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Mostrati risultati da 17 a 36 di 60
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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
Familial thrombophilia and occurrence of fetal growth restriction. 1-gen-2001 Martinelli, P; Grandone, E; Colaizzo, D; Paladini, D; Sciannamé, N; Margaglione, Maurizio; Di Minno, G.
Familial thrombophilia and the occurrence of fetal growth restriction. Haematologica. 2001, 86(4):428-31 1-gen-2001 Martinelli, P; Grandone, E; Colaizzo, D; Paladini, D; Scianname, N; Margaglione, M; Di Minno, G
Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism. 1-gen-2003 D'Andrea, Giovanna; Margaglione, Maurizio
Homocysteine, plasma function and thrombosis. 1-gen-1999 Di Minno, G; Coppola, A; Mancini, Fp; Margaglione, Maurizio
Human monocyte-derived dendritic cells exposed to hyperthermia show a distinct gene expression profile and selective upregulation of IGFBP-6 1-gen-2014 Liso, A; Massenzio, F; Pucciarini, A; Bigerna, B; De, Luca; Zoppoli, P; Castiglione, F; Conese, M; Castellani, S; Stracci, F; Landriscina, M; Specchia, G); Bach, L; Falini, B.
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
Impact of prothrombotic mutations and family history on the occurrence of intra-uterine fetal deaths. 1-gen-2002 Grandone, E; Colaizzo, D; Brancaccio, V; Ciampa, A; Di Minno, G; Margaglione, Maurizio
. Impact of prothrombotic mutations and family history on the occurrence of intra-uterine fetal deaths. Haematologica 2002; 87(10):1118-9 1-gen-2002 Grandone, E; Colaizzo, D; Brancaccio, V; Ciampa, A; Di Minno, G; Margaglione, M
Inheredited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle piastrine 1-gen-2003 Balduini, C; Cattaneo, M; Fabris, F; Gresele, P; Iolascon, Achille; Pulcinelli, F; Savoia, A.
Inherited thrombophilic risk factors in a large cohort of individuals referred to Italian thrombophilia centers: distinct roles in different clinical settings. Haematologica. 2001; 86(6): 634-9 1-gen-2001 Margaglione, M; Brancaccio, V; Ciampa, A; Papa, Ml; Grandone, E; Di Minno, G
Inherited thrombophilic risk factors in a large cohort of individuals referred to italian thrombophilia centres: distinct role in different clinical settings. 1-gen-2001 Margaglione, Maurizio; Brancaccio, V; Ciampa, A; Papa, Ml; Grandone, E; Di Minno, G.
Intestinal absorption in children with thalassemia major 1-gen-1991 De Mattia, D.; Baldassarre, M. E.; Indrio, F.; Altavilla, T.; Benedetti, G.; De Mitri, D.; Piacente, L.; Cavallo, L.
Lower birth-weight in neonates of mothers carrying factor V G1691A and factor II A(20210) mutations. Haematologica. 2002; 87(2):177-81 1-gen-2002 Grandone, E; Margaglione, M; Colaizzo, D; Pavone, G; Paladini, D; Martinelli, P; Di Minno, G
Lower birth-weight in neonates of mothers carrying factor V G1691A and factor II A(20210) mutations. 1-gen-2002 Grandone, E; Margaglione, Maurizio; Colaizzo, D; Pavone, G; Paladini, D; Martinelli, P; Di Minno, G.
Modulatory effect of mycobacterial heat schock protein 70 in DNA vaccination against lymphoma. Haematologica 1-gen-2005 Liso, Arcangelo; Benedetti, R; Fagioli, M; Mariano, A; Falini, B.
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. Haematologica. 89(8):979-84; 2004 1-gen-2004 D'Andrea, G; Bossone, A; Lupone, Mr; Peyvandi, F; Maisto, G; Perricone, F; Grandone, E; Margaglione, M
Molecular detection of minimal residual disease is associated with early relapse in adult acute lymphoblastic leukemia 1-gen-2004 Specchia, G; Liso, Arcangelo; Pannunzio, A; Albano, F; Mestice, A; Pastore, D; Liso, V.
Multilineage involvement in the 5q- syndrome: a fluorescent in situ hybridization study on bone marrow smears 1-gen-2001 Bigoni, R; Cuneo, A; Milani, R; Cavazzini, F; Bardi, A; Roberti, Mg; Agostini, P; DELLA PORTA, M; Specchia, Giorgina; Rigolin, G. M.; Castoldi, G.
Mostrati risultati da 17 a 36 di 60
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