MARTURANO, ALESSANDRO
MARTURANO, ALESSANDRO
DIPARTIMENTO DI INGEGNERIA
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A novel variant Glanzmann thrombasthenia due to co-inheritance of a loss- and a gain-of-function mutation of ITGB3: evidence of a dominant effect of gain-of-function mutations.
2018 Bury, L; Zetterberg, E; Leinoe, Eb; Falcinelli, E; Marturano, A; Manni, G; Nurden, At; Gresele, P
Platelet and endothelial activation in catastrophic and quiescent antiphospholipid syndrome.
2013 Bontadi, A; Ruffatti, A; Falcinelli, Emanuela; Giannini, Silvia; Marturano, Alessandro; Tonello, M; Hoxha, A; Pengo, V; Punzi, L; Momi, Stefania; Gresele, Paolo
Possible incorrect genotyping of heterozygous factor V Leiden and Prothrombin 20210 gene mutations by the GeneXpert assay.
2014 Marturano, Alessandro; Bury, Loredana; Gresele, Paolo
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A novel variant Glanzmann thrombasthenia due to co-inheritance of a loss- and a gain-of-function mutation of ITGB3: evidence of a dominant effect of gain-of-function mutations. | 2018 | Bury, L; Zetterberg, E; Leinoe, Eb; Falcinelli, E; Marturano, A; Manni, G; Nurden, At; Gresele, P | |
| Platelet and endothelial activation in catastrophic and quiescent antiphospholipid syndrome. | 2013 | Bontadi, A; Ruffatti, A; Falcinelli, Emanuela; Giannini, Silvia; Marturano, Alessandro; Tonello, M; Hoxha, A; Pengo, V; Punzi, L; Momi, Stefania; Gresele, Paolo | |
| Possible incorrect genotyping of heterozygous factor V Leiden and Prothrombin 20210 gene mutations by the GeneXpert assay. | 2014 | Marturano, Alessandro; Bury, Loredana; Gresele, Paolo |