Use of Catridecacog in a patient with severe Factor XIII deficiency undergoing surgery

بواسطة Sottilotta, Gianluca, Luise, Francesca, Oriana, Vincenzo, Piromalli, Angela, Santacroce, Rosa, Di Lelio, Alessandra
الحاوية / القاعدة Hematol Rep (2019)

The Genetics of Hereditary Angioedema: A Review

بواسطة Santacroce, Rosa, D’Andrea, Giovanna, Maffione, Angela Bruna, Margaglione, Maurizio, d’Apolito, Maria
الحاوية / القاعدة J Clin Med (2021)

Prospective evaluation of pregnancy outcome in an Italian woman with late-onset combined homocystinuria and methylmalonic aciduria

بواسطة Grandone, Elvira, Martinelli, Pasquale, Villani, Michela, Vecchione, Gennaro, Fischetti, Lucia, Leccese, Angelica, Santacroce, Rosa, Corso, Gaetano, Margaglione, Maurizio
الحاوية / القاعدة BMC Pregnancy Childbirth (2019)

Severe bleeding and absent ADP-induced platelet aggregation associated with inherited combined CalDAG-GEFI and P2Y(12) deficiencies

بواسطة Lunghi, Barbara, Lecchi, Anna, Santacroce, Rosa, Scavone, Mariangela, Paniccia, Rita, Artoni, Andrea, Gachet, Christian, Castaman, Giancarlo, Margaglione, Maurizio, Bernardi, Francesco, Cattaneo, Marco
الحاوية / القاعدة Haematologica (2020)

Towards the genetic basis of cerebral venous thrombosis—the BEAST Consortium: a study protocol

بواسطة Cotlarciuc, Ioana, Marjot, Thomas, Khan, Muhammad S, Hiltunen, Sini, Haapaniemi, Elena, Metso, Tiina M, Putaala, Jukka, Zuurbier, Susanna M, Brouwer, Matthijs C, Passamonti, Serena M, Bucciarelli, Paolo, Pappalardo, Emanuela, Patel, Tasmin, Costa, Paolo, Colombi, Marina, Canhão, Patrícia, Tkach, Aleksander, Santacroce, Rosa, Margaglione, Maurizio, Favuzzi, Giovanni, Grandone, Elvira, Colaizzo, Donatella, Spengos, Kostas, Arauz, Antonio, Hodge, Amanda, Ditta, Reina, Debette, Stephanie, Zedde, Marialuisa, Pare, Guillaume, Ferro, José M, Thijs, Vincent, Pezzini, Alessandro, Majersik, Jennifer J, Martinelli, Ida, Coutinho, Jonathan M, Tatlisumak, Turgut, Sharma, Pankaj
الحاوية / القاعدة BMJ Open (2016)