LUNGHI, Barbara
LUNGHI, Barbara
Dipartimento di Scienze della vita e biotecnologie
A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype
file con accesso da definire1997 Bernardi, Francesco; Faioni, Em; Castoldi, E; Lunghi, Barbara; Castaman, G; Sacchi, E; Mannucci, Pm
A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjects
file con accesso da definire1996 Bernardi, Francesco; Legnani, C; Micheletti, Fabiola; Lunghi, Barbara; Ferraresi, Paolo; Palareti, G; Biagi, R; Marchetti, Giovanna
A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disorders
file con accesso da definire2001 Castoldi, Elisabetta; Lunghi, Barbara; Mingozzi, Federico; Simioni, P; Girolami, A; Bernardi, Francesco
A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the Italian population.
file con accesso da definire2001 Castoldi, Elisabetta; Lunghi, Barbara; Mingozzi, Federico; Muleo, G; Redaelli, R; Mariani, G; Bernardi, Francesco
A new factor V gene polymorphism (His 1254 Arg) present in subjects of African origin mimics the R2 polymorphism (His 1299 Arg)
file con accesso da definire1998 Lunghi, Barbara; Castoldi, E; Mingozzi, F; Bernardi, Francesco
A novel factor V null mutation detected in a thrombophilic patient with pseudo-homozygous APC resistance and in an asymptomatic unrelated subject
file con accesso da definire1998 Lunghi, Barbara; Castoldi, E; Mingozzi, F; Bernardi, Francesco; Castaman, G.
A novel mutation (Leu817Pro) causing type 2A von Willebrand disease.
file con accesso da definire1996 Gemmati, Donato; Serino, Maria Luisa; Moratelli, S.; Ballerini, G.; Furbetta, M.; Lunghi, Barbara; Marchetti, Giovanna; Bernardi, Francesco
Activated factor VII-antithrombin complex predicts mortality in patients with stable coronary artery disease: a cohort study
2016 Martinelli, N; Girelli, D; Baroni, Marcello; Guarini, P; Sandri, M; Lunghi, Barbara; Tosi, F; Branchini, Alessio; Sartori, F; Woodhams, B; Bernardi, Francesco; Olivieri, O.
An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis
2015 Marchetti, Giovanna; Girelli, D; Zerbinati, Carlotta; Lunghi, Barbara; Friso, S; Meneghetti, Silvia; Coen, Matteo; Gagliano, Teresa; Guastella, Giuseppe; Bochaton Piallat, Ml; Pizzolo, F; Mascoli, Francesco; Malerba, G; Bovolenta, Matteo; Ferracin, Manuela; Olivieri, O; Bernardi, Francesco; Martinelli, N.
An Italian Family with a Novel Mutation Causing Type 2A von Willebrand Disease and with Reduced Levels of von Willebrand Factor not Linked with the von Willebrand Factor Gene.
file con accesso da definire1995 Gemmati, Donato; Serino, Maria Luisa; Moratelli, S.; Ballerini, G.; Furbetta, M.; Lunghi, Barbara; Marchetti, Giovanna; Bernardi, Francesco
An underestimated combination of opposites resulting in enhanced thrombotic tendency
file con accesso da definire2005 Simioni, P; Castoldi, E; Lunghi, Barbara; Tormene, D; Rosing, J; Bernardi, Francesco
Apolipoprotein C-III Strongly Correlates with Activated Factor VII-Anti-Thrombin Complex: An Additional Link between Plasma Lipids and Coagulation
2019 Martinelli, N; Baroni, M; Castagna, A; Lunghi, B; Stefanoni, F; Tosi, F; Croce, J; Udali, S; Woodhams, B; Girelli, D; Bernardi, F; Olivieri, O
Aptamer-modified FXa generation assays to investigate hypercoagulability in plasma from patients with ischemic heart disease
2020 Baroni, Marcello; Martinelli, Nicola; Lunghi, Barbara; Marchetti, Giovanna; Castagna, Annalisa; Stefanoni, Filippo; Pinotti, Mirko; Woodhams, Barry; Olivieri, Oliviero; Bernardi, Francesco
Association of membranous nephropathy with familial resistance to activated protein C
file con accesso da definire1995 Montinaro, V; Coccheri, S; Palareti, G; Legnani, C; Lunghi, Barbara; Bernardi, F; Schena, Fp
Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster
file con accesso da definire2003 Marchetti, Giovanna; Ferraresi, Paolo; Legnani, C; Pinotti, Mirko; Lunghi, Barbara; Scapoli, Chiara; Gemmati, Donato; Coccheri, S; Palareti, G; Bernardi, Francesco
C6orf10 low-frequency and rare variants in italian multiple sclerosis patients
2019 Ziliotto, Nicole; Marchetti, Giovanna; Scapoli, Chiara; Bovolenta, Matteo; Meneghetti, Silvia; Benazzo, Andrea; Lunghi, Barbara; Balestra, Dario; Laino, Lorenza Anna; Bozzini, Nicolò; Guidi, Irene; Salvi, Fabrizio; Straudi, Sofia; Gemmati, Donato; Menegatti, Erica; Zamboni, Paolo; Bernardi, Francesco
Changes in expression profiles of internal jugular vein wall and plasma protein levels in multiple sclerosis
2018 Marchetti, G; Ziliotto, N; Meneghetti, Silvia; Baroni, M; Lunghi, B; Menegatti, E; Pedriali, M; Salvi, F; Bartolomei, I; Straudi, Sofia; Manfredini, F; Voltan, R; Basaglia, N; Mascoli, F; Zamboni, P; Bernardi, F.
Cis-segregation of c.1171c>t stop codon (p.r391*) in serpinc1 gene and c.1691g>a transition (p.r506q) in f5 gene and selected gwas multilocus approach in inherited thrombophilia
2021 Gemmati, D.; Longo, G.; Franchini, E.; Silva, J. A.; Gallo, I.; Lunghi, B.; Moratelli, S.; Maestri, I.; Serino, M. L.; Tisato, V.
CMR+ Factor V deficiency Arg2080Cys: A model to investigate altered C2 domain-membrane interaction.
file con accesso da definire2005 Scanavini, D; Lunghi, Barbara; Gemmati, Donato; Canella, A; Grandini, A; Tognazzo, S; Bernardi, Francesco
Combination of CLEC4M rs868875 G-Carriership and ABO O Genotypes May Predict Faster Decay of FVIII Infused in Hemophilia A Patients
2022 Lunghi, B.; Morfini, M.; Martinelli, N.; Linari, S.; Castaman, G.; Bernardi, F.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype | 1997 | Bernardi, Francesco; Faioni, Em; Castoldi, E; Lunghi, Barbara; Castaman, G; Sacchi, E; Mannucci, Pm | file con accesso da definire |
| A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjects | 1996 | Bernardi, Francesco; Legnani, C; Micheletti, Fabiola; Lunghi, Barbara; Ferraresi, Paolo; Palareti..., G; Biagi, R; Marchetti, Giovanna | file con accesso da definire |
| A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disorders | 2001 | Castoldi, Elisabetta; Lunghi, Barbara; Mingozzi, Federico; Simioni, P; Girolami, A; Bernardi, Fra...ncesco | file con accesso da definire |
| A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the Italian population. | 2001 | Castoldi, Elisabetta; Lunghi, Barbara; Mingozzi, Federico; Muleo, G; Redaelli, R; Mariani, G; Ber...nardi, Francesco | file con accesso da definire |
| A new factor V gene polymorphism (His 1254 Arg) present in subjects of African origin mimics the R2 polymorphism (His 1299 Arg) | 1998 | Lunghi, Barbara; Castoldi, E; Mingozzi, F; Bernardi, Francesco | file con accesso da definire |
| A novel factor V null mutation detected in a thrombophilic patient with pseudo-homozygous APC resistance and in an asymptomatic unrelated subject | 1998 | Lunghi, Barbara; Castoldi, E; Mingozzi, F; Bernardi, Francesco; Castaman, G. | file con accesso da definire |
| A novel mutation (Leu817Pro) causing type 2A von Willebrand disease. | 1996 | Gemmati, Donato; Serino, Maria Luisa; Moratelli, S.; Ballerini, G.; Furbetta, M.; Lunghi, Barbara...; Marchetti, Giovanna; Bernardi, Francesco | file con accesso da definire |
| Activated factor VII-antithrombin complex predicts mortality in patients with stable coronary artery disease: a cohort study | 2016 | Martinelli, N; Girelli, D; Baroni, Marcello; Guarini, P; Sandri, M; Lunghi, Barbara; Tosi, F; Bra...nchini, Alessio; Sartori, F; Woodhams, B; Bernardi, Francesco; Olivieri, O. | |
| An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis | 2015 | Marchetti, Giovanna; Girelli, D; Zerbinati, Carlotta; Lunghi, Barbara; Friso, S; Meneghetti, Silv...ia; Coen, Matteo; Gagliano, Teresa; Guastella, Giuseppe; Bochaton Piallat, Ml; Pizzolo, F; Mascoli, Francesco; Malerba, G; Bovolenta, Matteo; Ferracin, Manuela; Olivieri, O; Bernardi, Francesco; Martinelli, N. | |
| An Italian Family with a Novel Mutation Causing Type 2A von Willebrand Disease and with Reduced Levels of von Willebrand Factor not Linked with the von Willebrand Factor Gene. | 1995 | Gemmati, Donato; Serino, Maria Luisa; Moratelli, S.; Ballerini, G.; Furbetta, M.; Lunghi, Barbara...; Marchetti, Giovanna; Bernardi, Francesco | file con accesso da definire |
| An underestimated combination of opposites resulting in enhanced thrombotic tendency | 2005 | Simioni, P; Castoldi, E; Lunghi, Barbara; Tormene, D; Rosing, J; Bernardi, Francesco | file con accesso da definire |
| Apolipoprotein C-III Strongly Correlates with Activated Factor VII-Anti-Thrombin Complex: An Additional Link between Plasma Lipids and Coagulation | 2019 | Martinelli, N; Baroni, M; Castagna, A; Lunghi, B; Stefanoni, F; Tosi, F; Croce, J; Udali, S; Wood...hams, B; Girelli, D; Bernardi, F; Olivieri, O | |
| Aptamer-modified FXa generation assays to investigate hypercoagulability in plasma from patients with ischemic heart disease | 2020 | Baroni, Marcello; Martinelli, Nicola; Lunghi, Barbara; Marchetti, Giovanna; Castagna, Annalisa; S...tefanoni, Filippo; Pinotti, Mirko; Woodhams, Barry; Olivieri, Oliviero; Bernardi, Francesco | |
| Association of membranous nephropathy with familial resistance to activated protein C | 1995 | Montinaro, V; Coccheri, S; Palareti, G; Legnani, C; Lunghi, Barbara; Bernardi, F; Schena, Fp | file con accesso da definire |
| Asymptomatic carriership of factor V Leiden and genotypes of the fibrinogen gene cluster | 2003 | Marchetti, Giovanna; Ferraresi, Paolo; Legnani, C; Pinotti, Mirko; Lunghi, Barbara; Scapoli, Chia...ra; Gemmati, Donato; Coccheri, S; Palareti, G; Bernardi, Francesco | file con accesso da definire |
| C6orf10 low-frequency and rare variants in italian multiple sclerosis patients | 2019 | Ziliotto, Nicole; Marchetti, Giovanna; Scapoli, Chiara; Bovolenta, Matteo; Meneghetti, Silvia; Be...nazzo, Andrea; Lunghi, Barbara; Balestra, Dario; Laino, Lorenza Anna; Bozzini, Nicolò; Guidi, Irene; Salvi, Fabrizio; Straudi, Sofia; Gemmati, Donato; Menegatti, Erica; Zamboni, Paolo; Bernardi, Francesco | |
| Changes in expression profiles of internal jugular vein wall and plasma protein levels in multiple sclerosis | 2018 | Marchetti, G; Ziliotto, N; Meneghetti, Silvia; Baroni, M; Lunghi, B; Menegatti, E; Pedriali, M; S...alvi, F; Bartolomei, I; Straudi, Sofia; Manfredini, F; Voltan, R; Basaglia, N; Mascoli, F; Zamboni, P; Bernardi, F. | |
| Cis-segregation of c.1171c>t stop codon (p.r391*) in serpinc1 gene and c.1691g>a transition (p.r506q) in f5 gene and selected gwas multilocus approach in inherited thrombophilia | 2021 | Gemmati, D.; Longo, G.; Franchini, E.; Silva, J. A.; Gallo, I.; Lunghi, B.; Moratelli, S.; Maestr...i, I.; Serino, M. L.; Tisato, V. | |
| CMR+ Factor V deficiency Arg2080Cys: A model to investigate altered C2 domain-membrane interaction. | 2005 | Scanavini, D; Lunghi, Barbara; Gemmati, Donato; Canella, A; Grandini, A; Tognazzo, S; Bernardi, F...rancesco | file con accesso da definire |
| Combination of CLEC4M rs868875 G-Carriership and ABO O Genotypes May Predict Faster Decay of FVIII Infused in Hemophilia A Patients | 2022 | Lunghi, B.; Morfini, M.; Martinelli, N.; Linari, S.; Castaman, G.; Bernardi, F. |