Sfoglia per Rivista
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women.
2014-01-01 Biguzzi, E; Franchi, F; Acaia, B; Ossola, W; Nava, U; Paraboschi, Em; Asselta, R; Peyvandi, F.
Genetic defects in congenital afibrinogenemia
2002-01-01 Asselta, R; Spena, S; Duga, S; Tenchini, Ml
Genetic diagnosis of haemophilia and other inherited bleeding disorders
2006-01-01 Peyvandi, F; Jayandharan, G; Chandy, M; Srivastava, A; Nakaya, Sm; Johnson, Mj; Thompson, Ar; Goodeve, A; Garagiola, I; Lavoretano, S; Menegatti, M; Palla, R; Spreafico, M; Tagliabue, L; Asselta, R; Duga, S; Mannucci, Pm
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay.
2015-01-01 Nuzzo, F; Paraboschi, Em; Straniero, L; Pavlova, A; Duga, S; Castoldi, E.
Identification of the first missense mutation in the fibrinogen Aalpha-chain gene in a case of afibrinogenemia
2006-01-01 Asselta, R; Platè, M; Santagostino, E; Malcovati, M; Tenchini, Ml.; Duga, S
Identification of two novel missense mutations causing factor XI deficiency
2006-01-01 Duga, S; Asselta, R; Spena, S; Tagliaferri, A; Malcovati, M; Tenchini, Ml; Castaman, G
Molecular characterization of three novel splicing mutations causing severe factor V deficiency
2006-01-01 Asselta, R; Dall’Osso, C; Duga, S; Peyvandi, F; Malcovati, M; Tenchini, Ml
Molecular investigation of 41 patients affected by coagulation factor XI deficiency
2018-01-01 Rimoldi, V; Paraboschi, E; Menegatti, M; Peyvandi, F; Salomon, O; Duga, S; Asselta, R.
Mortality and causes of death in Italian persons with haemophilia, 1990-2007
2010-01-01 Tagliaferri, A.; Rivolta, G. F.; Iorio, A.; Oliovecchio, E.; Mancuso, M. E.; Morfini, M.; Rocino, A.; Mazzucconi, M. G.; Franchini, M.; Ciavarella, N.; Scaraggi, A.; Valdrè, L.; Tagariello, G.; Radossi, P.; Muleo, G.; Iannaccaro, P. G.; Biasoli, C.; Vincenzi, D.; Serino, M. L.; Linari, S.; Molinari, C.; Boeri, E.; La Pecorella, M.; Carloni, M. T.; Santagostino, E.; Di Minno, G.; Coppola, A.; Rocino, A.; Zanon, E.; Spiezia, L.; Di Perna, C.; Marchesini, M.; Marcucci, M.; Dragani, A.; Macchi, S.; Albertini, P.; D'Incà, M.; Santoro, C.; Biondo, F.; Piseddu, G.; Rossetti, G.; Barillari, G.; Gandini, G.; Giuffrida, A. C.; Castaman, G.
Non-severe haemophilia: Is it benign? - Insights from the PROBE study
2021-01-01 Chai-Adisaksopha, C; Noone, D; Curtis, R; Frick, N; Nichol, Mb; Germini, F; O'Mahony, B; Page, D; Stonebraker, Js; Skinner, Mw; Iorio, A
Outcomes for studies assessing the efficacy of hemostatic therapies in persons with congenital bleeding disorders
2021-01-01 Aquino, Cc; Debono, Vb; Germini, F; Pete, D; Kempton, Cl; Young, G; Sidonio, R; Croteau, Se; Dunn, Al; Key, Ns; Iorio, A
Patient data meta-analysis of Post-Authorization Safety Surveillance (PASS) studies of haemophilia A patients treated with rAHF-PFM
2014-01-01 Iorio, A.; Marcucci, M.; Cheng, J.; Oldenburg, J.; Schoenig Diesing, C.; Matovinovic, E.; Romanov, V.; Thabane, L.
Rare coagulation deficiencies
2002-01-01 Peyvandi, F; Duga, S; Akhavan, S; Mannucci, Pm
Relationship of EQ-5D Pain Domain and Bleeds - Insights from the PROBE Study
2021-01-01 Skinner, M; Noone, D; Curtis, R; Frick, N; Germini, F; Kucher, A; Nichol, M; O'Mahony, B; Page, D; Stonebraker, J; Iorio, A
State of the art of rare bleeding disorders database (RBDD)
2008-01-01 Spreafico, M.; Menegatti, M.; Palla, R.; Garagiola, I.; Tagliabue, L.; Cairo, A.; Lavoretano, S.; Asselta, R.; Duga, S.; Mannucci, P. M.; Peyvandi, F.
Test-retest reliability of a mobile application of the patient reported outcomes burdens and experiences (PROBE) study
2024-01-01 Curtis, Randall; Wu, Joanne; Iorio, Alfonso; Frick, Neil; Nichol, Michael; Noone, Declan; O'Mahony, Brian; Page, David; Stonebraker, Jeffrey; Kucher, Alexandra; Clearfield, Elizabeth; Skinner, Mark W; Germini, Federico
The spectrum of FXI deficiency in Italy
2014-01-01 Castaman, G; Giacomelli, Sh; Caccia, S; Riccardi, F; Rossetti, G; Dragani, A; Giuffrida, Ac; Biasoli, C; Duga, S
Two novel homozygous mutations in the fibrinogen genes identified in two Iranian afibrinogenemic patients
2006-01-01 Monaldini, L; Duga, S; Asselta, R; Peyvandi, F; Karimi, M; Malcovati, M; Tenchini, Ml
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Genetic background and risk of postpartum haemorrhage: results from an Italian cohort of 3219 women. | 1-gen-2014 | Biguzzi, E; Franchi, F; Acaia, B; Ossola, W; Nava, U; Paraboschi, Em; Asselta, R; Peyvandi, F. | |
Genetic defects in congenital afibrinogenemia | 1-gen-2002 | Asselta, R; Spena, S; Duga, S; Tenchini, Ml | |
Genetic diagnosis of haemophilia and other inherited bleeding disorders | 1-gen-2006 | Peyvandi, F; Jayandharan, G; Chandy, M; Srivastava, A; Nakaya, Sm; Johnson, Mj; Thompson, Ar; Goodeve, A; Garagiola, I; Lavoretano, S; Menegatti, M; Palla, R; Spreafico, M; Tagliabue, L; Asselta, R; Duga, S; Mannucci, Pm | |
Identification of a novel large deletion in a patient with severe factor V deficiency using an in-house F5 MLPA assay. | 1-gen-2015 | Nuzzo, F; Paraboschi, Em; Straniero, L; Pavlova, A; Duga, S; Castoldi, E. | |
Identification of the first missense mutation in the fibrinogen Aalpha-chain gene in a case of afibrinogenemia | 1-gen-2006 | Asselta, R; Platè, M; Santagostino, E; Malcovati, M; Tenchini, Ml.; Duga, S | |
Identification of two novel missense mutations causing factor XI deficiency | 1-gen-2006 | Duga, S; Asselta, R; Spena, S; Tagliaferri, A; Malcovati, M; Tenchini, Ml; Castaman, G | |
Molecular characterization of three novel splicing mutations causing severe factor V deficiency | 1-gen-2006 | Asselta, R; Dall’Osso, C; Duga, S; Peyvandi, F; Malcovati, M; Tenchini, Ml | |
Molecular investigation of 41 patients affected by coagulation factor XI deficiency | 1-gen-2018 | Rimoldi, V; Paraboschi, E; Menegatti, M; Peyvandi, F; Salomon, O; Duga, S; Asselta, R. | |
Mortality and causes of death in Italian persons with haemophilia, 1990-2007 | 1-gen-2010 | Tagliaferri, A.; Rivolta, G. F.; Iorio, A.; Oliovecchio, E.; Mancuso, M. E.; Morfini, M.; Rocino, A.; Mazzucconi, M. G.; Franchini, M.; Ciavarella, N.; Scaraggi, A.; Valdrè, L.; Tagariello, G.; Radossi, P.; Muleo, G.; Iannaccaro, P. G.; Biasoli, C.; Vincenzi, D.; Serino, M. L.; Linari, S.; Molinari, C.; Boeri, E.; La Pecorella, M.; Carloni, M. T.; Santagostino, E.; Di Minno, G.; Coppola, A.; Rocino, A.; Zanon, E.; Spiezia, L.; Di Perna, C.; Marchesini, M.; Marcucci, M.; Dragani, A.; Macchi, S.; Albertini, P.; D'Incà, M.; Santoro, C.; Biondo, F.; Piseddu, G.; Rossetti, G.; Barillari, G.; Gandini, G.; Giuffrida, A. C.; Castaman, G. | |
Non-severe haemophilia: Is it benign? - Insights from the PROBE study | 1-gen-2021 | Chai-Adisaksopha, C; Noone, D; Curtis, R; Frick, N; Nichol, Mb; Germini, F; O'Mahony, B; Page, D; Stonebraker, Js; Skinner, Mw; Iorio, A | |
Outcomes for studies assessing the efficacy of hemostatic therapies in persons with congenital bleeding disorders | 1-gen-2021 | Aquino, Cc; Debono, Vb; Germini, F; Pete, D; Kempton, Cl; Young, G; Sidonio, R; Croteau, Se; Dunn, Al; Key, Ns; Iorio, A | |
Patient data meta-analysis of Post-Authorization Safety Surveillance (PASS) studies of haemophilia A patients treated with rAHF-PFM | 1-gen-2014 | Iorio, A.; Marcucci, M.; Cheng, J.; Oldenburg, J.; Schoenig Diesing, C.; Matovinovic, E.; Romanov, V.; Thabane, L. | |
Rare coagulation deficiencies | 1-gen-2002 | Peyvandi, F; Duga, S; Akhavan, S; Mannucci, Pm | |
Relationship of EQ-5D Pain Domain and Bleeds - Insights from the PROBE Study | 1-gen-2021 | Skinner, M; Noone, D; Curtis, R; Frick, N; Germini, F; Kucher, A; Nichol, M; O'Mahony, B; Page, D; Stonebraker, J; Iorio, A | |
State of the art of rare bleeding disorders database (RBDD) | 1-gen-2008 | Spreafico, M.; Menegatti, M.; Palla, R.; Garagiola, I.; Tagliabue, L.; Cairo, A.; Lavoretano, S.; Asselta, R.; Duga, S.; Mannucci, P. M.; Peyvandi, F. | |
Test-retest reliability of a mobile application of the patient reported outcomes burdens and experiences (PROBE) study | 1-gen-2024 | Curtis, Randall; Wu, Joanne; Iorio, Alfonso; Frick, Neil; Nichol, Michael; Noone, Declan; O'Mahony, Brian; Page, David; Stonebraker, Jeffrey; Kucher, Alexandra; Clearfield, Elizabeth; Skinner, Mark W; Germini, Federico | |
The spectrum of FXI deficiency in Italy | 1-gen-2014 | Castaman, G; Giacomelli, Sh; Caccia, S; Riccardi, F; Rossetti, G; Dragani, A; Giuffrida, Ac; Biasoli, C; Duga, S | |
Two novel homozygous mutations in the fibrinogen genes identified in two Iranian afibrinogenemic patients | 1-gen-2006 | Monaldini, L; Duga, S; Asselta, R; Peyvandi, F; Karimi, M; Malcovati, M; Tenchini, Ml |
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