Sfoglia per Autore  

Opzioni
Mostrati risultati da 21 a 40 di 117
Titolo Data di pubblicazione Autore(i) File
High prevalence of thrombophilic genotypes in patients with acute mesenteric vein thrombosis. 1-gen-2001 Amitrano, L; Brancaccio, V; Guardascione, Ma; Margaglione, Maurizio; Iannaccone, L; D'Andrea, Giovanna; Ames, Pr; Marmo, R; Mosca, S; Balzano, A.
RGD-containing peptides inhibit fibrinogen binding to platelet alpha(IIb)beta3 by inducing an allosteric change in the amino-terminal portion of alpha(IIb). 1-gen-2001 Basani, Rb; D'Andrea, Giovanna; Mitra, N; Vilaire, G; Richberg, M; Kowalska, Ma; Bennett, Js; Poncz, M.
Glanzmann's thrombasthenia: identification of 19 new mutations in 30 patients 1-gen-2002 D'Andrea, Giovanna; Colaizzo, D.; Vecchione, G.; Grandone, E.; DI MINNO, G.; Margaglione, Maurizio
FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile 1-gen-2002 Margaglione, Maurizio; Bossone, A.; Coalizzo, D.; D'Andrea, Giovanna; Brancaccio, V.; Ciampa, A.; Grandone, E.; DI MINNO, G.
. FV HR2 haplotype as additional inherited risk factor for deep vein thrombosis in individuals with a high-risk profile. Thromb Haemost. 2002; 87(1):32-6. 1-gen-2002 Margaglione, M; Bossone, A; Colaizzo, D; D'Andrea, G; Brancaccio, V; Ciampa, A; Grandone, E; Di Minno, G
The factor V (FV) gene ASP79HIS polymorphism modulates FV plasma levels and affects the activated protein C resistance phenotype in presence of the FV Leiden mutation 1-gen-2003 Bossone, A.; Cappucci, F.; D'Andrea, Giovanna; Brancaccio, V.; Cibelli, Giuseppe; Iannaccone, L.; Grandone, E.; Margaglione, Maurizio
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 1-gen-2003 D'Andrea, Giovanna; Margaglione, Maurizio
. The factor V (FV) gene ASP79HIS polymorphism modulates FV plasma levels and affects the activated protein C resistance phenotype in presence of the FV Leiden mutation. Haematologica 2003; .88(3):286-9. 1-gen-2003 Bossone, A; Cappucci, F; D'Andrea, G; Brancaccio, V; Cibelli, G; Iannaccone, L; Grandone, E; Margaglione, M
A novel G-to-A mutation in the intron-N of the protein S gene leading to abnormal RNA splicing in a patient with protein S deficiency. 1-gen-2003 D'Andrea, Giovanna; DI PERNA, P.; Brancaccio, V.; Faioni, E. M.; Castaman, G.; Cibelli, Giuseppe; DI MINNO, G.; Margaglione, Maurizio
Molecular characterization of a factor Vii deficient patient supports the importance of the second epidermal growth factor-like domain. 1-gen-2004 D'Andrea, Giovanna; Bossone, A; Lupone, Mr; Peyvandi, F; Maisto, G; Perricone, F; Grandone, E; Margaglione, Maurizio
Molecular characterization of a factor VII deficient patient supports the importance of the second epidermal growth factor-like domain. 1-gen-2004 D'Andrea, G; Bossone, A; Lupone, Mr; Peyvandi, F; Maisto, G; Perricone, F; Grandone, E; Margaglione, Maurizio
Identification of six novel mutations in type I antithrombin deficient Italian families 1-gen-2004 DI PERNA, P; Vecchione, G; D'Andrea, Giovanna; Scenna, G; Brancaccio, V; Margaglione, Maurizio
Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin 1-gen-2004 D'Ambrosio, R. L.; D'Andrea, Giovanna; Cappucci, F.; Chetta, M.; DI PERNA, P.; Brancaccio, V.; Grandone, E.; Margaglione, Maurizio
. Polymorphisms in factor II and factor VII genes modulate oral anticoagulation with warfarin. Haematologica 2004; 89(12):1510-6. 1-gen-2004 D'Ambrosio, Rl; D'Andrea, G; Cappucci, F; Chetta, M; Di Perna, P; Brancaccio, V; Grandone, E; Margaglione, M
Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study. 1-gen-2005 Biguzzi, E; Razzari, C; Lane, Da; Castaman, G; Cappellari, A; Bucciarelli, P; Fontana, G; Margaglione, Maurizio; D'Andrea, Giovanna; Simmonds, Re; Rezende, Sm; Preston, R; Prisco, D; Faioni, Em; PROTEIN S., ITALIAN TEAM
A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin 1-gen-2005 D'Andrea, Giovanna; D'Ambrosio, Rl; Di Perna, P; Chetta, Massimiliano; Santacroce, Rosa; Brancaccio, V; Grandone, E; Margaglione, Maurizio
A polymorfism in VKORC1 gene is associated with an interindividual variability in the dose-anticoagulation effect of warfarin. 1-gen-2005 D'Andrea, Giovanna; Dambrosio, R. L.; P, DI ERNA .; Chetta, M.; Santacroce, Rosa; Brancaccio, V.; Grandone, E.; Margaglione, Maurizio
.A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin. Blood. 105(2):645-9; 2005 1-gen-2005 D'Andrea, G; D'Ambrosio, Rl; Di Perna, P; Chetta, M; Santacroce, R; Brancaccio, V; Grandone, E; Margaglione, M
Role of tumour necrosis factor alpha and interleukin 1 beta in promoter effect induced by mercury in human keratinocytes 1-gen-2006 Zefferino, Roberto; Piccaluga, S.; Lasalvia, M.; D'Andrea, Giovanna; Margaglione, Maurizio; Ambrosi, Luigi
A new vitamin K epoxide reductase complex subunit-1 (VKORC1) mutation in a patient with decreased stability of CYP2C9 enzyme 1-gen-2007 D'Ambrosio, R. L.; D'Andrea, Giovanna; Cafolla, A.; Faillace, F.; Margaglione, Maurizio
Mostrati risultati da 21 a 40 di 117
Legenda icone

  •  file ad accesso aperto
  •  file disponibili sulla rete interna
  •  file disponibili agli utenti autorizzati
  •  file disponibili solo agli amministratori
  •  file sotto embargo
  •  nessun file disponibile