Sfoglia per Rivista HAEMOPHILIA
Clinical histories and molecular characterization of two afibrinogenemic patients: insights into clinical management. Haemophilia. 2012 Jan;18(1):e16-8
2012-01-01 Grandone, E; Tiscia, G; Cappucci, F; Favuzzi, G; Santacroce, R; Pisanelli, D; Soli, F; Legnani, C; Rizzo, Ma; Palareti, G; Margaglione, M
Clinical histories and molecular characterization of two afibrinogenemic patients: insights into clinical management.
2012-01-01 Grandone, E; Tiscia, G; Cappucci, F; Favuzzi, G; Santacroce, Rosa; Pisanelli, D; Soli, F; Legnani, C; Rizzo, Ma; Palareti, G; Margaglione, Maurizio
Coinheritance of three novel FV gene mutations in a patient with a severe FV deficiency.
2012-01-01 Bafunno, V; Favuzzi, G; Fierro, T; Chetta, M; Mastrodicasa, E; Chinni, E; Grandone, E; Margaglione, Maurizio; Gresele, P.
Factor XI deficiency: two novel mutations in asymptomatic Italian patients.
2010-01-01 Tomaiuolo, M; Favuzzi, G; Cappucci, F; Pisanelli, D; Tiscia, Gl; Musto, P; Scaraggi, Fa; Cincione, RAFFAELE IVAN; Margaglione, Maurizio; Grandone, E.
Factor XI deficiency: two novelmutations in asymptomatic Italian patients
2010-01-01 Tomaiuolo, M; Favuzzi, G; Cappucci, F; Pisanelli, D; Tiscia, Gl; Musto, P; Scaraggi, Fa; Cincione, Ri; Margaglione, M; Grandone, E
FXI deficiency: two novel mutations in asymptomatic Italian patients
2010-01-01 Tomaiuolo, M.; Favuzzi, G.; Cappucci, F.; Pisanelli, D.; Tiscia, G.; Musto, P.; Scaraggi, F.; Cincione, RAFFAELE IVAN; Margaglione, Maurizio; Grandone, E.
IDEAL study: A real-world assessment of pattern of use and clinical outcomes with recombinant coagulation factor IX albumin fusion protein (rIX-FP) in patients with haemophilia B in Italy
2023-01-01 Tagliaferri, Annarita; Molinari, Angelo Claudio; Peyvandi, Flora; Coppola, Antonio; Demartis, Francesco; Biasoli, Chiara; Borchiellini, Alessandra; Cultrera, Dorina; De Cristofaro, Raimondo; Daniele, Filomena; Giordano, Paola; Marchesini, Emanuela; Margaglione, Maurizio; Marino, Renato; Pollio, Berardino; Radossi, Paolo; Santoro, Cristina; Santoro, Rita Carlotta; Siragusa, Sergio; Sottilotta, Gianluca; Tosetto, Alberto; Piscitelli, Lydia; Villa, Maria Rosaria; Zanon, Ezio; Finardi, Adele; Schiavetti, Irene; Vaccari, Daniella; Castaman, Giancarlo
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia
2006-01-01 Santacroce, Rosa; Vecchione, G; Tomaiuolo, M; Sessa, F; Sarno, M; Colaizzo, D; Grandone, E; Margaglione, Maurizio
. Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia. Haemophilia. 2006 ;12(4):417-22
2006-01-01 Santacroce, R; Vecchione, G; Tomaiuolo, M; Sessa, F; Sarno, M; Colaizzo, D; Grandone, E; Margaglione, M
Management of patients with factor V deficiency: open issues from the challenging history of a woman with anaphylactic transfusion reactions.
2010-01-01 Coppola, A; Maruotti, Gm; Feola, G; Catalano, A; Quaglia, F; Tomaiuolo, M; DI MINNO, Mn; Cerbone, Am; Margaglione, Maurizio; Martinelli, P.
Polymorphic miRNA-mediated gene contribution to inhibitor development in haemophilia A
2012-01-01 Bafunno, V; Santacroce, Rosa; Chetta, M; Peyvandi, F; Sessa, Francesco; Chinni, E; Longo, V; Margaglione, Maurizio
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A
2010-01-01 Bafunno, V.; Santacroce, R.; Chetta, M.; D'Andrea, G.; Pisanelli, D.; Sessa, F.; Trotta, T.; Tagariello, G.; Peyvandi, F.; Margaglione, M.
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A
2010-01-01 Bafunno, V.; Santacroce, Rosa; Chetta, M.; D'Andrea, Giovanna; Pisanelli, D.; Sessa, F.; Trotta, Teresa; Tagariello, G.; Peyvandi, F.; Margaglione, Maurizio
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A.
2009-01-01 Bafunno, V; Santacroce, Rosa; Chetta, M; D'Andrea, Giovanna; Pisanelli, D; Sessa, F; Trotta, Teresa; Tagariello, G; Peyvandi, F; Margaglione, Maurizio
Predictors of inhibitor eradication by primary immune tolerance induction in severe haemophilia A with high responding inhibitors
2022-01-01 Di Minno, G; Coppola, A; Margaglione, M; Rocino, A; Mancuso, Me; Tagliaferri, A; Linari, S; Zanon, E; Santoro, C; Biasoli, C; Castaman, G; Santagostino, E; Mannucci, Pm
Prenatal diagnosis of haemophilia B: the Italian experience.
2013-01-01 Belvini, D; Salviato, R; Acquila, M; Bicocchi, Mp; Frusconi, S; Garagiola, I; Sanna, V; Santacroce, Rosa; Rocino, A; Tagariello, G.
Venous thrombosis in afibrinogenemia: a successful use of rivaroxaban.
2015-01-01 Margaglione, M; Vecchione, G; Cappucci, F; Macarini, L; D'Andrea, G; Di Matteo, C; Grandone, E
Venous thrombosis in afibrinogenemia: a successful use of rivaroxaban
2015-01-01 Margaglione, Maurizio; Vecchione, G; Cappucci, F; Macarini, Luca; D'Andrea, Giovanna; Di Matteo, C; Grandone, E.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Clinical histories and molecular characterization of two afibrinogenemic patients: insights into clinical management. Haemophilia. 2012 Jan;18(1):e16-8 | 1-gen-2012 | Grandone, E; Tiscia, G; Cappucci, F; Favuzzi, G; Santacroce, R; Pisanelli, D; Soli, F; Legnani, C; Rizzo, Ma; Palareti, G; Margaglione, M | |
Clinical histories and molecular characterization of two afibrinogenemic patients: insights into clinical management. | 1-gen-2012 | Grandone, E; Tiscia, G; Cappucci, F; Favuzzi, G; Santacroce, Rosa; Pisanelli, D; Soli, F; Legnani, C; Rizzo, Ma; Palareti, G; Margaglione, Maurizio | |
Coinheritance of three novel FV gene mutations in a patient with a severe FV deficiency. | 1-gen-2012 | Bafunno, V; Favuzzi, G; Fierro, T; Chetta, M; Mastrodicasa, E; Chinni, E; Grandone, E; Margaglione, Maurizio; Gresele, P. | |
Factor XI deficiency: two novel mutations in asymptomatic Italian patients. | 1-gen-2010 | Tomaiuolo, M; Favuzzi, G; Cappucci, F; Pisanelli, D; Tiscia, Gl; Musto, P; Scaraggi, Fa; Cincione, RAFFAELE IVAN; Margaglione, Maurizio; Grandone, E. | |
Factor XI deficiency: two novelmutations in asymptomatic Italian patients | 1-gen-2010 | Tomaiuolo, M; Favuzzi, G; Cappucci, F; Pisanelli, D; Tiscia, Gl; Musto, P; Scaraggi, Fa; Cincione, Ri; Margaglione, M; Grandone, E | |
FXI deficiency: two novel mutations in asymptomatic Italian patients | 1-gen-2010 | Tomaiuolo, M.; Favuzzi, G.; Cappucci, F.; Pisanelli, D.; Tiscia, G.; Musto, P.; Scaraggi, F.; Cincione, RAFFAELE IVAN; Margaglione, Maurizio; Grandone, E. | |
IDEAL study: A real-world assessment of pattern of use and clinical outcomes with recombinant coagulation factor IX albumin fusion protein (rIX-FP) in patients with haemophilia B in Italy | 1-gen-2023 | Tagliaferri, Annarita; Molinari, Angelo Claudio; Peyvandi, Flora; Coppola, Antonio; Demartis, Francesco; Biasoli, Chiara; Borchiellini, Alessandra; Cultrera, Dorina; De Cristofaro, Raimondo; Daniele, Filomena; Giordano, Paola; Marchesini, Emanuela; Margaglione, Maurizio; Marino, Renato; Pollio, Berardino; Radossi, Paolo; Santoro, Cristina; Santoro, Rita Carlotta; Siragusa, Sergio; Sottilotta, Gianluca; Tosetto, Alberto; Piscitelli, Lydia; Villa, Maria Rosaria; Zanon, Ezio; Finardi, Adele; Schiavetti, Irene; Vaccari, Daniella; Castaman, Giancarlo | |
Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia | 1-gen-2006 | Santacroce, Rosa; Vecchione, G; Tomaiuolo, M; Sessa, F; Sarno, M; Colaizzo, D; Grandone, E; Margaglione, Maurizio | |
. Identification of fetal gender in maternal blood is a helpful tool in the prenatal diagnosis of haemophilia. Haemophilia. 2006 ;12(4):417-22 | 1-gen-2006 | Santacroce, R; Vecchione, G; Tomaiuolo, M; Sessa, F; Sarno, M; Colaizzo, D; Grandone, E; Margaglione, M | |
Management of patients with factor V deficiency: open issues from the challenging history of a woman with anaphylactic transfusion reactions. | 1-gen-2010 | Coppola, A; Maruotti, Gm; Feola, G; Catalano, A; Quaglia, F; Tomaiuolo, M; DI MINNO, Mn; Cerbone, Am; Margaglione, Maurizio; Martinelli, P. | |
Polymorphic miRNA-mediated gene contribution to inhibitor development in haemophilia A | 1-gen-2012 | Bafunno, V; Santacroce, Rosa; Chetta, M; Peyvandi, F; Sessa, Francesco; Chinni, E; Longo, V; Margaglione, Maurizio | |
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A | 1-gen-2010 | Bafunno, V.; Santacroce, R.; Chetta, M.; D'Andrea, G.; Pisanelli, D.; Sessa, F.; Trotta, T.; Tagariello, G.; Peyvandi, F.; Margaglione, M. | |
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A | 1-gen-2010 | Bafunno, V.; Santacroce, Rosa; Chetta, M.; D'Andrea, Giovanna; Pisanelli, D.; Sessa, F.; Trotta, Teresa; Tagariello, G.; Peyvandi, F.; Margaglione, Maurizio | |
Polymorphisms in genes involved in autoimmune disease and the risk of FVIII inhibitor development in Italian patients with haemophilia A. | 1-gen-2009 | Bafunno, V; Santacroce, Rosa; Chetta, M; D'Andrea, Giovanna; Pisanelli, D; Sessa, F; Trotta, Teresa; Tagariello, G; Peyvandi, F; Margaglione, Maurizio | |
Predictors of inhibitor eradication by primary immune tolerance induction in severe haemophilia A with high responding inhibitors | 1-gen-2022 | Di Minno, G; Coppola, A; Margaglione, M; Rocino, A; Mancuso, Me; Tagliaferri, A; Linari, S; Zanon, E; Santoro, C; Biasoli, C; Castaman, G; Santagostino, E; Mannucci, Pm | |
Prenatal diagnosis of haemophilia B: the Italian experience. | 1-gen-2013 | Belvini, D; Salviato, R; Acquila, M; Bicocchi, Mp; Frusconi, S; Garagiola, I; Sanna, V; Santacroce, Rosa; Rocino, A; Tagariello, G. | |
Venous thrombosis in afibrinogenemia: a successful use of rivaroxaban. | 1-gen-2015 | Margaglione, M; Vecchione, G; Cappucci, F; Macarini, L; D'Andrea, G; Di Matteo, C; Grandone, E | |
Venous thrombosis in afibrinogenemia: a successful use of rivaroxaban | 1-gen-2015 | Margaglione, Maurizio; Vecchione, G; Cappucci, F; Macarini, Luca; D'Andrea, Giovanna; Di Matteo, C; Grandone, E. |
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