PALARETI G
LEGNANI C
LUNGHI B
BERNARDI F
SCHENA FP
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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
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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
Authors:
BIAGI R
LEGNANI C
PALARETI G
COCCHERI S
BERNARDI F
LUNGHI B
MARCHETTI G
Citation: R. Biagi et al., COMBINED APC RESISTANCE AND HEPARIN COFACTOR-II DEFICIENCY IN AN ITALIAN FAMILY, Thrombosis and haemostasis, 73(6), 1995, pp. 1369-1369