CASTOLDI, Elisabetta
CASTOLDI, Elisabetta
Dipartimento di Morfologia, chirurgia e medicina sperimentale (attivo dal 01/10/2012 al 31/12/2022)
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
Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family
file con accesso da definire2000 Castoldi, Elisabetta; Simioni, P; Kalafatis, M; Lunghi, Barbara; Tormene, D; Girelli, D; Girolami, A; Bernardi, Francesco
Factor V gene mutations (R2 gene) are associated with coronary artery disease inelderly people
file con accesso da definire1999 Castoldi, Elisabetta; Rosing, J.; Lunghi, Barbara; Hoekema, L.; Girelli, D.; Mingozzi, Federico; Ferraresi, Paolo; Friso, S.; Corrocher, R.; Tans, G.; Bernardi, Francesco
Factor V markers for the detection of genetic components of APC resistance in venous thrombosis
file con accesso da definire1999 Mingozzi, Federico; Lunghi, Barbara; Ferraresi, Paolo; Castoldi, Elisabetta; Legnani, C.; Girelli, D.; Pancani, C.; Palareti, G.; Marchetti, Giovanna; Bernardi, Francesco
FV multiallelic marker detects genetic components of APC resistance contributing to venous thromboembolism in FV Leiden carriers
2003 Mingozzi, F; Legnani, C; Lunghi, B; Scanavini, D; Castoldi, E; Palareti, G; Marchetti, Giovanna; Bernardi, Francesco
Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma
file con accesso da definire2000 Castoldi, Elisabetta; Rosing, J; Girelli, D; Hoekema, L; Lunghi, Barbara; Mingozzi, Federico; Ferraresi, Paolo; Friso, S; Corrocher, R; Tans, G; Bernardi, Francesco
Study of a G/A variation in the 3' untranslated region of prothrombin mRNA in Italian patients with venous thrombosis
file con accesso da definire1997 Ferraresi, Paolo; Legnani, C.; Quaglio, S.; Castoldi, Elisabetta; Marchetti, Giovanna; Palareti, G.; Bernardi, Francesco
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease
file con accesso da definire1997 Ferraresi, Paolo; Marchetti, Giovanna; Legnani, C; Cavallari, Erica; Castoldi, Elisabetta; Mascoli, Francesco; Ardissino, D; Palareti, G; Bernardi, Francesco
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| 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 |
| Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family | 2000 | Castoldi, Elisabetta; Simioni, P; Kalafatis, M; Lunghi, Barbara; Tormene, D; Girelli, D; Girolami..., A; Bernardi, Francesco | file con accesso da definire |
| Factor V gene mutations (R2 gene) are associated with coronary artery disease inelderly people | 1999 | Castoldi, Elisabetta; Rosing, J.; Lunghi, Barbara; Hoekema, L.; Girelli, D.; Mingozzi, Federico; ...Ferraresi, Paolo; Friso, S.; Corrocher, R.; Tans, G.; Bernardi, Francesco | file con accesso da definire |
| Factor V markers for the detection of genetic components of APC resistance in venous thrombosis | 1999 | Mingozzi, Federico; Lunghi, Barbara; Ferraresi, Paolo; Castoldi, Elisabetta; Legnani, C.; Girelli..., D.; Pancani, C.; Palareti, G.; Marchetti, Giovanna; Bernardi, Francesco | file con accesso da definire |
| FV multiallelic marker detects genetic components of APC resistance contributing to venous thromboembolism in FV Leiden carriers | 2003 | Mingozzi, F; Legnani, C; Lunghi, B; Scanavini, D; Castoldi, E; Palareti, G; Marchetti, Giovanna; ...Bernardi, Francesco | |
| Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma | 2000 | Castoldi, Elisabetta; Rosing, J; Girelli, D; Hoekema, L; Lunghi, Barbara; Mingozzi, Federico; Fer...raresi, Paolo; Friso, S; Corrocher, R; Tans, G; Bernardi, Francesco | file con accesso da definire |
| Study of a G/A variation in the 3' untranslated region of prothrombin mRNA in Italian patients with venous thrombosis | 1997 | Ferraresi, Paolo; Legnani, C.; Quaglio, S.; Castoldi, Elisabetta; Marchetti, Giovanna; Palareti, ...G.; Bernardi, Francesco | file con accesso da definire |
| The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease | 1997 | Ferraresi, Paolo; Marchetti, Giovanna; Legnani, C; Cavallari, Erica; Castoldi, Elisabetta; Mascol...i, Francesco; Ardissino, D; Palareti, G; Bernardi, Francesco | file con accesso da definire |