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Mostrati risultati da 1 a 5 di 5
SDF1-3'A gene polymorphism is associated with chronic myeloproliferative disease and thrombotic events
2005 G. Gerli, C. Vanelli, O. Turri, M. Erario, A. Gardellini, M. Pugliano, M.L. Biondi
Plasma homocysteine and oxydative stress in polycythemia vera and essential thrombocythemia. Effect of folic acid supplementation
2005 M. Pugliano, M.L. Biondi, C. Vanelli, A. Gardellini, L. Battaglioli, M. Erario, A. La Torre, O. Turri, C. Maioli, G. Gerli
Endothelial nitric oxide synthase gene polymorphisms (G894T and T786C) in essential throbocythemia
2005 A. Gardellini, M.L. Biondi, O. Turri, M. Pugliano, C. Vanelli, L. Battaglioli, M. Erario, A. La Torre, G. Gerli
SDF1-3'A gene polymorphism : risk factor for thrombotic events in Philadelphia-negative chronic myeloproliferative disorders
2005 C. Vanelli, M.L. Biondi, O. Turri, A. La Torre, A. Gardellini, M. Pugliano, L. Battaglioli, M. Erario, G. Gerli
Cerebral microbleeds : A new presenting feature of chromosome 22q11.2 deletion syndrome
2016 M.T. Bonati, C. Vanelli, D. Sangalli, C. Sina, D. Giardino, J. Sassone, F. Girotti, V. Silani, A. Ciammola
Titolo | Data di pubblicazione | Autori | Tipo | File | Abstract |
---|---|---|---|---|---|
SDF1-3'A gene polymorphism is associated with chronic myeloproliferative disease and thrombotic events | 2005 | G. GerliC. VanelliA. GardelliniM. Pugliano + | Article (author) | - | |
Plasma homocysteine and oxydative stress in polycythemia vera and essential thrombocythemia. Effect of folic acid supplementation | 2005 | M. PuglianoC. VanelliA. GardelliniC. MaioliG. Gerli + | Article (author) | - | |
Endothelial nitric oxide synthase gene polymorphisms (G894T and T786C) in essential throbocythemia | 2005 | A. GardelliniM. PuglianoC. VanelliG. Gerli + | Article (author) | - | |
SDF1-3'A gene polymorphism : risk factor for thrombotic events in Philadelphia-negative chronic myeloproliferative disorders | 2005 | C. VanelliA. GardelliniM. PuglianoG. Gerli + | Article (author) | - | |
Cerebral microbleeds : A new presenting feature of chromosome 22q11.2 deletion syndrome | 2016 | VANELLI, CHIARASANGALLI, DAVIDEV. Silani + | Article (author) | - |
Mostrati risultati da 1 a 5 di 5
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